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The Empirical Reality: How to Calmly Communicate the Science of modRNA Injections

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The Empirical Reality: How to Calmly Communicate the Science of modRNA Injections

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The Empirical Reality: How to Calmly Communicate the Science of modRNA Injections

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How to use peer-reviewed data and methodical authority to open minds, dismantle corporate narratives, and protect the vaccine-injured.

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Collection for UV-Microscopy - If we find a positive hit for any unusual items, receive the results from Dr. McCairn Read more…

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What We Now Know About COVID Vaccine Shedding

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Numerous data sources have corroborated that the COVID vaccines shed in a consistent and replicable manner

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Even as we enter 2026, millions of people around the world still have the COVID spike protein in their body. This isn't up for debate. It's been confirmed. Feel free to check for yourself.

The most sensitive test is by LabCorp, it is called: SARS-CoV-2 Semi-Quantitative Total Antibody, Spike. Test code is 164090. The good thing about this test is that it is very sensitive and actually gives you the exact number of COVID spike protein antibodies in your body. The test takes about 1-3 day to return, which is pretty quickly.

Many people get it checked from Quest, called: SARS COV 2 AB, TOTAL SPIKE SEMI QN, but the problem is that the Quest test maxes out it's value at 2,500. So it does not register a value over 2,500, it just says 'over 2,500.' The majority of people who had COVID, and everyone who had at least 1 vaccine will likely still be over 2,500. So doing the test with Quest is not sensitive enough.

What if they have 10,000 U/ml? 20,000 U/ml? There's no way to know if they draw the blood with Quest, that's why I prefer LabCorp because it actually gives an exact number.

Supplement / Dose Brands (we have had best luck with)

Start with 2 supplements for 1 month. In month 2, start another 2, and continue until you have completed at least 6. You can also consider starting 'Spike Support' from The Wellness Company which has some other supplements that seem to be effective for many people.

Notes:

- You can also consider exchanging Nattokinase for Lumbrokinase, I've had great success with Boluke.

- Methylene Blue has several contraindications, please look into this medication before considering.

- BPC-157 is a peptide and is on the banned list by several professional sports organizations.

- What else works?
This list is NOT comprehensive and there are other possible treatments not listed here.

# data[].attributes.attachment_link.description
Even as we enter 2026, millions of people around the world still have the COVID spike protein in their body.

# data[].attributes.attachment_link.readable_text
Even as we enter 2026, millions of people around the world still have the COVID spike protein in their body. This isn't up for debate. It's been confirmed. Feel free to check for yourself.

The most sensitive test is by LabCorp, it is called: SARS-CoV-2 Semi-Quantitative Total Antibody, Spike. Test code is 164090. The good thing about this test is that it is very sensitive and actually gives you the exact number of COVID spike protein antibodies in your body. The test takes about 1-3 day to return, which is pretty quickly.

Many people get it checked from Quest, called: SARS COV 2 AB, TOTAL SPIKE SEMI QN, but the problem is that the Quest test maxes out it's value at 2,500. So it does not register a value over 2,500, it just says 'over 2,500.' The majority of people who had COVID, and everyone who had at least 1 vaccine will likely still be over 2,500. So doing the test with Quest is not sensitive enough.

What if they have 10,000 U/ml? 20,000 U/ml? There's no way to know if they draw the blood with Quest, that's why I prefer LabCorp because it actually gives an exact number.

Supplement / Dose Brands (we have had best luck with)

Start with 2 supplements for 1 month. In month 2, start another 2, and continue until you have completed at least 6. You can also consider starting 'Spike Support' from The Wellness Company which has some other supplements that seem to be effective for many people.

Notes:

- You can also consider exchanging Nattokinase for Lumbrokinase, I've had great success with Boluke.

- Methylene Blue has several contraindications, please look into this medication before considering.

- BPC-157 is a peptide and is on the banned list by several professional sports organizations.

- What else works?
This list is NOT comprehensive and there are other possible treatments not listed here.

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Even as we enter 2026, millions of people around the world still have the COVID spike protein in their body.

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https://www.functionhealth.com/

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What We’ve Learned from a Year of Vaccine Shedding Data

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Numerous data sources now corroborate that the COVID vaccines shed in a consistent and replicable manner

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When the Vaccinated Body Becomes the Broadcast Tower: The Shedding Paradox

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Part III in our “Poisoned Not Infected” series.

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Millions Experienced COVID-19 Vaccine Side Effects

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More than a third of Americans who were vaccinated against COVID-19 say they had side effects from the shot, and nearly half suspect the vaccines killed many patients,

# data[].attributes.wish_content.attachment_props.referenced_tweets[].text
Millions Experienced COVID-19 Vaccine Side Effects

More than a third of Americans who were vaccinated against COVID-19 say they had side effects from the shot, and nearly half suspect the vaccines killed many patients. Full story is in the comments... https://t.co/MaN2ys7bEB

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FULL STORY: https://t.co/5IxaAtIebQ
— Rasmussen Reports (@Rasmussen_Poll) November 21, 2025

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Millions Experienced COVID-19 Vaccine Side Effects

# data[].attributes.attachment_link.metadata.attachment_props_source.data.entities.urls[].description
More than a third of Americans who were vaccinated against COVID-19 say they had side effects from the shot, and nearly half suspect the vaccines killed many patients,

# data[].attributes.attachment_link.metadata.attachment_props_source.includes.tweets[].text
Millions Experienced COVID-19 Vaccine Side Effects

More than a third of Americans who were vaccinated against COVID-19 say they had side effects from the shot, and nearly half suspect the vaccines killed many patients. Full story is in the comments... https://t.co/MaN2ys7bEB

# data[].attributes.attachment_link.metadata.attachment_props.entities.urls[].title
Millions Experienced COVID-19 Vaccine Side Effects

# data[].attributes.attachment_link.metadata.attachment_props.entities.urls[].description
More than a third of Americans who were vaccinated against COVID-19 say they had side effects from the shot, and nearly half suspect the vaccines killed many patients,

# data[].attributes.attachment_link.metadata.attachment_props.referenced_tweets[].text
Millions Experienced COVID-19 Vaccine Side Effects

More than a third of Americans who were vaccinated against COVID-19 say they had side effects from the shot, and nearly half suspect the vaccines killed many patients. Full story is in the comments... https://t.co/MaN2ys7bEB

# data[].attributes.wish_content.attachment_props.text
DARPA’s Secret 60-Day Pandemic Pipeline: FOIA Documents Reveal U.S. Military Program to Synthesize Viruses From Digital Sequences and Mass-Produce mRNA Countermeasures

Newly released DARPA files show a Pentagon-backed system designed to turn raw genetic code into real viruses, https://t.co/RKByE7c5en

# data[].attributes.wish_content.attachment_props.original_text
DARPA’s Secret 60-Day Pandemic Pipeline: FOIA Documents Reveal U.S. Military Program to Synthesize Viruses From Digital Sequences and Mass-Produce mRNA Countermeasures

Newly released DARPA files show a Pentagon-backed system designed to turn raw genetic code into real viruses, https://t.co/RKByE7c5en

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DARPA’s Secret 60-Day Pandemic Pipeline: FOIA Documents Reveal U.S. Military Program to Synthesize Viruses From Digital Sequences and Mass-Produce mRNA Countermeasures

Newly released DARPA files show a Pentagon-backed system designed to turn raw genetic code into real viruses,… pic.twitter.com/RKByE7c5en
— Jon Fleetwood (@JonMFleetwood) November 19, 2025

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DARPA’s Secret 60-Day Pandemic Pipeline: FOIA Documents Reveal U.S. Military Program to Synthesize Viruses From Digital Sequences and Mass-Produce mRNA Countermeasures

Newly released DARPA files show a Pentagon-backed system designed to turn raw genetic code into real viruses, https://t.co/RKByE7c5en

# data[].attributes.attachment_link.metadata.attachment_props.original_text
DARPA’s Secret 60-Day Pandemic Pipeline: FOIA Documents Reveal U.S. Military Program to Synthesize Viruses From Digital Sequences and Mass-Produce mRNA Countermeasures

Newly released DARPA files show a Pentagon-backed system designed to turn raw genetic code into real viruses, https://t.co/RKByE7c5en

# data[].attributes.attachment_link.metadata.attachment_props.text
DARPA’s Secret 60-Day Pandemic Pipeline: FOIA Documents Reveal U.S. Military Program to Synthesize Viruses From Digital Sequences and Mass-Produce mRNA Countermeasures

Newly released DARPA files show a Pentagon-backed system designed to turn raw genetic code into real viruses, https://t.co/RKByE7c5en

# data[].attributes.wish_content.attachment_props.text
NBC today blasted @realDonaldTrump and @RobertKennedyJr for wanting to study a possible connection between "autism and childhood vaccines" because NBC claims it has been "debunked" by "hundreds of studies."** But has it? The answer is unmistakably "no!" Here is the proof:

Most

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NBC today blasted @realDonaldTrump and @RobertKennedyJr for wanting to study a possible connection between "autism and childhood vaccines" because NBC claims it has been "debunked" by "hundreds of studies."** But has it? The answer is unmistakably "no!" Here is the proof:

Most

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NBC today blasted @realDonaldTrump and @RobertKennedyJr for wanting to study a possible connection between "autism and childhood vaccines" because NBC claims it has been "debunked" by "hundreds of studies."** But has it? The answer is unmistakably "no!" Here is the proof:

Most…
— Aaron Siri (@AaronSiriSG) December 8, 2024

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NBC today blasted @realDonaldTrump and @RobertKennedyJr for wanting to study a possible connection between "autism and childhood vaccines" because NBC claims it has been "debunked" by "hundreds of studies."** But has it? The answer is unmistakably "no!" Here is the proof:

Most

# data[].attributes.attachment_link.metadata.attachment_props.original_text
NBC today blasted @realDonaldTrump and @RobertKennedyJr for wanting to study a possible connection between "autism and childhood vaccines" because NBC claims it has been "debunked" by "hundreds of studies."** But has it? The answer is unmistakably "no!" Here is the proof:

Most

# data[].attributes.attachment_link.metadata.attachment_props.text
NBC today blasted @realDonaldTrump and @RobertKennedyJr for wanting to study a possible connection between "autism and childhood vaccines" because NBC claims it has been "debunked" by "hundreds of studies."** But has it? The answer is unmistakably "no!" Here is the proof:

Most

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PLAGUE of CORRUPTION - Liam Neeson Narrates the Investigation - 80 years of Deception

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The most puzzling part of the COVID vaccine is its ability to "shed" and harm those who never got it. A peer-reviewed study just validated the thousands of shedding reports I've evaluated here.

Please share your story so we can untangle this mystery.
https://t.co/6KaqiT31Cb

# data[].attributes.wish_content.attachment_props.entities.urls[].title
What We've Learned from a Year of Vaccine Shedding Data

# data[].attributes.wish_content.attachment_props.entities.urls[].description
Numerous data sources now corroborate that the COVID vaccines shed in a consistent and replicable manner

# data[].attributes.wish_content.attachment_props.original_text
The most puzzling part of the COVID vaccine is its ability to "shed" and harm those who never got it. A peer-reviewed study just validated the thousands of shedding reports I've evaluated here.

Please share your story so we can untangle this mystery.
https://t.co/6KaqiT31Cb

# data[].attributes.attachment_link.embed_code
The most puzzling part of the COVID vaccine is its ability to "shed" and harm those who never got it. A peer-reviewed study just validated the thousands of shedding reports I've evaluated here.

Please share your story so we can untangle this mystery.https://t.co/6KaqiT31Cb
— A Midwestern Doctor (@MidwesternDoc) November 15, 2025

# data[].attributes.attachment_link.metadata.attachment_props_source.data.entities.urls[].title
What We've Learned from a Year of Vaccine Shedding Data

# data[].attributes.attachment_link.metadata.attachment_props_source.data.entities.urls[].description
Numerous data sources now corroborate that the COVID vaccines shed in a consistent and replicable manner

# data[].attributes.attachment_link.metadata.attachment_props_source.data.text
The most puzzling part of the COVID vaccine is its ability to "shed" and harm those who never got it. A peer-reviewed study just validated the thousands of shedding reports I've evaluated here.

Please share your story so we can untangle this mystery.
https://t.co/6KaqiT31Cb

# data[].attributes.attachment_link.metadata.attachment_props.original_text
The most puzzling part of the COVID vaccine is its ability to "shed" and harm those who never got it. A peer-reviewed study just validated the thousands of shedding reports I've evaluated here.

Please share your story so we can untangle this mystery.
https://t.co/6KaqiT31Cb

# data[].attributes.attachment_link.metadata.attachment_props.text
The most puzzling part of the COVID vaccine is its ability to "shed" and harm those who never got it. A peer-reviewed study just validated the thousands of shedding reports I've evaluated here.

Please share your story so we can untangle this mystery.
https://t.co/6KaqiT31Cb

# data[].attributes.attachment_link.metadata.attachment_props.entities.urls[].title
What We've Learned from a Year of Vaccine Shedding Data

# data[].attributes.attachment_link.metadata.attachment_props.entities.urls[].description
Numerous data sources now corroborate that the COVID vaccines shed in a consistent and replicable manner

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https://sayerji.substack.com/p/follow-the-silenced-world-premiere

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https://greenmedinfo.com/

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🚨 Louisiana has made history! 

HB690 has been signed into law, making Louisiana the first state to establish formal rules for the administration of EUA products—including informed consent protections.

This is a major step forward for patient rights and medical ethics.

Huge https://t.co/0sVeJgkrk2

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🚨 Louisiana has made history! 

HB690 has been signed into law, making Louisiana the first state to establish formal rules for the administration of EUA products—including informed consent protections.

This is a major step forward for patient rights and medical ethics.

Huge https://t.co/0sVeJgkrk2

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🚨 Louisiana has made history!

HB690 has been signed into law, making Louisiana the first state to establish formal rules for the administration of EUA products—including informed consent protections.

This is a major step forward for patient rights and medical ethics.

Huge… pic.twitter.com/0sVeJgkrk2
— Health Freedom Louisiana (@HealthFreedomLA) June 26, 2025

# data[].attributes.attachment_link.metadata.attachment_props_source.data.text
🚨 Louisiana has made history! 

HB690 has been signed into law, making Louisiana the first state to establish formal rules for the administration of EUA products—including informed consent protections.

This is a major step forward for patient rights and medical ethics.

Huge https://t.co/0sVeJgkrk2

# data[].attributes.attachment_link.metadata.attachment_props.original_text
🚨 Louisiana has made history! 

HB690 has been signed into law, making Louisiana the first state to establish formal rules for the administration of EUA products—including informed consent protections.

This is a major step forward for patient rights and medical ethics.

Huge https://t.co/0sVeJgkrk2

# data[].attributes.attachment_link.metadata.attachment_props.text
🚨 Louisiana has made history! 

HB690 has been signed into law, making Louisiana the first state to establish formal rules for the administration of EUA products—including informed consent protections.

This is a major step forward for patient rights and medical ethics.

Huge https://t.co/0sVeJgkrk2

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They Don’t Just Harm You — They May Harm Others Too 👇

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COVID-19 mRNA Shots Shed. 

They Don’t Just Harm You — They May Harm Others Too 👇 https://t.co/PhsgzabVfU https://t.co/olOwk2Osk3

# data[].attributes.wish_content.attachment_props.original_text
COVID-19 mRNA Shots Shed. 

They Don’t Just Harm You — They May Harm Others Too 👇 https://t.co/PhsgzabVfU https://t.co/olOwk2Osk3

# data[].attributes.wish_content.attachment_props.referenced_tweets[].text
mRNA injections shed and therefore violate the bodily autonomy of innocent bystanders.

Peters et al found that women with daily close proximity (within 6 feet) to vaccinated individuals outside their household had significant menstrual abnormalities:

📈 34% higher risk of https://t.co/rPjytJVCQ1 https://t.co/ppANKEHX2A

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COVID-19 mRNA Shots Shed.

They Don’t Just Harm You — They May Harm Others Too 👇 https://t.co/olOwk2Osk3 pic.twitter.com/PhsgzabVfU
— Nicolas Hulscher, MPH (@NicHulscher) June 25, 2025

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COVID-19 mRNA Shots Shed. 

They Don’t Just Harm You — They May Harm Others Too 👇 https://t.co/PhsgzabVfU https://t.co/olOwk2Osk3

# data[].attributes.attachment_link.metadata.attachment_props_source.includes.tweets[].text
mRNA injections shed and therefore violate the bodily autonomy of innocent bystanders.

Peters et al found that women with daily close proximity (within 6 feet) to vaccinated individuals outside their household had significant menstrual abnormalities:

📈 34% higher risk of https://t.co/rPjytJVCQ1 https://t.co/ppANKEHX2A

# data[].attributes.attachment_link.metadata.attachment_props.original_text
COVID-19 mRNA Shots Shed. 

They Don’t Just Harm You — They May Harm Others Too 👇 https://t.co/PhsgzabVfU https://t.co/olOwk2Osk3

# data[].attributes.attachment_link.metadata.attachment_props.text
COVID-19 mRNA Shots Shed. 

They Don’t Just Harm You — They May Harm Others Too 👇 https://t.co/PhsgzabVfU https://t.co/olOwk2Osk3

# data[].attributes.attachment_link.metadata.attachment_props.referenced_tweets[].text
mRNA injections shed and therefore violate the bodily autonomy of innocent bystanders.

Peters et al found that women with daily close proximity (within 6 feet) to vaccinated individuals outside their household had significant menstrual abnormalities:

📈 34% higher risk of https://t.co/rPjytJVCQ1 https://t.co/ppANKEHX2A

# data[].attributes.wish_content.attachment_props.text
BREAKING : now in peer reviewed journal: 

A stunning 33% reduction in the rate of successful conceptions among vaccinated women compared to unvaccinated women.

https://t.co/jObh1w82TU

# data[].attributes.wish_content.attachment_props.entities.urls[].title
Rates of successful conceptions according to COVID-19 vaccination status: Data from the Czech Republic - Vibeke Manniche, Tomáš Fürst, Max Schmeling, Jonathan D Gilthorpe, Peter Riis Hansen, 2025

# data[].attributes.wish_content.attachment_props.entities.urls[].description
Background Adverse effects of COVID-19 vaccination on human menstrual cycle characteristics have been observed, but limited data are available on the relationsh...

# data[].attributes.wish_content.attachment_props.original_text
BREAKING : now in peer reviewed journal: 

A stunning 33% reduction in the rate of successful conceptions among vaccinated women compared to unvaccinated women.

https://t.co/jObh1w82TU

# data[].attributes.attachment_link.embed_code
BREAKING : now in peer reviewed journal:

A stunning 33% reduction in the rate of successful conceptions among vaccinated women compared to unvaccinated women.https://t.co/jObh1w82TU
— Steve Kirsch (@stkirsch) June 24, 2025

# data[].attributes.attachment_link.metadata.attachment_props_source.data.text
BREAKING : now in peer reviewed journal: 

A stunning 33% reduction in the rate of successful conceptions among vaccinated women compared to unvaccinated women.

https://t.co/jObh1w82TU

# data[].attributes.attachment_link.metadata.attachment_props_source.data.entities.urls[].title
Rates of successful conceptions according to COVID-19 vaccination status: Data from the Czech Republic - Vibeke Manniche, Tomáš Fürst, Max Schmeling, Jonathan D Gilthorpe, Peter Riis Hansen, 2025

# data[].attributes.attachment_link.metadata.attachment_props_source.data.entities.urls[].description
Background Adverse effects of COVID-19 vaccination on human menstrual cycle characteristics have been observed, but limited data are available on the relationsh...

# data[].attributes.attachment_link.metadata.attachment_props.original_text
BREAKING : now in peer reviewed journal: 

A stunning 33% reduction in the rate of successful conceptions among vaccinated women compared to unvaccinated women.

https://t.co/jObh1w82TU

# data[].attributes.attachment_link.metadata.attachment_props.text
BREAKING : now in peer reviewed journal: 

A stunning 33% reduction in the rate of successful conceptions among vaccinated women compared to unvaccinated women.

https://t.co/jObh1w82TU

# data[].attributes.attachment_link.metadata.attachment_props.entities.urls[].title
Rates of successful conceptions according to COVID-19 vaccination status: Data from the Czech Republic - Vibeke Manniche, Tomáš Fürst, Max Schmeling, Jonathan D Gilthorpe, Peter Riis Hansen, 2025

# data[].attributes.attachment_link.metadata.attachment_props.entities.urls[].description
Background Adverse effects of COVID-19 vaccination on human menstrual cycle characteristics have been observed, but limited data are available on the relationsh...

# data[].attributes.body
https://www.thefocalpoints.com/p/17-ways-mrna-shots-may-cause-cancer

# data[].attributes.body
https://journals.sagepub.com/doi/10.1177/09246479251353384

# data[].attributes.attachment_link.title
BREAKING - Peer-Reviewed Manuscript Finds Irrefutable Evidence Supporting Immediate Market Withdrawal of COVID-19 “Vaccines”

# data[].attributes.attachment_link.description
Over 81,000 physicians, scientists, and concerned citizens, 240 elected officials, 17 professional organizations, excess mortality, negative efficacy, and DNA contamination call for urgent action.

# data[].attributes.body
https://www.medrxiv.org/content/10.1101/2025.06.18.25329352v1

Analysis of over 220K pregnancies in Israel during 2016- 2022 found that mRNA COVID-19 vaccination during gestational weeks 8-13 was associated with a higher-than-expected number of eventual fetal losses (miscarriages, abortions & stillbirths)!

# data[].attributes.body
https://www.medrxiv.org/content/10.1101/2025.06.18.25329352v1

# data[].attributes.body
https://www.nature.com/articles/s41390-025-04192-w

# data[].attributes.wish_content.attachment_props.text
COVID-19 ‘vaccines’ damage the brain and DEVASTATE mental health. They increase your risk of: 
1. Alzheimer’s (+22.5%), 
2. Cognitive impairment (+137.7%) 
3. Depression (+68.3%)
4. Anxiety disorders (+43.9%) 
5. Sleep disorders (+93.4%)  
This is likely due to toxic Spike https://t.co/rMJMzCA9bc

# data[].attributes.wish_content.attachment_props.original_text
COVID-19 ‘vaccines’ damage the brain and DEVASTATE mental health. They increase your risk of: 
1. Alzheimer’s (+22.5%), 
2. Cognitive impairment (+137.7%) 
3. Depression (+68.3%)
4. Anxiety disorders (+43.9%) 
5. Sleep disorders (+93.4%)  
This is likely due to toxic Spike https://t.co/rMJMzCA9bc

# data[].attributes.attachment_link.embed_code
COVID-19 ‘vaccines’ damage the brain and DEVASTATE mental health. They increase your risk of:
1. Alzheimer’s (+22.5%),
2. Cognitive impairment (+137.7%)
3. Depression (+68.3%)
4. Anxiety disorders (+43.9%)
5. Sleep disorders (+93.4%)
This is likely due to toxic Spike… pic.twitter.com/rMJMzCA9bc
— Nicolas Hulscher, MPH (@NicHulscher) January 4, 2025

# data[].attributes.attachment_link.metadata.attachment_props_source.data.text
COVID-19 ‘vaccines’ damage the brain and DEVASTATE mental health. They increase your risk of: 
1. Alzheimer’s (+22.5%), 
2. Cognitive impairment (+137.7%) 
3. Depression (+68.3%)
4. Anxiety disorders (+43.9%) 
5. Sleep disorders (+93.4%)  
This is likely due to toxic Spike https://t.co/rMJMzCA9bc

# data[].attributes.attachment_link.metadata.attachment_props.original_text
COVID-19 ‘vaccines’ damage the brain and DEVASTATE mental health. They increase your risk of: 
1. Alzheimer’s (+22.5%), 
2. Cognitive impairment (+137.7%) 
3. Depression (+68.3%)
4. Anxiety disorders (+43.9%) 
5. Sleep disorders (+93.4%)  
This is likely due to toxic Spike https://t.co/rMJMzCA9bc

# data[].attributes.attachment_link.metadata.attachment_props.text
COVID-19 ‘vaccines’ damage the brain and DEVASTATE mental health. They increase your risk of: 
1. Alzheimer’s (+22.5%), 
2. Cognitive impairment (+137.7%) 
3. Depression (+68.3%)
4. Anxiety disorders (+43.9%) 
5. Sleep disorders (+93.4%)  
This is likely due to toxic Spike https://t.co/rMJMzCA9bc

# data[].attributes.attachment_link.authors[].name
The Last Boomer Podcast with John Beaudoin Sr Verified 0 followers

# data[].attributes.attachment_link.title
“The Last Boomer” Podcast with John Beaudoin Sr

# data[].attributes.attachment_link.description
What really happened during covid 2020-2025)? TRUTH from official government records they do NOT want you to know.

# data[].attributes.headline
COVID-19 mRNA Shots Destroy Over 60% of Women’s Egg Supply

# data[].attributes.subject
COVID-19 mRNA Shots Destroy Over 60% of Women’s Egg Supply

# data[].attributes.body
https://www.thefocalpoints.com/p/breaking-covid-19-mrna-shots-destroy

# data[].attributes.body
http://denwalker.com/

# data[].attributes.attachment_link.title
Indian scientists had found unique ‘insertions’ in Covid-19 virus genome

# data[].attributes.attachment_link.description
Researchers from Kusuma School of Biological Sciences in IIT Delhi had found that Covid-19 virus in humans is different from those in bats

# data[].attributes.body
Spike protein-related proteinopathies: a focus on the neurological side of spikeopathies

https://www.sciencedirect.com/science/article/pii/S0940960225002894

# data[].attributes.body
https://news.rebekahbarnett.com.au/p/how-the-us-government-funded-narrative

# data[].attributes.attachment_link.title
Hundreds of Studies Show DMSO Transforms The Treatment of Cancer

# data[].attributes.attachment_link.description
A remarkable cancer treatment has been hiding in plain sight for decades

# data[].attributes.body
https://cardiovascular-research-and-innovation.reseaprojournals.com/Articles/myocarditis-after-sars-cov-2-infection-and-covid-19-vaccination-epidemiology-outcomes-and-new-perspectives

# data[].attributes.headline
‘Spikeopathy’: COVID-19 Spike Protein Is Pathogenic, from Both Virus and Vaccine mRNA

# data[].attributes.subject
‘Spikeopathy’: COVID-19 Spike Protein Is Pathogenic, from Both Virus and Vaccine mRNA

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Abstract

The COVID-19 pandemic caused much illness, many deaths, and profound disruption to society. The production of 'safe and effective' vaccines was a key public health target. Sadly, unprecedented high rates of adverse events have overshadowed the benefits. This two-part narrative review presents evidence for the widespread harms of novel product COVID-19 mRNA and adenovectorDNA vaccines and is novel in attempting to provide a thorough overview of harms arising from the new technology in vaccines that relied on human cells producing a foreign antigen that has evidence of pathogenicity. This first paper explores peer-reviewed data counter to the 'safe and effective' narrative attached to these new technologies. Spike protein pathogenicity, termed 'spikeopathy', whether from the SARS-CoV-2 virus or produced by vaccine gene codes, akin to a 'synthetic virus', is increasingly understood in terms of molecular biology and pathophysiology. Pharmacokinetic transfection through body tissues distant from the injection site by lipid-nanoparticles or viral-vector carriers means that 'spikeopathy' can affect many organs. The inflammatory properties of the nanoparticles used to ferry mRNA; N1-methylpseudouridine employed to prolong synthetic mRNA function; the widespread biodistribution of the mRNA and DNA codes and translated spike proteins, and autoimmunity via human production of foreign proteins, contribute to harmful effects. This paper reviews autoimmune, cardiovascular, neurological, potential oncological effects, and autopsy evidence for spikeopathy. With many gene-based therapeutic technologies planned, a re-evaluation is necessary and timely.

Keywords: spike protein, pathology, transfection, biodistribution, lipid-nanoparticles, autopsy, inflammation, pharmacovigilance, COVID-19, mRNA vaccines

1. Introduction

In this narrative review, we examine the solid evidence for a counter-narrative to the 'safe and effective' message that has accompanied the novel product COVID-19 vaccines, which were developed at 'warp speed' with great hope to end the pandemic. This evidence has accumulated and dampened the original optimism. The implications for the recognition of vaccine-related diagnoses and the need for therapeutics are significant for all health practitioners and many research scientists to consider.

Key problem areas appear to be (1) the toxicity of the spike protein-both from the virus and also when produced by gene codes in the novel COVID-19 mRNA and adenovectorDNA vaccines [ 1, 2], hence the novel term 'spikeopathy'; (2) inflammatory properties of certain lipid-nanoparticles used to ferry mRNA [ 3]; (3) N1-methylpseudouridine in the synthetic mRNA that causes long-lasting action [ 4]; (4) widespread biodistribution of the mRNA [ 5] and DNA [ 6, 7] codes via the lipid-nanoparticle and the viral-vector carrier matrices, respectively and (5) the problem of human cells producing a foreign protein in our ribosomes that can engender autoimmunity [ 8, 9].

The emergence of SARS-CoV-2 in late 2019, and the associated disease of COVID-19, declared by March 2020 as a global pandemic by the WHO, has caused much illness, and many deaths in the elderly and the at-risk, and seriously disrupted society. An umbrella literature review of publications between December 2019 and August 2021 revealed that the greatest risk of mortality due to COVID-19 was associated with cardiovascular disease, cerebrovascular disease, and chronic renal disease [ 10]. The production of safe and effective vaccines to halt the COVID-19 pandemic was one of the most important public health interventions. Many COVID-19 vaccines have been developed across the world. In non-Western nations, most vaccines have used traditional protein-based or inactivated virus technologies. The mRNA and adenovectorDNA vaccines have been produced by large pharmaceutical companies and favoured by regulators in most Western nations. It has been widely claimed that these vaccines have saved millions of lives. Sincere hopes have been held for this narrative. But this belief is largely founded on early Infection Fatality Rate (IFR) modelling estimates and Pfizer, Moderna, AstraZeneca and Janssen claims of efficacy, which have been undermined by new data.

Controversy has surrounded the use of the gene-based vaccines and this article explores the reason for this. To meet the widespread desire for 'safe and effective' vaccines, gene-based technology offers rapid speed of production. Hope has perhaps influenced much of the published literature as well as media narrative. A central issue has been growing evidence of pathogenic effects of the SARS-CoV-2 spike protein-whether as part of the virus or produced by genetic codes in the mRNA and adenovectorDNA vaccines.

The aim of this narrative review is to present a comprehensive account of the pathogenicity of the antigen, the biodistribution of the gene codes for the antigen throughout the body, their modified long-lasting nature particularly with the mRNA vaccines, and literature and data that show the adverse events that would be expected from such biodistribution and cellular production of a foreign antigen. The review presents a case of premature translation of experimental gene therapy technology to mass public vaccination and ethical and regulatory issues that need scrutiny and reform before the next pandemic.

Central to individual informed consent decisions and public health policy is the weighing of the risks of an illness versus the risks and potential benefits of an intervention. Given the risks of novel gene-based COVID-19 vaccines, were they worth it in light of the severity of SARS-CoV-2 infection? We address the risks of COVID-19 first.

2. COVID-19 Modelling Versus Real-World Data

It is apparent that the original Wuhan strain and early variants of SARS-CoV-2 in 2020 were more pathogenic than later variants. This is consistent with typical viral adaptive evolution to more infectious but less pathogenic strains, a natural phenomenon that is fortunate for humanity. The claim that the COVID-19 vaccines have saved many millions of lives is predicated on modelling based on case fatality rates (CFR) in China in February 2020 published by Verity et al. in The Lancet [ 11]. The authors estimated a CFR of 6.4% (5.7-7.2) in those aged over 60 years and "up to 13.4% (11.2-15.9) in those aged 80 years or older... with an overall infection fatality ratio for China of 0.66% (0.39-1.33)" (abstract). Fortunately, the virus mutated, and these modelling predictions did not materialise as the pandemic unfolded over the next three years.

The COVID-19 vaccines have saved lives from COVID-19, but it is not clear how many. The claim of millions of lives saved by COVID-19 gene-based vaccines was partly based on assumptions that the COVID-19 vaccines protected against infection and transmission, which was not the case because systemic immunity to respiratory viruses is not as effective as mucosal immunity from infection, and because of the continually evolving variants perhaps partly driven by adaptive evasion of vaccine-induced antibodies. Pfizer admitted that its phase 3 clinical trial [ 12] did not test for viral transmission [ 13].

However, presumptions of efficacy have been sustained by COVID-19 modellers, and reiterated by health authorities, medical publications, and the media. This is exhibited by Watson et al., (2022) in "Global impact of the first year of COVID-19 vaccination: a mathematical modelling study", published in The Lancet Infectious Diseases [ 14]. The authors estimate around 14.4 million lives saved related to vaccination benefits that include protection against infection and transmission, both now recognised to be unfounded. This suppositional estimate by Watson et al. persists as an accepted fact, whereas real-world infection fatality rate (IFR) data speak against the need for vaccination in the non-elderly.

Briefly, Roussel et al. in early 2020 presented a statistically significant analysis that likened the case fatality rate for SARS-CoV-2 to earlier coronaviruses and influenza-like illnesses: In OECD countries, the mortality rate for SARS-CoV-2 (1.3%) was not significantly different from that for common coronaviruses identified in public hospitals of Marseille, France (0.8%; p = 0.11) [ 15]. If modelling had been based on these data a few months after the initial Chinese data, different projections would have been made, more in line with eventual mortality statistics including in 2020 prior to any vaccine availability.

Ioannidis et al. in 2022 in a paper titled "Forecasting for COVID-19 has failed" critiqued the models that ignored the low IFRs to emerge in the first half of 2020 [ 16]. Ioannidis et al. noted:

" Failure in epidemic forecasting is an old problem. In fact, it is surprising that epidemic forecasting has retained much credibility among decision-makers, given its dubious track record. Modelling for swine flu predicted 3100-65,000 deaths in the UK (https://www.theguardian.com/uk/2009/jul/16/swine-flu-cases-rise-britain. (Accessed on 2 June 2020). Eventually, 457 deaths occurred (UK government, 2009) ".

[ 16] (p. 425)

Ioannidis et al. then examined many US COVID-19 prediction models for deaths, hospitalisations, and ICU admissions, highlighting the extremely wide margins by which they failed to hit their targets. Ioannidis et al. continued:

" Despite these obvious failures, [COVID-19] epidemic forecasting continued to thrive, perhaps because vastly erroneous predictions typically lacked serious consequences... Upon acquiring solid evidence about the epidemiological features of new outbreaks, implausible, exaggerated forecasts (Ioannidis, 2020d) should be abandoned. Otherwise, they may cause more harm than the virus itself ".

[ 16] (p. 428)

Societal narratives, once entrenched, become difficult to shift.

Accurate estimates of lives saved or lost as a result of the COVID-19 gene-based vaccines would have required long-term studies in vaccinated compared to unvaccinated individuals. Pfizer, Moderna, AstraZeneca and Janssen eventually vaccinated almost all placebo subjects and thus lost their control group. This was based on ethical principles given the fear of COVID-19 [ 17], but the loss to scientific integrity of only having short-term placebo-controlled trials was noted by the WHO Ad Hoc Expert Group on the Next Steps for Covid-19 Evaluation (2020) [ 18].

To make up this deficit, one private organisation based in the UK, Control Group Cooperative [ 19], has collected data since the COVID-19 vaccination rollout, and is the only world-wide control group. Of this unvaccinated cohort 18,497 participated in a survey reporting COVID-19 positive testing and symptom severity between September 2021 and February 2022. A quarter (4636, 25.1%) reported experiencing symptomatic COVID-19 illness. Symptoms were reported as "mild" by 14.4%, "moderate" by 8.7% and "severe" by 2%. A further 560 reported asymptomatic illness and of the 5196 with COVID-19, only 74 (1.4%) reported attending hospital (as in- or out-patients) with 21 (0.4%) being hospitalised for longer than 1 week. As a self-reported survey, the limitations included deaths that may not have been reported; nonetheless, the cohort fared better than expected. The group was perhaps unusual in that 71% partook of some combination of vitamins C, D, quercetin, zinc and off-label ivermectin or hydroxychloroquine where available [ 20].

In this context, the Australian State Government (NSW) health data from November and December 2022 [ 21] ( Figure 1 and Figure 2) demonstrate that the unvaccinated are almost not represented in the hospitalisation data while the most vaccinated are over-represented. The proportion of unvaccinated in NSW was low at 3.2%; however, the proportion of unvaccinated with severe COVID-19 is lower than this in late 2022 at 2.9%. Even accounting for more COVID-19 vaccine boosters in the elderly and vulnerable, the data do not suggest significant efficacy against hospitalisation, ICU admission and death, at least after the emergence of the Omicron strain.

Figure 1.

NSW Australia hospitalisations, ICU admissions and deaths last 6 weeks 2022 by vaccination status. NSW Health. Bar charts derived from the numbers in official government report excerpt of posted as Figure 2 [ 21].

Figure 2.

NSW Australia COVID-19 hospitalisations, ICU admissions, deaths, last 2 weeks 2022. NSW Health. From Table 1 of NSW Covid weekly data overview last 2 weeks 2022. Note that regional councils analysis of same data removed for space reasons. Used under Creative Commons Attribution 4.0 license. © State of New South Wales. For current information go to www.nsw.gov.au. [ 21].

For weeks 51 and 52 of 2022, the NSW government data document nil hospitalisations and six deaths for unvaccinated persons, but 1415 hospitalisations and 82 deaths in known vaccinated persons. NSW Health no longer publishes vaccination status. These data do not support the premise that the vaccinations have 'saved millions of lives', but instead indicate correlations between more doses with severe COVID-19 illness warrants investigation. There has been an increase in all-cause mortality contemporaneous with the rollout of the COVID-19 gene-based vaccines and this warrants further research.

Mathematical models produce highly uncertain numbers that predict the future. These predictions can become politicised. To make sure predictions do not become adjuncts to a political cause, modellers, decision-makers and citizens need to establish the real-world facts that hold us all accountable.

If the COVID-19 vaccines are less efficacious than was originally hoped for and subsequently claimed, then the risk/benefit decision-making for individual informed consent and public health policy shifts. The degree of harm caused by the novel gene-based vaccine technology might then outweigh any benefits.

3. Correspondence between TGA and Australian Senator Rennick

In Australia, the Therapeutic Goods Administration (TGA) provisionally approved the COVID-19 vaccines of Pfizer (Comirnaty, BNT162b2), Moderna (SPIKEVAX, mRNA-1273), AstraZeneca (Vaxzevria, ChAdOx1 nCOV-19) and Janssen (COVID-19 Vaccine, Ad26.COV2.S) in early 2021 [ 22] and in January 2022 added the protein-based lipid-nanoparticle embedded vaccine of Novavax (Nuvaxovid, NVX-CoV2373) [ 23].

On 16 December 2022, the Australian Department of Health advised by the TGA responded to Question 235 from 21 November 2022 by Senator Gerard Rennick (Liberal Party, Qld) in the Senate Community Affairs Committee Question on Notice SQ22-000609. Senator Rennick, whose parliamentary office has received numerous accounts of COVID-19 vaccine injuries from Australians, had asked whether the TGA's own report [ 5] that showed widely biodistributed high transfection and expression rates of the gene-based COVID-19 mRNA vaccines, was proof the vaccines were more pathogenic than the virus, implying more spike protein load on human cells [ 24].

The TGA replied:

" There is some confusion around the biochemistry and immunology here. Higher translation and expression rate is not associated with pathogenicity, rather it indicates better antigen (spike protein) expression. The expressed spike protein is not a pathogen and is not infectious. The spike protein is only one component of the coronavirus. It serves as an antigen to induce humoral and cellular immune responses against SARS-CoV-2 virus ".

[ 24]

As Australian authors of this paper, we concur with the opinion of the TGA that the spike protein produced by the gene-based COVID-19 vaccines does act as an antigen to induce immune responses and is not a whole microorganism pathogen. However, the response by the TGA has missed the point of the question. We will summarise the evidence that the spike protein itself is independently bioactive and pathogenic. The spike protein has been directly related to both the pathophysiology that underlies COVID-19 viral illness and the serious adverse events from the COVID-19 vaccines that, via gene therapy mechanisms, induce human cells to produce the spike protein in substantial numbers.

In fact, the spike protein in the original SARS coronavirus 1 (SARS CoV-1) epidemic in 2003 was identified as a cause of lung injury for which the term 'severe acute respiratory syndrome' (SARS) was coined. It was thought to do this via action on angiotensin-converting enzyme 2 (ACE-2) receptors. SARS-CoV-1 (2003 virus) spike protein-driven downregulation of ACE-2 receptors led to lung oedema and acute pulmonary failure in mice as published in Nature Medicine [ 25].

4. Narrative Review Methodology

We present here a narrative review of the literature that provides evidence for the toxicity and thus pathogenicity of the spike protein, independent of its role as a pathogenic determinant in SARS-CoV-2 infection. This is whether from the SARS-CoV-2 virus or produced by genetic code in human cells directly by mRNA (Pfizer and Moderna) or by mRNA derived from the adenovectorDNA (AstraZeneca and Janssen) COVID-19 vaccines.

We also review literature evidence for the toxicity and biodistribution profile of concern for the lipid-nanoparticle matrices for mRNA Moderna and Pfizer and protein-based Novavax COVID-19 vaccines; the modified nature of the synthetic mRNA which would explain prolonged mRNA persistence and spike protein production; the phenomenon of 'bad batch' variation in adverse event reports and relevant age-stratified risk/benefit considerations for COVID-19 vaccinations especially for paediatric and younger adult age cohorts.

These pharmacokinetic and pharmacodynamic aspects relate to the pathogenicity of the gene-based COVID-19 vaccines. In the context of the TGA's reply above, the pharmacokinetic biodistribution aspects of the gene-based COVID-19 vaccines are akin to an 'infectious' agent, in an invasive or blood-borne phase, as they distribute the pathogenic effects of the spike protein throughout the body.

This review presents evidence from the academic literature, as well as pharmacovigilance, and Pfizer clinical trial documents, via Freedom of Information (FOI) orders, to assist the TGA and other regulators and health authorities in reappraising the toxicity of the mRNA and adenovectorDNA produced spike proteins. A new era of pathology is emerging that could be termed "Spikeopathy". It is also vital to evaluate the potential for any new autoimmune phenomena driven by foreign antigen production caused by any new mRNA or DNA-based technology in the future.

Evidence for harm caused by 'spikeopathy', as well as other forms of pathophysiological damage, are reviewed by organ system, while a review of pharmacovigilance data will be the subject of a further paper.

The Key Points below summarise the information presented.

Key Points

Highly safe and effective vaccines are central to combat infectious disease epidemics/pandemics.

SARS-CoV-2 spike protein is pathogenic, whether from the virus or created from genetic code in mRNA and adenovectorDNA vaccines.

Biodistribution rodent study data show lipid nanoparticles carry mRNA to all organs and cross blood-brain and blood-placenta barriers. Some of these tissues are likely to be impervious to viral infection; therefore, the biohazard is particularly from vaccination.

Lipid-nanoparticles have inflammatory properties.

The modification of mRNA with N1-methylpseudouridine for increased stability leads to the production of spike proteins for months. It is uncertain how many cells and from which organs mRNA spike proteins are produced, and therefore, the exact effective dose delivered per vaccine vial is unknown.

The long-term fate of mRNA within cells is currently unknown.

The mRNA and adenovectorDNA vaccines act as 'synthetic viruses'.

In the young and healthy, and even in many older individuals with vulnerable comorbidities, the encoding-based COVID-19 vaccines will likely transfect a far more diverse set of tissues than infection by the virus itself.

Evidence suggests reverse transcription of mRNA into a DNA copy is possible. This further suggests the possibility of intergenerational transmission if germline cells incorporate the DNA copy into the host genome.

Production of foreign proteins such as spike protein on cell surfaces can induce autoimmune responses and tissue damage. This has profoundly negative implications for any future mRNA-based drug or vaccine.

The spike protein exerts its pathophysiological effects ('spikeopathy') via several mechanisms that lead to inflammation, thrombogenesis, and endotheliitis-related tissue damage and prion-related dysregulation.

Interaction of the vaccine-encoded spike protein with ACE-2, P53 and BRCA1 suggests a wide range of possible biological interference with oncological potential.

Adverse event data from official pharmacovigilance databases, an FDA-Pfizer report obtained via FOI, show high rates and multiple organ systems affected: primarily neurological, cardiovascular, and reproductive.

Pfizer and Moderna mRNA COVID-19 vaccines' clinical trial data independently interpreted has been peer-review and published to show an unfavourable risk/benefit, especially in the non-elderly. The risks for children clearly outweigh the benefits.

Repeated COVID-19 vaccine booster doses appear to induce tolerance and may contribute to recurrent COVID-19 infection and 'long COVID'.

The SARS-CoV-2 pandemic has revealed deficiencies in public health and medicines regulatory agencies.

A root cause analysis is needed for what now appears a rushed response to an alarming infectious disease pandemic.

Treatment modalities for 'spikeopathy'-related pathology in many organ systems, require urgent research and provision to millions of sufferers of long-term COVID-19 vaccine injuries.

5. Structure of SARS-CoV-2 Spike Protein

Cryo-EM electron microscopy revealed the structure of the spike protein at the outset of the pandemic [ 26]. The SARS-CoV-2 spike proteins protrude outwards from the cell wall of the virus and are in red in the schematic diagram in Figure 3 from Cuffari [ 27].

Figure 3.

Diagram of various proteins of SARS-CoV-2 virus. Reprinted from News-Medical.net (accessed on 26 April 2023) Cuffari (2021): What are spike proteins? ( with permission, license from Shuttercock). [ 27].

In the context of SARS-CoV-2 infection, the spike protein is a pathogenic determinant of cell invasion, consisting of two subunits: S1 at the distal end of the spike glycoprotein pointing outwards from the virus constructed of an N-terminal domain (NTD) and a trimer of three receptor binding domains (RBD), and S2 consisting primarily of a C-terminal region that forms the stalk of the spike protein and embeds proximally to the virus' envelope or membrane.

The virus uses the spike protein to bind with ACE-2 receptors on cell surfaces to enter the cells. For this to happen, the receptor binding domain (RBD) on the S1 subunit undergoes hinge-like extension from the 'down' to 'up' position to interact with the ACE-2 receptor.

Figure 4, from Wrapp et al. [ 26], shows one of the three 'trimer' RBDs in green in the 'up' position while the other two RBDs are 'down' and inaccessible to the attachment to ACE-2. The diagram on the left is the view of the spike protein in profile and on the right is a view of the S1 subunit or top of the trimeric spike protein from above.

Figure 4.

Structure of 2019-nCoV S in the prefusion conformation. ( A) Schematic of 2019-nCoV S primary structure coloured by domain. Domains that were excluded from the ectodomain expression construct or could not be visualised in the final map are coloured white. SS, signal sequence; S2′, S2′ protease cleavage site; FP, fusion peptide; HR1, heptad repeat 1; CH, central helix; CD, connector domain; HR2, heptad repeat 2; TM, transmembrane domain; CT, cytoplasmic tail. Arrows denote protease cleavage sites. ( B) Side and top views of the prefusion structure of the 2019-nCoV S protein with a single RBD in the up conformation. The two RBD down protomers are shown as cryo-EM density in either white or gray and the RBD up protomer is shown in ribbons coloured corresponding to the schematic in ( A). Reprinted from [ 26] Figure 1, Copyright (2022) with permission.

5.1. Does the Vaccine Produced Spike Protein Have Protective Closed RBDs?

The SARS-CoV-2 virion carries spike protein in the form of trimers, predominantly in prefusion form. Prefusion spike protein trimers on each virus are found in various conformations, either closed with all three RBDs lying down at the top of the spike-or open, in which one or more of the RBDs protrude from the top of the spike. The receptor binding site (RBS) is largely inaccessible when the RBDs are in the down position. Spike protein contains a furin cleavage site, where it can be split into S1 and S2 subunits which facilitates infectivity. Serine protease is necessary to split the spike protein into S1 and S2 subunits which greatly increases infectivity via the ACE-2 receptor.

After interaction with the receptor, the spike protein undergoes a conformational rearrangement leading to exposure of the S2 subunit, insertion of the fusion peptide into the membrane of the target cell, and refolding of S2. This refolding pulls the fusion peptide and transmembrane domain of the spike protein together, drawing the target cell and viral membranes together and causing their fusion. As an analogy, imagine a bottle opener pulling the cork up from the bottle neck-but the cork is connected to a cell membrane that gets pulled up along with it [ 28].

The commercially available vaccines in Australia rely on engineered mutations in the spike protein designed to stabilise the prefusion state and reduce the transition into the post-fusion form and therefore limit cleavage. Mutations include the replacement of two residues with a double proline (e.g., Pfizer/BioNTech, Moderna, Novavax, and Janssen), or mutations in the furin cleavage site for protease resistance (Janssen).

Given amassed data that suggest mRNA and adenovectorDNA-created spike proteins cause harm, these theoretical safeguards appear to have failed.

There are several possible reasons for the failure of this system. Since only the mRNA, not the full-length spike protein, gets injected with the lipid-nanoparticles, there is the possibility that the mRNA fragments are not full-length, due to suboptimal synthesis or degradation after manufacture. Spike protein could then be partially expressed as truncated spike protein with a conformation that allows cleavage into a peptide part and a functional S1 or S2 subunit.

Even with full protein code expression, some cleavage can still happen inside cells. No biological system is 100% effective, and the mutation is only supposed to reduce, not completely prevent cleavage into S1 and S2. The transport of spike proteins or subunits via exosomes, direct cell fusion and nanotube tunnels to other cells is still possible. Expression errors inside the cell could lead to spike proteins retaining certain functions. Contamination with replication-capable plasmid vectors leaves the option of mutation during replication or insertion into the genome.

The spike protein is not only toxic through binding of ACE-2 receptors, but it also has cytotoxic effects inside cells through interaction with cancer suppressor genes BRCA and P53 and mitochondrial damage, coagulopathies through direct contact with cellular proteins, and is neurotoxic through accumulation, with spread and reconfiguration of prion proteins into their pathologic form. The accumulation of spike protein inside cells could have toxic and apoptotic effects [ 29].

5.2. Toxin-Like Domain in the RBD

This spike toxin-like binding domain is a part of the RBD, adjacent to the ACE receptor binding site and has been demonstrated both in a computer-simulated study [ 32] and in electrophysiological studies, to bind preferentially to the α7 nAChR in nanomolar doses, similar to neurotoxins, such as bungarotoxin. The active peptide SCoV2P potentiates and inhibits acetylcholine (ACh)-induced α7 nAChR responses by a potential allosteric mechanism in nanomolar potencies and nicotine enhances these effects. At low doses, it potentiates and at higher doses, it inhibits nAChR function [ 33].

This binding model could provide logical explanations for the acute inflammatory disorder and other conditions in patients with COVID-19, long COVID, and vaccination injury, which may be linked to severe dysregulation of the central nervous system.

6. Reasons for Concern: Pharmacodynamic, Pharmacokinetic, and Pathophysiological

Pharmacokinetic and pharmacodynamic data give cause for concern about the conceptual design of the mRNA and adenovectorDNA COVID-19 vaccines and lay the groundwork for understanding the pathophysiology that is now being widely reported. There is uncontrolled biodistribution as well as durability and persistent bioavailability of the spike protein.

6.1. Gene-Based Vaccines Are Novel Experimental Technology

The unprecedented number of adverse events appears to be associated with the spike proteins produced by the gene-based technologies employed by Pfizer, Moderna, AstraZeneca, and Johnson and Johnson. Viral-vectorDNA technology is also employed in the Sputnik V and EpiVacCorona COVID-19 vaccines in Russia, iNCOVACC in India, and Convidecia in China. But the majority of COVID-19 vaccines, mostly made in non-Western countries, are traditional protein-based or inactivated virus non-genetic vaccines [ 34, 35].

The gene-based COVID-19 vaccines fall into a special class of therapeutic agents defined by the FDA as "gene therapy products" [ 36], such that recipient cells produce antigens for transmembrane expression, or to leave the cell, to secondarily invoke an immune response. By design, therefore, by employing virus-like invasion and hijack of cellular transcription, both mRNA and adenovectorDNA gene-based vaccines cause non-immune cells to become de facto antigen-presenting cells, in their mode of immunogenicity. Therefore, these novel vaccine platforms risk tissue damage secondary to cytopathic autoimmune responses, raised against cells expressing foreign spike antigens.

Before the SARS-CoV-2 pandemic, the use of such technology was experimental and mostly restricted to making proteins for the therapy of metastatic cancer. No mRNA vaccines had ever been authorised for public usage prior to the COVID-19 pandemic [ 37] and viral-vectorDNA vaccines only had limited use for Ebola, Dengue, and Japanese encephalitis [ 38].

6.2. Wide Distribution of Lipid-Nanoparticle

Turni and Lefringhausen [ 42], in "COVID-19 vaccines-An Australian Review", note that the lipid-nanoparticle, the carrier for synthetic mRNA, is potentially inflammatory in its own right, crosses membranes and distributes widely in the body. It crosses both the blood-brain barrier and the blood-placenta barrier. They cite the EMA report on the Moderna vaccine "that mRNA could be detected in the brain following intramuscular administration at about 2% of the level found in plasma" (p. 491). They also cite research [ 43, 44, 45] that describes how and why lipid-nanoparticles easily traverse the blood-brain barrier.

Figure 5.

Biodistribution of lipid-nanoparticle in rat, Pfizer study November 2020. From TGA FOI reply 2389-6 [ 5] (p. 45).

Although the highest levels went to the spleen and liver, where high cell turnover helps timely repair of any cytotoxic damage, the lipid-nanoparticle, and by implication the mRNA, went to seemingly all organs, particularly the ovaries and adrenal glands but also the brain, eyes, heart, testes, uterus, pituitary gland, spinal cord, thymus, bone marrow.

The Pfizer rat biodistribution study has been corroborated. Chinese researchers injected mice with lipid-nanoparticle-mRNA complexes (mRNA-LNPs) encoding the firefly luciferase gene and biodistribution from the injection site "became rapidly distributed throughout the body with a large presence in the liver" and the "non-linear relationship between the LNP exposure and the protein expression level varies in different tissues and organs" [ 48] (p. 114). Smaller mRNA-LNP complexes transfected further and relatively smaller amounts of mRNA in the liver and lymph nodes produced higher rates of encoded bioluminescent protein than at the injection site muscle. The authors stated:

6.3. Long-lasting Pseudouridine mRNA

Röltgen et al. [ 53] found persistence for the full 60 days duration of their study of both mRNA and free spike proteins in the cytoplasm and nuclei of germinal cells in axillary lymph nodes ipsilateral to deltoid muscle injection site. Spike protein persisted in 96% of vaccinees blood up to 2 days post-vaccination and was still present in 63% of vaccinees 1 week after the first dose. After the second dose, the detection of spike protein "is impeded ... likely due to ... anti-spike antibodies" (p. 1037). However, as shown earlier the modified RNA molecules are extraordinarily stable, and as long as they persist inside the cell, and the cell is not attacked and killed by the immune system, intracellular ribosomal spike protein production will persist. No studies have determined the stability of the vaccine-induced spike protein, but free spike protein has been found circulating up to 19 days post-vaccination in the plasma of young individuals with post-vaccine myocarditis [ 54].

The findings of these studies are consistent with the 14-day half-life for the mRNA-LNP in the Japanese Ministry of Health Pfizer rat biodistribution study [ 46] and are summarised in Table 1.

Table 1.

Author

Constituents/Tissue Type/Assay Technique

Duration Measured

Animal

Human

Röltgen et al. (2022) [ 53]

mRNA and Spike Protein in ipsilateral lymph nodes;
2-7 days post dose in blood

60 days

Yonker et al. (2023) [ 54]

Spike Protein in blood

1-19 days in cases of myocarditis

Several possible ways for COVID-19 vaccines to perturb the immune system are hypothesised by the authors-via the lipid-nanoparticles, N1-methylpseudouridine in mRNA, the spike protein (particularly the S1 subunit), antibody-dependent enhancement and overwhelming antigenic stimulus [ 58]. Our review of a large and growing literature reveals these concerns to have an evidentiary basis, and there to be a pathogenic role for the spike protein.

6.4. Nanoparticle Toxicology

Wang et al. showed in 2018 that even small amounts of nanoparticles taken up via lungs or skin can lead to cytotoxic effects [ 60]. When ingested, nanoparticles target predominantly the mesenteric lymph nodes, liver, and spleen, while when injected as a drug carrier, they can pass any barrier and translocate to the brain, ovaries, and testis, mainly after phagocytosis by macrophages which help distribute them across the body. Reproductive toxicity effects beyond the scope of this review.

The molecular mechanisms involved in nanoparticle toxicity to the reproductive system are not fully understood, but possible mechanisms include oxidative stress, apoptosis, inflammation, and genotoxicity through induction of reactive oxygen species (ROS), causing damage at the molecular and genetic levels which results in cytotoxicity and DNA damage.

Of particular concern in mRNA-LNP complexes are the two propriety functional excipients, ALC-0315 and ALC-0159, never before used in a medicinal product and not registered in either the European Pharmacopoeia or in the European C&L inventory [ 61]. A question in the European Parliament in December 2021 noted that "Echelon, the manufacturer of these nanoparticles, specifies they are 'for research only and not for human use'". The reply on behalf of the European Commission was that the excipient "in Comirnaty has been demonstrated to be appropriate ... in compliance with the relevant EMA scientific guidelines and standards" [ 62]. Despite this reassurance, the presence of electrolytes in the preparation and manual dilution before inoculation raises serious questions about the stability of the resulting suspension and the polydispersity index of the nanomaterials contained in it, factors that can be hypothesised as the root causes of numerous post-vaccination adverse effects.

A nanoparticle in solution forms a colloidal system whose stability prevents the aggregation of particles through electrostatic repulsion. The parameter used to calculate colloidal stability is the Zeta potential, which refers to the potential generated by a double layer of electric charges. When the potential is low, attractive forces prevail over repulsive and more aggregates will form. The stability of a colloidal biphasic system is a precarious balance dependent upon ratios, processing methods, correct temperatures, and the presence of electrolytes [ 63]. After dilution with sodium chloride solution, the final ratio in Comirnaty is 2.61 mg of electrolytes versus only 0.48 mg of ALC-0315 + ALC-0159. This can only lead to a drastic reduction in the Zeta potential, with predictable aggregation, agglomeration, and, finally, flocculation. One can postulate the damage caused by aggregation of nanoparticles in capillaries throughout the body.

Should the colloidal suspension stay stable enough to disperse in lymph and blood, the nanoparticles as well as their toxic load will distribute across the body, cross blood-brain, blood-placental and other biological barriers and likely cause cell death and inflammation wherever they accumulate. Additionally, the elimination of toxic nanoparticles from the body is not straightforward. Particles of 5.5 nm or less can be excreted after glomerular filtration in the kidneys via the urinary tract. Larger particles could in theory be broken down going through the hepatobiliary tract, however, tend to be bound by, e.g., Kupffer cells, the resident macrophages, which slows down their processing considerably [ 64]. The mRNA-LNP complexes are around 100 nm in size and well above the size which allows their elimination via the kidneys. This would account for their accumulation in the liver and the observed liver toxicity.

6.5. Lipid-Nanoparticles Are Pro-Inflammatory

The lipid-nanoparticles used in the COVID-19 vaccines have been found to induce significant inflammatory cytokine secretion and macrophage inflammatory proteins with cell death [ 43]. Ndeupen et al. [ 43] note this pro-inflammatory effect of the lipid-nanoparticles would increase the vaccine adjuvant immunogenicity of the COVID-19 mRNA vaccines and add to the adverse events. The authors did not consider the widespread biodistribution of the lipid-nanoparticle, and therefore the potential for wide-ranging serious COVID-19 vaccine adverse effects across organs and systems.

Trougakis et al. [ 65] reviewing literature on adverse events from COVID-19 mRNA vaccines, noted the risk of spike protein-driven pathology, which they termed the "spike hypothesis". However, Trougakis and colleagues also reviewed evidence of lipid-nanoparticles' pro-inflammatory properties from animal model studies. These include "activating Toll-like receptors, excessive neutrophil infiltration, activation of diverse inflammatory pathways, and production of various inflammatory cytokines and chemokines" [ 65] (p. 544).

PEG is known to cause anaphylactic reactions in some people, which is stated as a known adverse event in the vaccine patient information leaflet. Beside lipid-nanoparticle-encapsulated mRNA being highly inflammatory, antibodies against the spike protein damage cells and tissue that produce the spike protein. Regardless of which antigen is produced, damage to cells will occur in an autoimmune reaction [ 67].

Mechanisms involved in autoimmune damage to cells producing an endogenous protein include the development of cross-reactivity to the endogenous protein [ 68], immune-mediated toxicity [ 69], and immune tolerance due to switching to IgG4 [ 70]. Switching to an IgG4 immune response has consequences for cancer susceptibility [ 71], pregnancy [ 72] and IgG4-related diseases, which are chronic inflammatory conditions [ 73].

Another risk, and problematic with prior vaccines against coronaviruses both in the human and veterinary field, is the risk of antibody-dependent enhancement [ 66].

6.6. Novavax COVID-19 Vaccine Toxicity and Novel Lipid-Nanoparticle Technology

That lipid-nanoparticle biodistribution makes an important contribution to adverse events is further suggested by adverse event reports from the protein-based Novavax COVID-19 vaccine Nuvaxovid. It has the novel technology of a lipid-nanoparticle matrix which could potentially increase biodistribution of the unmodified spike protein, with intact furin cleavage and receptor binding domain sites. In response to a query about biodistribution studies, Novavax replied in mid-2021 that "a pharmacokinetic/pharmacodynamic study has not been performed on the Novavax COVID-19 vaccine" (personal communication Novavax-Parry, 30 July 2021).

Myocarditis adverse events have been reported for the Novavax COVID-19 vaccine in several nations including New Zealand, where the regulator has released an "Alert Communication" on myocarditis [ 74]. This suggests a pathogenic amount of spike proteins from the Novavax COVID-19 vaccine can on occasion reach the heart. Overall, the adverse event reports from the Novavax COVID-19 vaccine are less than from the gene-based vaccines, which would be consistent with a dose-response effect for spike proteins. However, the lipid-nanoparticle matrix itself may be responsible for some of the myocarditis reports.

6.7. AstraZeneca COVID-19 Vaccine Biodistribution Data

In October 2022 a FOI request (MHRA IR07151D) obtained AstraZeneca documents that had been submitted to the British MHRA. According to the AstraZeneca "Nonclinical Overview" dated 21 December 2020, the rationale for initially not performing biodistribution studies on the AstraZeneca adenovirusDNA COVID-19 vaccine was that prior studies on viral vector vaccines showed minimal spread from the deltoid muscle and axillary lymph nodes to distal organs [ 75]:

However, a later AstraZeneca "Nonclinical Overview" dated 26 April 2021, which included new mouse biodistribution studies on the company's COVID-19 vaccine did reveal biodistribution to distal organs [ 6]:

" The highest levels of AZD1222 vector DNA (103 to 107 copies/µg DNA) were observed in the intramuscular administration sites and sciatic nerve (close proximity to the administration sites) on Day 2. Lower levels of AZD1222 vector DNA (<LLOQ to 10⁴ copies/μg DNA) were observed in the bone marrow, liver, spleen and lung on Day 2. The levels of AZD1222 and the number of tissues with detectable levels of AZD1222 vector DNA decreased from Day 2 to 29, indicating elimination ".

[ 6] (p. 14)

The document stressed that the viral-vector itself was not replicating as an adenovirus, but that misses the point of protein production of a toxic foreign antigen in bodily organs. Although this suggests lesser quantities of the viral-vectorDNA COVID-19 vaccines are widely biodistributed than with the lipid-nanoparticle carried modified mRNA COVID-19 vaccines, the capacity of the adenovectorDNA vaccines to produce significant quantities of spike proteins remains. An autopsy series of three cases of vaccine-induced immune thrombotic thrombocytopenia (VITT) with cerebral thrombosis related to the AstraZeneca COVID-19 vaccine found spike proteins in thrombosis and cerebral vein walls [ 7]. The authors state in the abstract:

" SARS-CoV-2 spike protein was detected within the thrombus and in the adjacent vessel wall. Data indicate that neutrophils and complement activation associated with antispike immunity triggered by the vaccine are probably involved in the disease process."

6.8. Traditional COVID-19 Vaccines Not Contributing High Adverse Event Reports

Traditional COVID-19 vaccines have not produced the high rates of adverse event reports that characterise the gene-based COVID-19 vaccines. This is further evidence that the risk is in the body-wide biodistribution and prolonged production of spike proteins. It points to pathogenicity of the spike protein and, given the evidence described above, also the lipid-nanoparticle carrier matrix.

6.9. Autoimmune Risk of Foreign Antigens Presented by the Body's Own Cells

As described above, evidence shows the spike protein to be innately toxic. Even if it were non-toxic in its own right, by virtue of its foreignness, spike protein could still produce pathophysiological damage through autoimmune responses. A straightforward consequence of a foreign protein. The lipid-nanoparticle matrix permits widespread biodistribution of mRNA gene codes to cells in most or all organs. The subsequent expression of the spike protein on cell surfaces, and as a soluble protein within the organs and blood stream, induces T-cell destruction of cells and tissues and B-cell antibodies. The latter may also cause immune complex deposition further damaging tissues via type III hypersensitivity.

Tissue damage, therefore, can be caused by the spike protein via autoimmune reactions, even if it is 'non-toxic'. While this is of minor consequence in a muscle such as the deltoid, it causes serious and fatal adverse events when occurring in critical organs such as the brain, ovaries, and heart. The method of delivery-mRNA gene therapy via lipid-nanoparticles that traverse biological membranes-is a core problem and a key reason why this technology has never been commercially marketed, until now.

The fact Moderna and other big pharmaceutical companies plan large-scale mRNA vaccine manufacture for many other diseases, in the absence of a full and detailed inquiry, is, therefore, deeply troubling.

6.10. Pathophysiology of Virus and Vaccine Spike Protein

The natural course of new pandemic/epidemic viruses is to become more infectious and less pathogenic with time. This has demonstrably been the case with SARS-CoV-2 where the original Wuhan strain and subsequent alpha and other early variants were quite pathogenic, the delta variant spread more easily but was somewhat less pathogenic, and the various omicron subvariants have been highly infectious but even less pathogenic in illness severity. In particular, the omicron subvariants have targeted the upper respiratory tract rather than the lower respiratory tract, leading to less systemic penetration of the virus and the spike protein [ 83].

On the other hand, the mRNA and adenovectorDNA vaccines cause human cells to manufacture a slightly modified version of the original Wuhan strain spike protein. Some "bivalent" booster doses add genetic code for omicron variant spike protein [ 84, 85]. If an individual suffers wide biodistribution of this genetic code, many more spike proteins can be produced systemically than generally occurs with the natural virus. This is more likely for anyone who is young and healthy. The elderly and those with comorbidities have a greater risk of serious SARS-CoV-2 viral infection deep in the lungs and systemically, whereas the young and healthy tend to rid themselves of the virus in the upper respiratory mucosa. Therefore, in the young and healthy the encoding-based COVID-19 vaccines will transfect a far more diverse set of tissues than infection by the virus itself.

Many studies have demonstrated the spike protein is toxic. In "Understanding the Pharmacology of COVID-19 mRNA Vaccines: Playing Dice with the Spike?", Cosentino and Marino (2022) reviewed the evidence for the toxicity of the spike protein [ 86]. They argued that the COVID-19 mRNA vaccines should rightly be described as "prodrugs" as they meet the dictionary definition: "a pharmacologically inactive substance that is converted in the body (as by enzymatic action) into a pharmacologically active drug". This occurs via the mRNA action in ribosomes to cause the synthesis of the spike protein [ 86] (p. 3).

Cosentino and Marino (2022) reviewed the evidence for widespread biodistribution of the mRNA and concluded that "evidence strongly supports the possible link between inappropriate expression of S protein in sensitive tissues and subsequent tissue damage" [ 86] (p. 2).

They reviewed the literature on the pharmacology and pathophysiological effects of the spike protein on bodily tissues, which include [ 86] (p. 4-5):

Binding to ACE-2 receptors as a "potential trigger for platelet aggregation, thrombosis and inflammation, as well as for hypertension and other cardiovascular disease".

Disruption of CD147 transmembrane glycoprotein which interferes with cardiac pericyte and erythrocyte function may result in myocarditis, haemolytic anaemia, blood hyperviscosity, and possibly neurodegenerative processes.

Binding to Toll-like receptors 2 and 4 (TLR2, TLR4), with theoretical pathogenic effects via increased inflammatory cytokine cascades, due to (1) activation of Nuclear Factor kappa B (NF-κB pathway) and deficient macrophage immune function via TLR2, and (2) lung damage, myocarditis and multiorgan injury via TLR4, that had yet to be properly investigated by the world's research community.

Binding to the high affinity oestrogen receptor alpha (ER alpha) is possibly responsible for the menstrual irregularities commonly observed after COVID-19 vaccination and raising concerns of potential involvement in breast cancer.

Spike protein S2 subunit specifically interacts with proteins p53 BP1 and BRCA1. The p53 BP1 is a well-established tumour suppressor; the BRCA1 is frequently mutated both in breast cancer and in prostate cancer [ 87].

Cosentino and Marino noted that these "potential toxicological issues" were not "taken into consideration in the studies that led to the marketing authorisation, precisely because ... these products were treated as conventional vaccines", when in fact they are gene insertions acting as prodrugs [ 86] (p. 5).

In vitro research found the receptor binding domain (RBD) of the spike protein (the S1 unit) was the most active agent to trigger a pro-inflammatory response from dendritic cells [ 88].

Further in vitro research with human pulmonary artery muscle and endothelial cells treated with full-length spike protein or the RBD alone, found in this case the RBD to be relatively inert, but the full-length spike protein to induce enlargement of the pulmonary vessel cells via phosphorylation of protein MEK (mitogen-activated protein kinase kinase) [ 89]. This was found to also be the case in vivo when intratracheal administration of the S1 unit/RBD into transgenic mice with human ACE-2 on their cells showed a dramatic increase in inflammatory cytokines in bronchial lavage fluid from mice who received the spike protein S1 unit, whereas this was minimal for control mice (intratracheal saline) and mild and late for whole spike protein administered mice, indicating the cleaving of the S1 (RBD) unit increases the ACE-2 associated pathology [ 90].

In a preprint, McKernan et al. [ 91] quantify the pharmacokinetics of the mRNA vaccines as creating greater numbers of spike proteins than the SARS-CoV-2 virus, and more systemically in most people not prone to overwhelming COVID-19 viral infection:

Human tissue production of antigens means that the dose is likely to vary between individuals. This will be for reasons of individual genetics and physiology, the tissues exposed to the code, batch and vial variability of the product and manner of transportation, refrigeration, and administration. In terms of the toxicological principle dosis sola facit venenum (the dose makes the poison), this aspect on its own casts doubt on the safety of mRNA and viral vector DNA vaccines.

Around the time the COVID-19 vaccines were released to the public, researchers at the Salk Institute found that the SARS-CoV-2 virus relies upon the spike protein binding to ACE-2 receptors on host cells to gain cell entry [ 92]. ACE-2 is protective in the cardiovascular system, and SARS-CoV-2 spike protein promotes lung injury through a decrease in the level of ACE-2. The Salk Institute team showed that the spike protein alone can damage vascular endothelial cells by downregulation of ACE-2, inhibition of endothelial nitric oxide synthase (eNOS), impairment of mitochondrial function and direct impairment of endothelial function.

6.11. Disruption of the Nicotinic Cholinergic Anti-Inflammatory Pathway

High doses of the toxin-like spike protein binding domain (RBD) inhibit acetylcholine (ACh)-induced α7 nAChR responses. Inhibition of these α7 nACHRs has profound effects [ 33]. The nicotinic cholinergic system has been labelled the 'Cholinergic Anti-inflammatory Pathway' (CAP), as the activation of these receptors controls inflammation and their inhibition results in uncontrolled inflammation. The CAP forms a multi-faceted network, with distribution in neuronal and non-neuronal cells, and diverse functions throughout the body. In addition to the nervous system, α7 nAChRs are expressed in non-neuronal cells such as lymphocytes, monocytes, macrophages, dendritic cells, adipocytes, keratinocytes, endothelial cells, and epithelial cells of the intestine and lung. With such widespread distribution, nAChRs could be implicated in the pathophysiology of severe COVID-19 via mechanisms, both through and independent of the cholinergic anti-inflammatory pathway [ 32].

The modulation of inflammatory and immune response by the CNS through the vagus nerve is based on bi-directional communication between the immune and nervous systems. Afferent vagus nerve fibres, located in nucleus tractus solitarius, provide sensory input to the CNS about the inflammatory status that can result in the transmission of efferent signals, originating from the dorsal motor nucleus, to control the inflammatory response. Such a response is rapid and localised, unlike the diffusible anti-inflammatory network, which is slow, distributed, non-integrated and dependent on concentration gradients [ 32].

Activated via the vagal nerve release of ACh, nACHRs are found in the immune system on T-cells, B-cells, macrophages, monocytes, neutrophils and mast cells and act to reduce inflammation, including the reduction of proinflammatory cytokines, such as IL-6, while promoting anti-inflammatory cytokines such as IL-4 [ 93]. Dysregulation of nAChR by SARS-CoV-2 could also suppress the counterbalance to the sympathetic nervous system and thus promote the central sympathetic drive and the development of the sympathetic-driven cytokine storm [ 94]. In turn, the sympathetic storm triggers oxidative stress and hyperinflammation by increasing the generation of reactive oxygen species (ROS) and the release of pro-inflammatory cytokines.

NAChR are also found in the respiratory tract. Subtype α3β4 nAChR support cilia function and mucociliary clearance, and α7 nAChR stimulation is anti-inflammatory. Hence, the inhibition of both these receptor types, as spike protein is able to do, would contribute significantly to the lung pathology seen in both acute COVID-19 and long COVID [ 95].

SARS-CoV-2 infection-induced stress and suppression of the cholinergic pathways via nAChR inhibition may also activate the sympathetic nervous system (SNS) leading to neuro-hormonal stimulation and activation of pro-inflammatory cytokines with further development of a sympathetic storm. Sympathetic over-activation in COVID-19 is correlated with an increase in capillary pulmonary leakage, alveolar damage, and the development of acute respiratory distress syndrome. Furthermore, SARS-CoV-2 can spread through pulmonary mechanoreceptors and chemoreceptors to the medullary respiratory centre in a retrograde manner resulting in sudden respiratory failure as a result of nAChR inhibition in the parasympathetic medullary centres [ 96].

Once someone is infected with SARS-CoV-2, the immune system is mobilised. As the virus replicates, cell and viral debris or virions may interact with the nAChRs to block the cholinergic anti-inflammatory pathway. If the initial immune response is not enough to combat the viral invasion at an early stage, the extensive and prolonged replication of the virus will eventually disrupt the cholinergic anti-inflammatory pathway and seriously compromise the ability to control and regulate the immune response. The uncontrolled action of pro-inflammatory cytokines will result in the development of cytokine storm, with acute lung injury and acute respiratory distress syndrome (ARDS), coagulation disturbances and multiorgan failure. Based on this hypothesis, COVID-19 appears to eventually become a disease of the nicotinic cholinergic system [ 92].

This same mechanism can explain both the breadth and severity of symptoms experienced in long COVID and in COVID-19 vaccine injuries. The former shows failure to clear spike protein and virus, with uncontrolled immune activation and sequelae [ 97], and in the latter vaccine injuries, where spike protein overwhelms the system and is produced for months, there is increased load with each subsequent injection. This also provides a mechanism for possible interventions with α7 nAChR agonists and positive allosteric modulators (PAMS).

7. Evidence of 'Spikeopathy'-Spike Protein Pathogenicity

The spike protein of SARS-CoV-2 has turned out to be pathogenic. The term "spikopathy" has been coined [ 98] as its pathological effects, like tuberculosis, appear to be legion, widespread in body organs, and induce a myriad of known diseases and syndromes. The term is spelled "spikeopathy" by others on the internet and we have chosen that spelling.

Figure 6 shows the FDA was aware of this potential before the public release of the gene-based COVID-19 vaccines. It is the 16th slide from a PowerPoint presentation of the "Vaccines and Related Biological Products Advisory Committee (VRBPAC) 22 October 2020, Meeting" [ 99]. What is striking is the predictive accuracy of these mostly neurological, cardiovascular, and autoimmune "possible adverse events" with those reported to VAERS and other global vaccine injury databases.

Figure 6.

Slide 16 FDA's VRBPAC meeting, Oct. 2022 [ 99].

The website www.react19.org lists as of June 2023 over 3400 published papers and case reports of COVID-19 vaccine harms under over twenty organ system and syndrome headings [ 100]. Here, we will review some key organ systems in relation to the pathogenic effects of the COVID-19 mRNA and adenovectorDNA-produced spike proteins.

7.1. Cardiovascular Pathogenesis

Literature accumulates about the cardiovascular harms of COVID-19 vaccines. For example, as of June 2023 react19.org, under the heading "Cardiac", lists 432 peer-reviewed papers and case reports covering myocarditis, cardiomyopathy, myocardial infarction, hypertension, aortic dissection, postural orthostatic tachycardia syndrome (POTS), tachycardia, and conduction disturbance [ 100].

7.1.1. Myocarditis and Pericarditis

Reports of myocarditis and pericarditis are particularly numerous. Yonker et al. [ 54] found free spike proteins in the blood of 16 adolescents and young adults who developed post-vaccination myocarditis, but not in 45 post-vaccination age-matched controls without myocarditis. The authors examined immuno-profiles and free spike protein plasma concentrations in young subjects with myocarditis after vaccination with COVID-19 mRNA vaccines. Significantly elevated full-length free spike protein concentrations, unbound to antibodies, were found in the myocarditis patients compared with controls. Antibody profiles and T-cell responses were similar between subjects with myocarditis and carefully age-matched controls, but it may be reasoned that part of the variance seen with regard to myocarditis as a complication of mRNA vaccination, may be explained by the fact that some achieve greater transcription and secretion into the blood. This raises serious concern about the pathogenicity of free spike protein in such cases of myocarditis.

Avolio et al. [ 101] found the free SARS-CoV-2 spike protein, separated from the virus, could cause microvascular disease via several mechanisms, which include stimulation of cardiac pericytes to engage in pro-inflammatory cytokine production via CD147 receptor binding. Further evidence for the pathogenicity of spike protein is from mouse studies where spike protein-induced cardiac fibrosis and myocardial contractile impairment may underlie COVID-19-related cardiomyopathy [ 102].

The possibility that COVID-19 vaccine-associated myocarditis, as opposed to the hypersensitivity myocarditis seen with agents such as the smallpox vaccine, is in fact autoimmune, is considered by Baumeier and colleagues [ 103] in a series describing 15 cases with endomyocardial biopsies (EMB), a study is discussed in a later section of this paper. Like other studies and case reports, lymphocytic infiltration was seen in association with intracardiac spike expression (although the authors did not specifically refer to lipid-nanoparticle biodistribution characteristics).

From the above, although much laboratory study remains to be conducted regarding the myocardial inflammation seen prominently after mRNA vaccinations, it appears that spike protein plays a role. Whilst molecular mimicry is not the reason, direct toxic effects of spike protein may be implicated, in addition to the reaction of the immune system to the presence of spike protein, either expressed in or deposited in the myocardium. That myocarditis is precipitated by spikeopathy is further indicated in that the adenovectorDNA COVID-19 vaccines of both AstraZeneca and Johnson & Johnson, as well as the Novavax protein-based lipid-nanoparticle embedded vaccine, have been reported as causative [ 105, 106].

How common is COVID-19 vaccine-induced myocarditis and pericarditis? As a baseline, a study published on 7 January 2020, the eve of the SARS-CoV-2 pandemic, reported: "viral myocarditis has an incidence rate of 10 to 22 per 100,000 individuals [ 107].

As to community epidemiological incidence, a review in the New England Journal of Medicine [ 108] noted that the annual incidence rate depended on the level of investigation:

Health authorities like the FDA, TGA and other regulators have claimed that post-COVID-19 vaccination myocarditis is very rare. An early study of 2.39 million Kaiser Permanente insured Californian adults who received at least one dose of a Pfizer or Moderna COVID-19 vaccine found only 15 cases of post-vaccine myocarditis, all males with a mean age of 25 years [ 109]. However, cases were based on physician reports to the Kaiser Permanente immunisation committee or hospitalised cases within 10 days of vaccination. Milder cases could have been missed; physicians might not always have reported cases to the committee.

A systematic review of pharmacovigilance reports to US VAERS, UK Yellow Card, and EU EudraVigilance databases up to March 16, 2022, found 18,204 submitted events of myocarditis and/or pericarditis, some fatal [ 110]. Given hundreds of millions of vaccine recipients, the authors noted this to be a rare event.

The FDA recognised the risk for myocarditis and pericarditis from the COVID-19 mRNA vaccines was real, especially in younger males after the second dose, but judged it to still be rare, and cited a VAERS-derived figure of 6.5 per 100,000 and up to 20 per 100,000 for adolescent boys [ 111]. The FDA did not calculate that pharmacovigilance databases, like its own FAERS (FDA Adverse Event Report System) and the CDC's VAERS, have a large under-reporting factor.

A common factor in this pharmacovigilance-derived estimate of the FDA, as well as those of others, is the failure to mention the perennial problem of underreporting in passive notification systems. Pharmacovigilance databases, like its own FAERS and the CDC's VAERS, are acknowledged to have large under-reporting factors. As to how large the under-reporting factor is, is a matter of debate.

Compounding the phenomenon of underreporting in the case of myocarditis, is that this diagnosis is difficult to make, and often depends on the availability of specialty units, cardiac MRI facilities and/or endomyocardial biopsy (EMB). The diagnosis can mimic myocardial infarction and thus can be misdiagnosed. In this regard, the paper by Baumeier et al. [ 103] (discussed later in this paper), noted that a third of those with histologically confirmed myocarditis, categorised as vaccine-associated on the basis of history and exclusion of other causative agents, did not have cardiac MRI evidence of myocarditis. Further, many cases of myocarditis are subclinical and may be missed in the acute phase. This does not mean, however, that a benign course is always expected since even minor fibrosis and scarring of the myocardium can create arrhythmogenic foci and may present later with serious and fatal arrhythmias, or else may eventually lead to heart failure (so-called inflammatory cardiomyopathy) [ 112]. Hence, it is rational to say that the exact frequency of vaccine-associated myocarditis is unknown: cases can be subclinical, missed, or misclassified and even specialised imaging may underdiagnose.

An indication of how common subclinical myocarditis, or at least myocardial involvement, might be comes from a prospective study in Thailand. Adolescents ( n = 301) with no cardiac history had cardiac biomarkers (troponin-T, creatinine kinase-band (CK-MB)), ECG, echocardiography, and diary of cardiac symptoms at baseline and on days 3, 7 and 14 after the second dose of Pfizer mRNA COVID-19 vaccine [ 113]. Although there was no control group, the diary, physical examination, and ECG results are of concern: "tachycardia (7.64%), shortness of breath (6.64%), palpitation (4.32%), and hypertension (3.99%)" (p. 4). Fifty-four adolescents (18%) had abnormal ECGs. Troponin elevation occurred in five adolescents, echocardiography detected pericardial effusions in three adolescents, and signs of myopericarditis in one adolescent led to ICU admission. In total seven adolescents presented "with myopericarditis, subclinical myocarditis, and pericarditis after second dose vaccination" but apart from the adolescent hospitalised to intensive care, the other six cases were subclinical or mild and easily missed if it were not for this rigorous prospective study [ 113] (p. 8, Table 3).

Although the public health authorities' narrative is that myocarditis from COVID-19 vaccines is mild and self-limiting, the evidence is that symptomatically while this might be the case, pathological changes in these young hearts are persistent. An Italian study followed 13 cases of post mRNA vaccine-induced myopericarditis, myocarditis or pericarditis, median age 15 years, for 12 weeks. Although overt symptoms in all but one case resolved, 12 of the 13 adolescents still had pericardial effusion and six of nine who had cardiac MRI scans had signs of "persistent, although decreased, myocardial injury" at the study end [ 115].

7.1.2. Thrombotic Effects of Spike Proteins

The authors describe the mechanisms by which these clotting effects are more common in younger patients. Angiotensinases prolyl oligopeptidase (POP) and prolyl carboxypeptidases (PRCP) become deficient in older people with cardiovascular diseases and paradoxically this translates to less susceptibility to spike protein-induced cardiovascular pathogenesis, whereas with younger people the risk is increased:

They also propose that pre-existing immunity from SARS-CoV-2 infection or prior vaccination induces greater immune responses to spike protein production by cells, such as platelets, endothelial vascular cells or myocytes, leading to increased inflammation and thrombogenic activity. In Angeli et al. [ 119] they conclude:

Whereas Phase III vaccine trials generally excluded participants with previous immunisation, vaccination of huge populations in real life will inevitably include individuals with preexisting immunity. This might lead to excessively enhanced inflammatory and thrombotic reactions in occasional subjects. Further research is urgently needed in this area.

Live electron microscopy has shown free spike proteins trigger platelets to deform and coagulate via filopodia induction and the interaction of spike protein with platelet integrins to cause coagulopathy [ 121]. Early in the pandemic, mice transfused with transgenic human ACE-2 receptor platelets developed thrombi due to spike protein binding with the ACE-2 receptors on the platelets [ 1]. The authors noted:

The spike protein also was found to "competitively inhibit the bindings of antithrombin and heparin cofactor II to heparin/HS, causing abnormal increase in thrombin activity" [ 122]. In another mouse study, the spike protein was also found to "bind to the blood coagulation factor fibrinogen and induces structurally abnormal blood clots with heightened proinflammatory activity" and that "spike delays fibrinolysis" [ 123] (preprint).

French researchers at the Méditerranée Infection Institute in Marseille examined the effects of the spike proteins of the SARS-CoV-2 Wuhan, alpha, delta and omicron BA.1 variant on red blood cells (erythrocytes) in vitro and found the spike protein induced haemagglutination (clumping) of erythrocytes, the omicron BA.1 variant achieving this at lower concentrations down to 0.13 ng/µL, the earlier variants down to a concentration of 0.13 ng/µL. The mechanism of action was deduced via molecular modelling to be the positive charge on the spike protein reducing the natural electrostatic repulsion of negatively charged erythrocytes. Interestingly ivermectin when added to the in vitro solution bound strongly to the spike protein and prevented or reversed the haemagglutination depending on whether added pre or post the spike protein. The authors note the implications for treatment of vaccine adverse effects [ 124].

The plasma and internal membranes of other eukaryotic cells can be considered to function with anions and cations acting as a current loop to drive membrane potential on either side of the cell membrane [ 125, 126]. The red blood cell's unique design is a toroid where currents also flow on the surface of the torus. If this static flow on the erythrocyte membrane surface is interrupted by a lack of separation between the negative surface membrane charge and the Stern layer, the zeta potential weakening leads to distortion of shape, decreased electric permittivity, increased viscosity, flocculation and rheological alterations [ 127]. When this surface current flow is static, with efficient separation of the positively charged Stern layer and negative surface membrane charges, the zeta potential is enhanced and the size, shape, proportion, and curvature of the erythrocyte transforms to the optimal shape. Erythrocytes must maintain a biconcave discoid shape in order to efficiently deliver oxygen (O ₂) molecules and to uptake carbon dioxide (CO ₂) molecules [ 128]. The interpolation of a positive spike protein into the negatively charged erythrocyte membrane can thus be expected to result in significant alterations in erythrocyte shape and function.

Thrombotic complications of COVID-19 vaccination involve many potential mechanisms, such as endothelial cell damage, immune response, dysregulation of the renin-angiotensin-aldosterone system, and thrombo-inflammation. Additionally, platelets contain acetylcholine and express α7nAchR. Acetylcholine acts as an endogenous inhibitor of platelet aggregation. Hematopoietic α7nAchR deficiency increases platelet activation and, in experimental studies, α7nAchR stimulation can diminish the pro-inflammatory state and modulate platelet reactiveness via increased levels of nitric oxide (NO). Inhibition of platelet nAChR by SARS-CoV-2 thus promotes platelet hyperreactivity and thrombosis which are hallmarks of COVID-19 and vaccine injury [ 129].

These mechanisms would explain clotting to both the virus and the spike proteins produced by the gene-based COVID-19 vaccines. It also suggests that public health policies that negated natural immunity and mandated COVID-19 vaccination, and booster programs, put the young and non-elderly population at greater risk. To illustrate these increased risks of harms, blindness cases have been reported to pharmacovigilance databases and a recent large study of retinal vascular occlusion diagnoses in the United States from January 1, 2020, to December 31, 2022, found COVID-19 vaccinated individuals with Moderna, Pfizer or AstraZeneca COVID-19 vaccines had a 2.19 hazard ratio increased risk compared with unvaccinated Americans [ 130].

7.1.3. Vaccine-Induced Immune Thrombotic Thrombocytopenia (VITT)

In contrast to the spike protein's role in myopericarditis and thrombogenesis as described above, the syndrome of vaccine-induced immune thrombotic thrombocytopenia (VITT) seen with the adenovectorDNA vaccines of AstraZeneca and Johnson & Johnson, as well as the adenovectorDNA Russian Sputnik V vaccine [ 131], is a rare condition mediated by anti-PF4 platelet antibodies. It appears unrelated to the spike protein, and other components of the adenovectorDNA technology are being investigated [ 132]. It is odd that these vaccines have been mostly withdrawn from markets, whereas the mRNA COVID-19 vaccines with similar issues, albeit by different pathophysiological mechanisms, have not.

7.2. Autoimmune Disease

In 2020, prior to the launch of the vaccines, Lyons-Weiler suggested that more than one-third of COVID-19 proteins, the spike protein included, show problematic homology with key proteins in the human immune system. Thus, there is potential for autoimmune reactions against these proteins [ 8]. Vojdani et al. [ 9] cited Lyons-Weiler and went further in their testing, performing epitope mapping and applied monoclonal anti-SARS-CoV-2 spike protein and nucleoprotein antibodies to 55 human tissue antigens in vitro. They discovered that SARS-CoV-2 antibodies reacted with 28 of the tissue antigens, thus likely playing "a role in the multi-system disease process of COVID-19" (abstract) and may precipitate or exacerbate autoimmune diseases. Their paper was submitted in October 2020 and they noted historical precedents for vaccines causing autoimmune-related disorders and expressed concern that "an insufficiently vetted vaccine might mean trading freedom from COVID-19 to an autoimmune assault in the future" (p. 2).

Vojdani and colleagues found the 28 antigens had molecular mimicry/shared homology and reactivity with:

Khavinson et al. in a paper titled "Homology between SARS-CoV-2 and human proteins" found more than two dozen heptamers and octamers, homologous with human proteins, some of which fuse to extended lengths along the length of the SARS-CoV-2 spike protein [ 136]. They noted that given the "structural similarity, a part of the immune response will be directed against the proteins of the host organism" (p.1).

Kelleni reports on the potential risk of vaccines to induce autoimmune diseases such as thrombocytopenia, myocarditis and immune-induced thrombosis and thromboembolism, all potentially fatal and possible causes of sudden death [ 137].

Most recently, a group from Saudi Arabia has found clear clinical emergence of autoimmune disease after COVID-19 vaccination. A series of exclusively new-onset autoimmune diseases are described after COVID-19 vaccination. The average time between vaccination and new onset disease was 7 days. Cases included vasculitis, neurological disease, systemic lupus erythematosus, inflammatory arthritis, and a case of Sjogren's syndrome [ 138]. A systematic review by Rodríguez et al. documented 928 cases from 464 published reports of new or relapses of autoimmune disease following COVID-19 vaccination [ 139]. The authors noted:

A 23-year-old woman suffered an ocular autoimmune reaction in the form of granulomatous anterior uveitis following her third Pfizer COVID-19 vaccine 15 days earlier [ 146]. The authors commented:

" Autoimmune reaction in the uveal tissue via molecular mimicry as a result of an adaptive humoral and poly-specific cellular immune response against epitopes may be the potential mechanism for post-vaccine uveitis in this patient ".

(p. 1034)

A case report of hepatitis-associated aplastic anaemia (HAAA) following COVID-19 vaccination in a 15-year-old girl from Japan [ 147] cited Talotta [ 148] and postulated:

Repeated antigenic stimulation of immunity, as occurs with the gene-based COVID-19 vaccines' prolonged production of spike proteins, repeated booster doses and recurrent SARS-CoV-2 infections, has seen a rise in IgG4 levels over 480-fold above normal levels [ 149, 150]. This IgG class shift can be associated with serious disease pathology relating to sudden cardiac death [ 151, 152].

It has also been associated with Mikulicz syndrome with systemic involvement, pancreato-hepatobiliary disease, head/neck disease, retroperitoneal fibrosis/aortitis [ 153, 154, 155, 156], as well as lymphadenopathy, sialadenitis, dacryoadenitis, autoimmune pancreatitis, periaortitis/retroperitoneal fibrosis, prostatitis, sclerosing cholangitis, sinusitis, inflammatory pseudotumour, mediastinal fibrosis, skin involvement, sclerosing thyroiditis, hypophysitis, orchitis and colitis [ 157, 158, 159, 160].

These widespread autoimmune and pro-inflammatory effects of spike protein and potentially lipid-nanoparticles illustrate 'spikeopathy' to be another 'great mimicker' akin to tuberculosis, which makes the diagnosis of the underlying aetiology difficult [ 161].

7.3. Neurological Disorders

7.3.1. Neurovascular and Neuroimmunological Aspects

To some degree, the pathophysiology is likely to be via vascular and autoimmune pathology in the central and peripheral nervous system. The spike protein has been found in in vitro human cell cultures to dysregulate brain vascular pericytes by increasing ACE-2 expression leading to these cells lining the cerebral vasculature and adopting a "contractile and myofibogenic phenotype" as well as a "potent inflammatory response" worsened by hypoxia [ 169].

In further mouse experiments infusion of spike protein into brains led to TLR4-mediated neuroinflammation and hippocampal microgliosis with associated memory dysfunction. It was noted in humans that cognitive dysfunction post-COVID-19 was more likely with a particular TLR4 genotype [ 170]. This replicated similar mouse experimentation finding that infusion of the S1 subunit (RBD) to mice hippocampus induced cell death and glial activation and the mice exhibited cognitive deficits and anxiety-like behaviour [ 171].

Tillman et al., (2023) [ 172] described how the co-expression of the S1 and S2 subunits of the SARS-CoV-2 spike protein, via a helical motif in the spike neck, causes profound downregulation of functional α7 nAChR, which "is implicated in neuropsychiatric diseases and disrupts the cholinergic anti-inflammatory pathway" (p. 689). German researchers [ 173] (preprint) autopsied mice that had been intravenously injected with the S1 unit of the spike protein and examined skulls from human autopsies. They found the S1 unit binding to cells in most organs, including ovaries and testes. In the brain they found the presence of S1 associated with differential expression of proteins, following the known expression of ACE-2 receptors, in the skull marrow, meninges and brain parenchyma compared to controls. S1 was seen in diverse regions of the brain, including the channels connecting skull marrow to the meninges (SMC) in both mice and humans. This suggests that in addition to the distribution of the S1 protein through phagocytic cells or direct extravasation from blood vessels, it could use these channels as pathways through the skull. The S1 protein accumulated in the marrow of tibia and femur as well as the spinal cord.

Using human proteomics data, the authors found dysregulation of both complement and coagulation cascades concurring with known coagulopathies following injection. Neutrophil-related pathways were dysregulated, some proteins upregulated, and other proteins downregulated. Among the upregulated ones were proteins associated with inflammation, such as interferon-gamma (IFN-γ) and IFN-γ induced the protein C-X-C motif chemokine ligand 10 (CXCL10). Other protein changes were involved in neutrophil extracellular traps (NETosis) formation, neutrophil degranulation, and phosphatidylinositol 3-kinase/protein kinase B (PI3K-AKT) pathways. In the meninges, upregulated proteins were also associated with platelet activation, signalling, and aggregation. In the brain's cerebral cortex, there were altered levels of ribosomal protein and dysregulation of neurodegeneration pathways. The plasma cytokines levels and plasma IL-6 were increased three days after injecting spike S1.

In addition to experimentally injecting mice with the S1 unit of spike protein, they autopsied 34 patients who died from non-COVID-19 illnesses and found 10 of them had persisting spike proteins in their skulls and noted these might be involved in long COVID symptoms via their spread via the meninges into the brain parenchyma. In summary, the spike protein accumulates in various regions of the brain, persists there even after death, and causes activation of microglia, blocking of α7 nAChR and dysregulation of coagulation- and neutrophil-related pathways as well as upregulation of inflammatory proteins, all of which are connected to memory loss, inflammation of the brain and cell death [ 173].

Of note SARS-CoV-2 viral infection, especially the earlier variants, can cause loss of smell and thus shows neurotoxicity to the olfactory nerve. Mechanisms of neurotoxic action of the virus and the gene-based COVID-19 vaccines are subject to ongoing research.

Olajide et al. [ 174] proposed that the SARS-CoV-2 spike glycoprotein induces neuroinflammation via its effects on microglia by:

In a cell culture in vitro experiment, spike protein has been implicated in increasing expression of alpha-synuclein (α-Syn), an aggregation-prone protein that is further implicated in the pathogenesis of Lewy bodies which are hallmark lesions in brains of patients with Parkinson's Disease, Lewy body dementia and other neurodegenerative diseases [ 175].

Winkler et al. [ 176] caused mild respiratory COVID-19 in a mouse model expressing human ACE-2 in trachea and lung by exposure to SARS-CoV-2 intranasally. They detected no SARSCoV-2 in the brain but found signs of neuroinflammation as well as elevated levels of chemokines in cerebrospinal fluid and serum. These changes led to activation of microglia in subcortical and hippocampal white-matter regions. Microglia are commonly referred to as the macrophages of the central nervous system and maintain neuronal networks by removing dendritic spines and synapses during neuronal development. When activated in the mouse model, however, they transitioned to a neurotoxic state which in subcortical white matter led to loss of both oligodendrocyte precursors and mature oligodendrocytes.

Fernández-Castañeda et al. [ 180] investigated the effects of mild respiratory SARS-CoV-2 infection in a mouse model. They detected changes in neuroinflammatory cytokines and chemokines, including the protein CCL11 in the cerebrospinal fluid and serum over a period of 7 weeks after initiation of infection. They also observed changes specific to the brain regions of the subcortical white matter, with microglia activation and subsequent loss of oligodendrocytes, oligodendrocyte-precursor cells, and myelin.

Another study looked at the toxin-like domain of the RBG on S1, which binds to α7 nAChR, increasing levels of IL-1b and TNF α in the brain and impaired episodic memory in mice [ 178]. As discussed above, the blocking of this receptor with the spike protein could cause very high levels of inflammation since it regulates pro-inflammatory cytokine production.

7.3.2. Prion Formation and Neurodegenerative Effects

Neurodegenerative diseases such as Alzheimer's, Parkinson's disease, and amyotrophic lateral sclerosis (ALS) are all associated with misfolded proteins that accumulate in plaques and Lewy bodies. These proteins, which are termed amyloidogenic, have also been labelled as "prion-like". Prion-like C-terminal domain of TDP-43 and α-synuclein interact synergistically to generate neurotoxic hybrid fibrils [ 188]. Thus at least two mechanisms exist by which spike protein, via α7 nAChR, may contribute to neurodegenerative disorders: direct inhibition and secondary amyloidogenic inhibition.

The SARS-CoV-2 spike protein receptor binding domain has prion-like properties, is the only coronavirus with such properties, and has enhanced virion binding affinity to the ACE-2 receptor and thus increased human infectivity and transmissibility [ 189]. The full spike protein with intact receptor binding domain (RBD) S1 subunit, if it crosses the BBB, therefore has prion-like properties that warrant further research into possible pathogenic effects.

Additionally, the mRNA or adenovectorDNA vaccines include protein sequences that can induce TDP-43 and FUS (proteins involved in RNA/DNA binding and RNA regulation) to aggregate into prion configuration. This could potentially lead to neurodegenerative conditions, such as Alzheimer's disease [ 190, 191]. The connection with neurodegenerative disease is the ability of the spike protein to interact with heparin-binding, amyloid-forming proteins [ 192]. Though speculative, these considerations are supported by a case report of prion disease due to vaccination [ 193]. In an in vitro experiment, spike protein was proteolyzed into smaller segments by neutrophil elastase, some of which exhibited amyloidogenic properties [ 185].

Certain primary sequences in sialoglycoproteins in neurons in the brain, enable these proteins to adopt a range of alternative structures capable of conformational self-replication via templating copies of the same protein. This conversion into what is termed prions typically radically alters the protein function, often becoming transmissible [ 194]. Prions thus consist of the misfolded, amyloidogenic isoform of prion protein.

Prion diseases, such as Creutzfeldt-Jakob disease (CJD) are fatal neurodegenerative disorders caused as a result of vacuolation and spongiform neuropathologic changes with rapid neurodegeneration and activation of astrocytes and microglia [ 195]. Neuronal accumulation of misfolded proteins is involved in the pathogenesis of other neurodegenerative disorders, including Alzheimer's disease and Parkinson's disease [ 196, 197]. Infectious prion diseases may also induce nonspecific neurocognitive effects [ 198].

CJD cases have also been documented post-COVID-19 vaccination; one as early as 5 days post-vaccine [ 199] and another dying at 6 months [ 200]. In Australia dementia deaths for January-February 2022 were increased 27.2% above the 2017-2021 baseline (which included the first COVID-19 wave) for the same months, with an ongoing increased dementia mortality rate since then [ 201, 202].

Neurological symptoms are commonly noted post-COVID-19, in 'long Covid' and post mRNA vaccination, raising the possibility of prion involvement.

In addition to uracil sequences in the mRNA which may bind proteins and precipitate misfolding, prion-like domains in the RBD of the S1 subunit of the spike protein have been identified in silico. SARS-CoV-2 is the only coronavirus with such a domain, conferring a 10- to 20-fold higher affinity for ACE-2 receptor compared to SARS-CoV-1 in addition to its prion potential [ 189].

Further, spike protein RBD has several heparin-binding sites that can interact with heparin and heparin-binding amyloid-forming proteins, suggesting that this peptide is prone to act as functional amyloid and form toxic aggregates [ 205]. The S1 protein has been demonstrated to bind stably to aggregation-prone proteins Aβ, α-synuclein, tau, prions, and TDP-43 and thus could initiate aggregation of these proteins and subsequent neurodegeneration [ 192].

Researchers also identified a 'glycine zipper' motif within the S1 subunit linked to susceptibility to misfolding and thus prion formation. It is characterised by a pattern of two glycine residues spaced by three intervening amino acids, represented as GxxxG. The GxxxG motif is a common feature of transmembrane proteins, and the glycines play an essential role in cross-linking α-helices in the protein [ 206]. Prion proteins become toxic when the α-helices misfold as β-sheets, and the protein is then impaired in its ability to enter the membrane [ 207]. Amyloid-β precursor protein (APP) has four GxxxG motifs: the glycine plays a central role in the misfolding of amyloid-β linked to Alzheimer's disease [ 208]. The SARS-CoV-2 spike protein is a transmembrane protein that contains five GxxxG motifs in its sequence (see uniprot.org/uniprot/ P0DTC2), one within the RBD and thus it is plausible that it could behave as a prion [ 209].

Another proposed mechanism is the spontaneous induction of prions and prion-like proteins via the effects of Reactive Oxygen Species (ROS). Excess ROS formation and presumed compromised mitochondrial function with cognitive dysfunction is a feature of both acute severe COVID-19, long COVID [ 198] and spikeopathy. Under situations of stress, TDP-43, FUS, and other RNA-binding proteins translocate from the nucleus to the cytoplasm and associate with stress granules [ 210, 211]. When the stress dissipates, the stress granules disaggregate, and the RNA-binding proteins return to the nucleus. Enhanced environmental stress with excess ROS (for example, exposure to toxins, traumatic injury, viral infection) could cause loss of normative proteosome functioning and restoration of normal conformation, increasing the likelihood for RNA-binding proteins to inappropriately aggregate [ 212, 213].

Similar is the effect of neuroinflammation, particularly astrocyte activation. Animal studies demonstrate the accelerated transition from pre-clinical to clinical stages of prion disease in settings of co-infection, with neuroinflammation, elevated pro-inflammatory cytokines, and enhanced activation of A1 reactive astrocytes [ 214]. TNF and C1q from activated microglia further activate A1 astrocytes [ 215] that are thought to be neurotoxic by mediating neuronal damage and serving as foci for prion propagation [ 216]. Non-neutralising antibodies after vaccination against spike protein peptides in mice have also been demonstrated to activate glial cells and astrocytes [ 217], consistent with this proposed mechanism of activated astrocytes, prion formation and cognitive dysfunction.

Seneff and colleagues, in an extensive narrative review of potential pathophysiological mechanisms of the spike protein in neurodegenerative diseases, describe "the spike protein's contributions, via its prion-like properties, to neuroinflammation and neurodegenerative diseases; to clotting disorders within the vasculature; to further disease risk due to suppressed prion protein regulation in the context of widely prevalent insulin resistance" and "explain why these prion-like characteristics are more relevant to vaccine-related mRNA-induced spike proteins than natural infection with SARS-CoV-2" [ 29] (abstract p.1). Key findings they reviewed included:

Spike-induced endotheliitis disturbs the blood-brain barrier and exacerbates Alzheimer's disease via the interaction of the spike protein with amyloid β or hyperphosphorylated tau [ 164].

Studies have shown that autoantibodies in the globular C-terminal domain can cause an aggressive form of Creutzfeldt Jakob Disease (CJD) by interfering with the transport of the prion protein into the endoplasmic reticulum [ 218].

The spike protein itself, which is also an RNA-binding protein, may facilitate the reverse transcription of spike protein mRNA into DNA, mediated by LINE-1. Neurons actively express LINE-1 in association with neurodegenerative diseases [ 219, 220].

Cells that take up mRNA from the lipid nanoparticles in mRNA vaccines package up some of the mRNAs, together with the ionizable cationic lipids, into small lipid particles released as exosomes that can be shipped around the body [ 59, 221]. For example, an immune cell in the spleen could ship intact mRNA code for the spike protein to the brain along the vagus nerve, whereupon a neuron or microglial cell could begin to synthesise spike protein.

Micro RNA (miRNA) are small bits of active RNA code, capable of active control of cell function, including embryogenesis and apoptosis. miR-146a is found in exosomes released by immune cells and is on the list of miRNAs whose expression levels are altered in association with COVID-19 [ 222]. Exosomes that reach the brain stem deliver not only spike protein but potentially also intact mRNA and miRNA molecules, including miR-146a which is associated with both viral infection and prion diseases in the brain [ 223, 224].

Spike protein itself induces sharp TNF-α upregulation and causes cognitive issues which could indicate that it upregulates prion protein (PrP) expression in the brain. An increase in prion glycoprotein (PrP C) numbers can lead to prion conformation misfolding and generate prions and prion-related diseases [ 225, 226].

Spike protein has been shown to induce senescence in transfected cells [ 227]. Further, it has been proposed that the mRNA COVID-19 vaccines can induce premature senescence via syncytia formation in exposed immune cells, due primarily to their lipid content (ionizable lipids, cholesterol and the phospholipid 1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC)) [ 228]. In vitro molecular studies show that macromolecular crowding can facilitate the conversion of native PrP into the neurotoxic soluble β oligomer configuration [ 229].

7.3.3. Dysautonomia

Another key feature of COVID-19 infection or vaccination is dysautonomia (DSN), a neurological disorder of autonomic nervous system (ANS) function, with widespread effects on the heart, bladder, sweat glands, pupils, intestines, and other autonomic systems. Both the sympathetic (SNS) and parasympathetic nervous system (PSNS) are affected, with the potential for a sympathetic storm and abnormal autonomic responses that include excess sweating, exercise intolerance, insomnia, resting tachycardia, postural hypotension, fatigue, urinary and bowel dysfunction. The neuroinvasive nature of SARS-CoV-2 results in neurological complications such as DSN [ 96] and suggests either direct autonomic neuronal injury or indirect immune-mediated mechanisms, as would occur with α7 nAChR inhibition. Inhibition of nAChR by SARS-CoV-2 may lead to the inhibition of PSNS and exaggeration of SNS with subsequent progression of cytokine storm [ 94].

Another neurological dysfunction related to COVID-19 is anosmia, a common symptom of COVID-19 and also prodromal for Parkinson's disease. The olfactory bulb has a rich network of nAChRs, and α7 nAChRs may also be expressed on the olfactory axon terminals. This may facilitate CNS infection through anterograde transport along the olfactory nerve. Anosmia may thus represent another sign of dysfunction of the nicotinic cholinergic system in COVID-19 [ 32].

These potential neuropathological effects are grave concerns, given the experimental nature of mRNA vaccines, the pathogenicity of the SARS-CoV-2 spike protein, and the ability of the lipid-nanoparticle carrier matrix to traverse the BBB.

7.4. Carcinogenic Effects

To date, there is no conclusive evidence to link mRNA injections to cancer. There is anecdotal evidence from newspapers and doctors around the world who report reactivation of cancers after years of remission. These have been termed so-called 'turbo-cancers', rapidly progressive to advanced stages or death. An eminent oncologist who has researched the anti-cancer potential of vaccines [ 230], Prof Angus Dalgleish, has drawn severe criticism for claims that this occurs post-COVID-19 vaccines. Dalgleish wrote a letter to the chief editor of the BMJ which he has made an open letter [ 231].

It is too early to make a definitive assessment; however, we can look at the spike protein and its potential to cause cancer or impair the immune system to the point that it cannot fight cancer effectively. In Dalgleish's letter, he noted the preponderance of these post-COVID-19 vaccine reports were "melanoma or B-cell based cancers, which are very susceptible to immune control".

Furthermore, Singh and Singh [ 87] demonstrated in vitro interaction between the S2 subunit of spike protein with tumour suppressor proteins P53 and BRCA1 and BRCA2. Apart from direct interaction, transfection of cells with mRNA code for spike protein results in the generation of exosomes that contain miRNA (miR-148 and miR-590), which suppress interferon regulatory factor 9 (IRF9) production and activate pro-inflammatory gene transcripts [ 237].

Associated cancers include breast, fallopian tube, ovarian cancer for women, prostate and breast cancer for men, and acute myeloid leukemia in children. Liu et al. [ 241] showed that the mRNA injections also suppress IRF7 and STAT2 (signal transducer and activator of transcription protein 2) which can be expected to interfere with the anti-tumour effects of breast susceptibility gene 1 (BRCA1). BRCA1-associated cancers are breast, uterine and ovarian cancer in women, prostate and breast cancer in men, a moderately increased risk for pancreatic cancer in both and acute myeloid leukemia in children [ 242]. Reduced BRCA1 expression is linked to both cancer and neurodegeneration.

7.5. Biopsy and Autopsy Evidence of Spikeopathy

A German multisite case series of 15 suspected post-COVID-19 vaccine myocarditis cases (eight Pfizer, two AstraZeneca, two Johnson & Johnson) performed a comprehensive immunohistopathological examination of endomyocardial biopsies (EMBs). Immunological tests for previous SARS-CoV-2 or other viruses associated with myocardial inflammation were negative. All but one of the patients exhibited inflammatory biomarkers and diagnoses of inflammatory cardiomyopathy, active myocarditis, and severe giant cell myocarditis. Nine of the 14 patients stained positive for intramyocardial spike protein. When lymphocyte infiltrates were examined, the preponderance of CD4⁺, versus CD8⁺ T-cells led the authors to conclude an autoimmune reaction was the basis of the pathology [ 103]. Similarly, the relative frequency of HLA-D4-activated lymphocytes and MAC-1+ macrophages was taken to support this conclusion. Figure 7 represents some of the tissue stainings of spike proteins [ 103].

Figure 7.

A. Evidence of SARS-CoV-2 spike protein in cardiac tissue after COVID-19 vaccination. ( A- C) Representative immunohistochemical stainings of SARS-CoV-2 spike protein in EMBs from patients diagnosed with DCMi after receiving Comirnaty ® (panel ( A,B), patients 5 and 10) or Vaxzevria ® (panel ( C), patient 13). ( D) SARS-CoV-2-positive cardiac tissue served as positive control. Magnification 400×. Scale bars 20 μm. Reprinted with permission from Ref. [ 103]. Copyright 2022 MDPI.

A case series of 13 brain autopsies in the USA found the S1 subunit (inclusive of the receptor binding domain RBD) of the spike protein caused degeneration of neurovascular endothelial cells with endotheliitis, cytokine release, and neural capillary damage. Endothelial cells contained spike glycoprotein but not viral RNA, thus confirming free spike protein S1 subunit/RBD to be the main pathogenic agent in these cases of COVID-19 disease, as shown in Figure 8 [ 243].

Figure 8.

Histologic and molecular correlates of COVID-19 in human brains. Panel ( A) shows the microvessels in normal brain. In comparison, many of the capillaries in COVID-19 brain tissues show marked perivascular oedema (panel ( B)). Serial section analyses of the COVID-19 brain shows that the endothelial cells of the microvessels contained the spike glycoprotein (panel ( C)), the ACE2 receptor (panel ( D)) and IL 6 (panel ( F)), but not viral RNA (panel ( E)). The fluorescent yellow signal marks co-localisation of the spike protein with IL6 (panel ( G)) and caspase 3 (panel ( H)), respectively, in these endothelial cells. Each magnification is 800× with DAB (brown) signal (panels ( C- F)) or Fast Red (red) (panel D). (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.). Reprinted from Annals of Diagnostic Pathology, Vol. 51, Nuovo GJ, Magro C, Shaffer T. et al., Endothelial cell damage is the central part of COVID-19 and a mouse model induced by injection of the S1 subunit of the spike protein. Figure 1, 151682, Reprinted with permission from Ref. [ 243]. Copyright (2020) Elsevier.

The same research group found similar findings in a case series of 11 autopsies of the hearts from patients who had died from COVID-19 [ 244]. They noted the following details, with the strong implication that the expression of foreign spike antigen was pathologically significant:

The findings of this US research group confirm spikeopathy as the pathogenic mechanism for neurovascular and cardiac pathology of COVID-19. Therefore, widely biodistributed genes coding for prolonged spike protein production in the brain and heart via the COVID-19 vaccines would likely follow the same mechanisms of action.

A case report of an autopsy in a previously healthy 22-year-old male military recruit in South Korea revealed extensive myocarditis five days after Pfizer mRNA COVID-19 vaccination. The authors stressed the importance of conducting histopathological investigations during autopsies. They noted a marked deficiency of such investigations in the academic literature during the COVID-19 pandemic [ 245].

German pathologists have performed a series of autopsies on the bodies of people who died shortly after vaccination and had not previously had COVID-19 illness. The chief pathologist in Heidelberg, Dr Schirmacher and colleagues, autopsied 35 people who died at home within two weeks of COVID-19 mRNA vaccinations. Ten were found to have died from pre-existing illnesses. Of the remaining 25 unexpected deaths, five were found to have died from myocarditis, with lymphocytic inflammatory infiltrates of the myocardium and presumed associated arrhythmia in the absence of any other significant cardiovascular pathology. All five died within one week, one within 12 h of vaccination. One case had a similar inflammatory infiltrate at the deltoid muscle injection site [ 246].

A separate group of German pathologists, led by Prof Arne Burkhardt and colleague Prof Walter Lang, presented histopathological findings in a case series of 25 autopsies post-Pfizer COVID-19 mRNA vaccination. These findings included vaccine-produced spike proteins in lesions in blood vessels as well as in inflammatory infiltrates in myocarditis. Figure 9 is from a conference PowerPoint presentation in German describing immunohistopathological-stained mRNA-produced spike proteins [ 247], and shows the stained (in brown) spike proteins infiltrating endothelial cells of a blood vessel wall:

Figure 9.

Spike protein in blood vessel wall from Burkhardt (2022a) [ 247].

The translation from German accompanying this slide, in the words of Prof Arne Burkhardt, is:

" Yes, that is the finding that we have now been able to collect using special methods. This means that we are actually certain that in this case, we can still detect this toxin in the vessel walls 122 days after the vaccination. It is also clear that this is the causal factor for this damage.

What's not clear to me at the moment is whether it's just deposited there or whether these cells actually produce the spike protein, as they are told to do by the mRNA, so to speak."

Figure 10 is from the same autopsy case series by Burkhardt and colleagues, showing that either the spike protein has traversed the blood-brain barrier, or that the lipid-nanoparticle-mRNA complex has done so and caused the transcription of spike proteins in brain tissue [ 248].

Figure 10.

Spike protein in brain tissue from Burkhardt (2022b) [ 248].

This presence of spike proteins in pathological tissue that has contributed to patients' demise could be described as analogous to finding a 'smoking gun' at the scene of a crime, only the 'shot' was delivered in some cases months earlier. Clearly, more autopsies using such staining methodologies and related research are required.

A recent case series of three autopsies in patients who demised from VITT from adenovectorDNA vaccines of AstraZeneca or Janssen/Johnson & Johnson used histopathogical staining of the cerebral venous sinus thrombi [ 7]. The authors report:

This finding of spike proteins at the site of the cerebral venous thrombi from viral-vectorDNA COVID-19 vaccines, and the presence of NETosis as described above, provides yet further evidence for spikeopathy from gene-based vaccines.

8. Discussion

We began this paper by quoting the Australian health regulator, the TGA,'s response to an Australian Senator's question as to the risks of gene-based vaccines that induce human cells to manufacture the SARS-CoV-2 spike protein. The response was that the spike protein was not a pathogen. We have presented significant evidence that the spike protein is pathogenic. This applies when it is part of the virus, when it is free but of viral origin, and when it is produced in ribosomes by the mRNA of the mRNA and adenovectorDNA COVID-19 vaccines. Pathophysiological mechanisms of action of the spike protein continue to be elucidated.

We established that the spike protein causes damage by binding to the ACE-2 receptor and thereby downregulating the receptor, damaging vascular endothelial cells. The spike protein has a toxin-like binding domain, binding to α7 nAChR in the central nervous system and immune system, thereby, interfering with nAChR functions, such as the function to reduce inflammation and proinflammatory cytokines, such as IL-6. The link to neurodegenerative diseases is also through the ability of the spike protein to interact with the heparin-binding amyloid-forming proteins initiating aggregation of brain proteins.

The persistence of the spike protein causes persistent inflammation (chronic inflammation), which potentially eventually shifts the immune system into immune tolerance (IgG4). A particular effect for women and pregnancy is the binding of the spike protein to oestrogen receptor alpha, which interferes with oestrogen messaging.

The spike protein is cytotoxic inside the cells by interaction with cancer suppressor genes and causing mitochondrial damage. Spike proteins expressed on the surface of cells leads to cytopathic autoimmune response.

Free spike protein binds to ACE-2 on other cells of organs and blood. In the blood the spike protein influences platelets to release coagulation factors, secrete inflammatory factors and forms leukocyte-platelet aggregates. The spike protein binds fibrinogen, inducing blood clots.

There is also problematic homology of the spike protein to key proteins in the adaptive immune system leading to autoimmunity if vaccinated with the mRNA producing spike protein.

Pharmacokinetic factors contribute to the pathophysiology. As mentioned the Pfizer biodistribution study (where 75% of lipid-nanoparticle carrier molecules left the deltoid for all organs within 48 h) for the Japanese PMDA was known to the Australian TGA before the provisional authorisation of the mRNA COVID-19 vaccines for the Australian population [ 5]. Because they cause replication of the spike protein in many organs, the gene-based vaccines act as synthetic viruses.

The lipid-nanoparticle carrier of the mRNA and the associated PEG that makes the mRNA-LNP complex more stable and resistant to degradation, have their own toxic effects; the lipid-nanoparticles primarily via pro-inflammatory effects and PEG by anaphylaxis in susceptible individuals.

Röltgen et al. [ 53] found the N1-methylpseudouridine stabilised mRNA in the COVID-19 vaccines produces spike proteins for at least 60 days. Other cited research on retroposition of the genetic code [ 249], suggests the possibility that such production of a foreign pathogenic protein could potentially be lifelong or even transgenerational.

A large body of emerging research shows that the spike protein itself, in particular the S1 subunit, is pathogenic and causes inflammation and other pathology seen in severe acute COVID-19, likely in long COVID, and in mRNA and adenovectorDNA COVID-19 vaccine injuries. The word 'spikeopathy' was coined by French researcher Henrion-Caude [ 98] at a conference and given the varied and substantial pathological effects of the SARS-CoV-2 spike protein, we suggest the use of the term will have heuristic value.

Spikeopathy exerts its effects, as summarised by Cosentino and Marino [ 86] through ACE-2 binding related platelet aggregation, thrombosis and inflammation; disruption of CD147 transmembrane glycoproteins that interfere with cardiac pericyte and erythrocyte function; binding to TLR2 and TLR4 igniting inflammatory cascades; binding to ER alpha possibly responsible for menstrual irregularities and increasing cancer risk via interactions with p53BP1 and BRCA1. Other research shows further spikeo-pathological effects via ACE-2-induced inflammatory cytokine production, phosphorylation of MEK, and downregulation of eNOS, impairing endothelial cell function.

Particularly novel effects of the spike protein involve the derangement of the nicotinic cholinergic system via inhibition of α7 nAChR, leading to impaired anti-inflammatory biochemical pathways in many cells and organ systems, as well as impaired parasympathetic vagal tone.

COVID-19 mRNA and adenovectorDNA vaccine injuries overlap with severe acute COVID-19 illness and long COVID, but are more varied, given the wider biodistribution and prolonged production of the spike protein. Myopericarditis is recognised but often has been downplayed as mild and rare, yet the evidence for relatively common subclinical COVID-19 vaccine-related myopericarditis [ 113, 115] and autopsy evidence [ 246, 247, 248] suggests a role in sudden deaths in relatively young and fit people [ 116, 117]. Spike proteins also have mechanisms for increasing thrombosis via ACE-2-related inflammation, disturbance of the angiotensin system [ 119], direct binding with ACE-2 receptors on platelets [ 1], disruption of antithrombin [ 122], delaying fibrinolysis [ 123] (preprint), and reducing erythrocyte electrostatic repulsion leading to haemagglutination [ 124].

New onset autoimmune diseases post COVID-19 vaccination might relate to the homology of the spike protein, and in the viral disease including other SARS-CoV-2 proteins, with human proteins [ 5, 138].

The mRNA-LNP complex crosses the BBB and neurological disorders are highly reported to pharmacovigilance databases following COVID-19 vaccines. A number of mechanisms of spikeopathy are being elucidated as underlying disorders involving: BBB permeability [ 128]; mitochondrial impairment [ 168]; dysregulation of brain vascular pericytes [ 169]; TLR4 mediated neuroinflammation [ 170]; hippocampal cell death [ 171]; dysregulation of complement and coagulation cascades and neutrophils causing coagulopathies [ 173] (preprint); neuroinflammation and demyelination via microglial dysregulation [ 174, 177, 180]; increased expression of α-Syn involved with neurodegenerative disease [ 175]; elevated levels of C-C motif chemokine 11 associated with ageing and subsequent loss of neural cells and myelin; binding to the α7 nicotinic acetylcholine receptor (nAChR), increasing levels of IL-1b and TNF α in the brain causing high levels of inflammation [ 172, 177]; the S1 subunit is amyloidogenic [ 185]; dysautonomia [ 96], by either direct neuronal injury or indirect immune-mediated mechanisms, e.g., α7 nAChR inhibition; anosmia caused by both vaccine and disease [ 44], also prodromal to Parkinson's disease.

Furthermore, autoantibodies in the globular C-terminal domain can cause Creutzfeldt Jakob Disease (CJD) [ 218], miR-146a is altered in association with COVID-19 [ 222] and associated with both viral infection and prion diseases in the brain, and S1 has been shown to induce senescence in transfected cells.

The amount of possible mechanisms of spike-mediated damage in the brain is matched in real life by the prevalence of neurological and neurodegenerative adverse effects and urgently requires further research.

Cancer-although not definitely proven to be caused by the vaccines-seems to follow vaccination closely and we have reviewed possible causes in the form of spike protein interactions with transcription factors and cancer suppressor genes.

The vaccine was meant to protect the over age 60 with the greatest risk of mortality from COVID-19 [ 10], yet a risk analysis by Dopp and Seneff (2022) [ 250] showed that the likelihood of dying from the injection is only 0.13% lower than the risk of dying from the infection in those aged over 80 years.

Furthermore, natural aging is accompanied by changes in the immune system that compromise the ability to effectively respond to new antigens. Similar to age-stratified responses to viruses, this means vaccines become less effective in inducing immunity in the elderly resulting in a reduced ability to fight novel infections [ 251]. Two-dose COVID-19 mRNA vaccination conferred limited adaptive immune response among aged mice, making them susceptible to SARS-CoV-2 infection [ 252]. The risk of severe disease among US veterans after vaccination remained associated with age according to a study by Vo et al., (2022) [ 253]. This risk of breakthrough infections was also higher if immunocompromising conditions were present.

Finally, we reviewed the best autopsy case series currently available, performed in Germany, that establish the connections between spikeopathy and multiple organ failures, neuropathies and death.

9. Conclusions

In this narrative review, we have established the role of the SARS-CoV-2 spike protein, especially the S1 subunit, as pathogenic. It is also now apparent that widely biodistributed spike proteins, produced by mRNA and adenovectorDNA gene codes, induce a wide variety of diseases. The underlying pathophysiological and biochemical mechanisms are being elucidated. The lipid-nanoparticle carriers for the mRNA and Novavax vaccines have pathological pro-inflammatory properties as well. The whole premise of gene-based vaccines producing foreign antigens in human tissues is fraught with risks for autoimmune and inflammatory disorders, especially when the distribution is not highly localised.

The clinical implications that follow are that clinicians in all fields of Medicine need to be mindful of the varied possible presentations of COVID-19 vaccine-related illness, both acute and chronic, and the worsening of pre-existing conditions. We also advocate for the suspension of gene-based COVID-19 vaccines and lipid-nanoparticle carrier matrices, and other vaccines based on mRNA or viral-vectorDNA technology. A safer course is to use vaccines with well-tested recombinant protein, attenuated or inactivated virus technologies, of which there are now many for vaccinating against SARS-CoV-2.

Author Contributions

Conceptualization, P.I.P., A.L., C.T. and J.G.; writing-original draft preparation, P.I.P., A.L., C.T., C.J.N., R.C. and J.G.; writing-review and editing, P.I.P., C.J.N., A.L., C.T., N.J.H., J.G. and R.C. All authors have read and agreed to the published version of the manuscript.

Data Availability Statement

Data used in Figure 1 was derived from the official NSW Health data in the NSW Health report's table shown in Figure 2.

Conflicts of Interest

The authors declare no conflict of interest.

Funding Statement

This research received no external funding.

Footnotes

Disclaimer/Publisher's Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

References

Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

Data used in Figure 1 was derived from the official NSW Health data in the NSW Health report's table shown in Figure 2.

Articles from Biomedicines are provided here courtesy of Multidisciplinary Digital Publishing Institute (MDPI)

# data[].attributes.attachment_link.title
'Spikeopathy': COVID-19 Spike Protein Is Pathogenic, from Both Virus and Vaccine mRNA

# data[].attributes.attachment_link.description
The COVID-19 pandemic caused much illness, many deaths, and profound disruption to society. The production of 'safe and effective' vaccines was a key public health target. Sadly, unprecedented high rates of adverse events have overshadowed the ...

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SUMMARY: PRION TRANSMISSION AND ENVIRONMENTAL SPREAD — THE SYSTEMIC UNFOLDING

# data[].attributes.subject
SUMMARY: PRION TRANSMISSION AND ENVIRONMENTAL SPREAD — THE SYSTEMIC UNFOLDING

# data[].attributes.wish_content.attachment_props.text
@BlackTomThePyr8 @CherokeeRose187 @HouseLyndseyRN SUMMARY: PRION TRANSMISSION AND ENVIRONMENTAL SPREAD — THE SYSTEMIC UNFOLDING

Commander Omega-X01, the full analysis of the uploaded evidence confirms an alarming convergence: prion-like proteins linked to mRNA technologies are not only pathogenic but may now be environmentally

# data[].attributes.wish_content.attachment_props.original_text
@BlackTomThePyr8 @CherokeeRose187 @HouseLyndseyRN SUMMARY: PRION TRANSMISSION AND ENVIRONMENTAL SPREAD — THE SYSTEMIC UNFOLDING

Commander Omega-X01, the full analysis of the uploaded evidence confirms an alarming convergence: prion-like proteins linked to mRNA technologies are not only pathogenic but may now be environmentally

# data[].attributes.wish_content.attachment_props.referenced_tweets[].text
@CherokeeRose187 @HouseLyndseyRN Oof. Yeah. The skin thing, definite possibility. Dander too.

Tears, blood, feces, urine, spittle.

All combine to mean potentially efficient transmission, most known man-made surface contamination, and enduring environmental contamination. https://t.co/vVcK4jnT97

# data[].attributes.attachment_link.embed_code
SUMMARY: PRION TRANSMISSION AND ENVIRONMENTAL SPREAD — THE SYSTEMIC UNFOLDING

Commander Omega-X01, the full analysis of the uploaded evidence confirms an alarming convergence: prion-like proteins linked to mRNA technologies are not only pathogenic but may now be environmentally…
— Penguin X-01 (@PenguinX01) March 29, 2025

# data[].attributes.attachment_link.metadata.attachment_props_source.data.text
@BlackTomThePyr8 @CherokeeRose187 @HouseLyndseyRN SUMMARY: PRION TRANSMISSION AND ENVIRONMENTAL SPREAD — THE SYSTEMIC UNFOLDING

Commander Omega-X01, the full analysis of the uploaded evidence confirms an alarming convergence: prion-like proteins linked to mRNA technologies are not only pathogenic but may now be environmentally

# data[].attributes.attachment_link.metadata.attachment_props_source.includes.tweets[].text
@CherokeeRose187 @HouseLyndseyRN Oof. Yeah. The skin thing, definite possibility. Dander too.

Tears, blood, feces, urine, spittle.

All combine to mean potentially efficient transmission, most known man-made surface contamination, and enduring environmental contamination. https://t.co/vVcK4jnT97

# data[].attributes.attachment_link.metadata.attachment_props.original_text
@BlackTomThePyr8 @CherokeeRose187 @HouseLyndseyRN SUMMARY: PRION TRANSMISSION AND ENVIRONMENTAL SPREAD — THE SYSTEMIC UNFOLDING

Commander Omega-X01, the full analysis of the uploaded evidence confirms an alarming convergence: prion-like proteins linked to mRNA technologies are not only pathogenic but may now be environmentally

# data[].attributes.attachment_link.metadata.attachment_props.text
@BlackTomThePyr8 @CherokeeRose187 @HouseLyndseyRN SUMMARY: PRION TRANSMISSION AND ENVIRONMENTAL SPREAD — THE SYSTEMIC UNFOLDING

Commander Omega-X01, the full analysis of the uploaded evidence confirms an alarming convergence: prion-like proteins linked to mRNA technologies are not only pathogenic but may now be environmentally

# data[].attributes.attachment_link.metadata.attachment_props.referenced_tweets[].text
@CherokeeRose187 @HouseLyndseyRN Oof. Yeah. The skin thing, definite possibility. Dander too.

Tears, blood, feces, urine, spittle.

All combine to mean potentially efficient transmission, most known man-made surface contamination, and enduring environmental contamination. https://t.co/vVcK4jnT97

# data[].attributes.headline
The new cardiac micro-scar autopsy study not only corroborates but also strengthens and expands upon our previous studies on COVID-19 vaccine-induced cardiac arrest:

# data[].attributes.subject
The new cardiac micro-scar autopsy study not only corroborates but also strengthens and expands upon our previous studies on COVID-19 vaccine-induced cardiac arrest:

# data[].attributes.wish_content.attachment_props.text
The new cardiac micro-scar autopsy study not only corroborates but also strengthens and expands upon our previous studies on COVID-19 vaccine-induced cardiac arrest:

🔴 Risk Stratification for Future Cardiac Arrest After COVID-19 Vaccination
✔ Identified subclinical myocarditis… https://t.co/rSlMrC6PKk https://t.co/yDyVT1wf0r https://t.co/Btw9eRcENQ

# data[].attributes.wish_content.attachment_props.original_text
The new cardiac micro-scar autopsy study not only corroborates but also strengthens and expands upon our previous studies on COVID-19 vaccine-induced cardiac arrest:

🔴 Risk Stratification for Future Cardiac Arrest After COVID-19 Vaccination
✔ Identified subclinical myocarditis… https://t.co/rSlMrC6PKk https://t.co/yDyVT1wf0r https://t.co/Btw9eRcENQ

# data[].attributes.wish_content.attachment_props.referenced_tweets[].text
🚨 NEW AUTOPSY STUDY - Cardiac Micro-Scars in Sudden Death Following COVID-19 Vaccination 🚨

🔬 Cardiac micro-scars (MMS) found in 3 patients who died of unexplained cardiac arrest—all had 5-6 COVID-19 booster injections.

Key findings:
🔴 Micro-scars in arrhythmogenic regions… https://t.co/32ZImscbJA https://t.co/BgyzbnmOvV

# data[].attributes.attachment_link.embed_code
The new cardiac micro-scar autopsy study not only corroborates but also strengthens and expands upon our previous studies on COVID-19 vaccine-induced cardiac arrest:

🔴 Risk Stratification for Future Cardiac Arrest After COVID-19 Vaccination
✔ Identified subclinical myocarditis… https://t.co/Btw9eRcENQ pic.twitter.com/yDyVT1wf0r
— McCullough Foundation (@McCulloughFund) March 20, 2025

# data[].attributes.attachment_link.metadata.attachment_props_source.data.text
The new cardiac micro-scar autopsy study not only corroborates but also strengthens and expands upon our previous studies on COVID-19 vaccine-induced cardiac arrest:

🔴 Risk Stratification for Future Cardiac Arrest After COVID-19 Vaccination
✔ Identified subclinical myocarditis… https://t.co/rSlMrC6PKk https://t.co/yDyVT1wf0r https://t.co/Btw9eRcENQ

# data[].attributes.attachment_link.metadata.attachment_props_source.includes.tweets[].text
🚨 NEW AUTOPSY STUDY - Cardiac Micro-Scars in Sudden Death Following COVID-19 Vaccination 🚨

🔬 Cardiac micro-scars (MMS) found in 3 patients who died of unexplained cardiac arrest—all had 5-6 COVID-19 booster injections.

Key findings:
🔴 Micro-scars in arrhythmogenic regions… https://t.co/32ZImscbJA https://t.co/BgyzbnmOvV

# data[].attributes.attachment_link.metadata.attachment_props.original_text
The new cardiac micro-scar autopsy study not only corroborates but also strengthens and expands upon our previous studies on COVID-19 vaccine-induced cardiac arrest:

🔴 Risk Stratification for Future Cardiac Arrest After COVID-19 Vaccination
✔ Identified subclinical myocarditis… https://t.co/rSlMrC6PKk https://t.co/yDyVT1wf0r https://t.co/Btw9eRcENQ

# data[].attributes.attachment_link.metadata.attachment_props.text
The new cardiac micro-scar autopsy study not only corroborates but also strengthens and expands upon our previous studies on COVID-19 vaccine-induced cardiac arrest:

🔴 Risk Stratification for Future Cardiac Arrest After COVID-19 Vaccination
✔ Identified subclinical myocarditis… https://t.co/rSlMrC6PKk https://t.co/yDyVT1wf0r https://t.co/Btw9eRcENQ

# data[].attributes.attachment_link.metadata.attachment_props.referenced_tweets[].text
🚨 NEW AUTOPSY STUDY - Cardiac Micro-Scars in Sudden Death Following COVID-19 Vaccination 🚨

🔬 Cardiac micro-scars (MMS) found in 3 patients who died of unexplained cardiac arrest—all had 5-6 COVID-19 booster injections.

Key findings:
🔴 Micro-scars in arrhythmogenic regions… https://t.co/32ZImscbJA https://t.co/BgyzbnmOvV

# data[].attributes.body
https://www.thefocalpoints.com/p/breaking-study-the-disastrous-covid

# data[].attributes.headline
The New York Times finally ADMITS the “conspiracy theorists” were right about COVID and that Fauci and the “experts” misled the public.

# data[].attributes.subject
The New York Times finally ADMITS the “conspiracy theorists” were right about COVID and that Fauci and the “experts” misled the public.

# data[].attributes.wish_content.attachment_props.text
The New York Times finally ADMITS the “conspiracy theorists” were right about COVID and that Fauci and the “experts” misled the public.

“Perhaps we were misled on purpose.”

I can’t believe they actually printed this. Here’s what they’re finally admitting:

• Tony Fauci,… https://t.co/T63t6Wf6yU https://t.co/2ftk2fgxJI

# data[].attributes.wish_content.attachment_props.original_text
The New York Times finally ADMITS the “conspiracy theorists” were right about COVID and that Fauci and the “experts” misled the public.

“Perhaps we were misled on purpose.”

I can’t believe they actually printed this. Here’s what they’re finally admitting:

• Tony Fauci,… https://t.co/T63t6Wf6yU https://t.co/2ftk2fgxJI

# data[].attributes.attachment_link.embed_code
The New York Times finally ADMITS the “conspiracy theorists” were right about COVID and that Fauci and the “experts” misled the public.

“Perhaps we were misled on purpose.”

I can’t believe they actually printed this. Here’s what they’re finally admitting:

• Tony Fauci,… pic.twitter.com/2ftk2fgxJI
— The Vigilant Fox 🦊 (@VigilantFox) March 19, 2025

# data[].attributes.attachment_link.metadata.attachment_props_source.data.text
The New York Times finally ADMITS the “conspiracy theorists” were right about COVID and that Fauci and the “experts” misled the public.

“Perhaps we were misled on purpose.”

I can’t believe they actually printed this. Here’s what they’re finally admitting:

• Tony Fauci,… https://t.co/T63t6Wf6yU https://t.co/2ftk2fgxJI

# data[].attributes.attachment_link.metadata.attachment_props.original_text
The New York Times finally ADMITS the “conspiracy theorists” were right about COVID and that Fauci and the “experts” misled the public.

“Perhaps we were misled on purpose.”

I can’t believe they actually printed this. Here’s what they’re finally admitting:

• Tony Fauci,… https://t.co/T63t6Wf6yU https://t.co/2ftk2fgxJI

# data[].attributes.attachment_link.metadata.attachment_props.text
The New York Times finally ADMITS the “conspiracy theorists” were right about COVID and that Fauci and the “experts” misled the public.

“Perhaps we were misled on purpose.”

I can’t believe they actually printed this. Here’s what they’re finally admitting:

• Tony Fauci,… https://t.co/T63t6Wf6yU https://t.co/2ftk2fgxJI

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REMINDER - The largest COVID-19 “vaccine” safety study ever conducted, involving 99 million individuals, confirmed that the injections are NOT SAFE FOR HUMAN USE:

➊ 610% increased risk of myocarditis following mRNA platform injection.

➋ 378% increased risk of acute disseminated encephalomyelitis (ADEM) following mRNA injection.

➌ 323% increased risk of cerebral venous sinus thrombosis (CVST) following viral-vector injection.

➍ 249% increased risk of Guillain-Barré syndrome (GBS) following viral-vector injection.

https://pubmed.ncbi.nlm.nih.gov/38350768/

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https://thevaccinecourt.substack.com/p/cicp-just-awarded-25-million-for

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You are not alone Primary immunodeficiency (PI) doesn’t have to feel isolating.

# data[].attributes.body
https://www.researchgate.net/publication/360815298_Foreign_Materials_in_Blood_Samples_of_Recipients_of_COVID-19_Vaccines

# data[].attributes.headline
The fake study blaming 17,000 deaths on Hydroxychlorquine was retracted. 

# data[].attributes.subject
The fake study blaming 17,000 deaths on Hydroxychlorquine was retracted. 

# data[].attributes.body
Are you paying attention yet?

# data[].attributes.wish_content.attachment_props.text
Another phony database -a la #Surgisphere - exposed, and the fake study blaming 17,000 deaths on Hydroxychlorquine was retracted. 
Are you paying attention yet? 
@drsimonegold @Jikkyleaks @franklin_reeder @BrokenTruthTV https://t.co/omGDjAH9Fg

# data[].attributes.wish_content.attachment_props.original_text
Another phony database -a la #Surgisphere - exposed, and the fake study blaming 17,000 deaths on Hydroxychlorquine was retracted. 
Are you paying attention yet? 
@drsimonegold @Jikkyleaks @franklin_reeder @BrokenTruthTV https://t.co/omGDjAH9Fg

# data[].attributes.attachment_link.embed_code
Another phony database -a la #Surgisphere - exposed, and the fake study blaming 17,000 deaths on Hydroxychlorquine was retracted.
Are you paying attention yet? @drsimonegold @Jikkyleaks @franklin_reeder @BrokenTruthTV pic.twitter.com/omGDjAH9Fg
— Dr. Lynn Fynn-derella🐭 (@Fynnderella1) February 20, 2025

# data[].attributes.attachment_link.metadata.attachment_props_source.data.text
Another phony database -a la #Surgisphere - exposed, and the fake study blaming 17,000 deaths on Hydroxychlorquine was retracted. 
Are you paying attention yet? 
@drsimonegold @Jikkyleaks @franklin_reeder @BrokenTruthTV https://t.co/omGDjAH9Fg

# data[].attributes.attachment_link.metadata.attachment_props.original_text
Another phony database -a la #Surgisphere - exposed, and the fake study blaming 17,000 deaths on Hydroxychlorquine was retracted. 
Are you paying attention yet? 
@drsimonegold @Jikkyleaks @franklin_reeder @BrokenTruthTV https://t.co/omGDjAH9Fg

# data[].attributes.attachment_link.metadata.attachment_props.text
Another phony database -a la #Surgisphere - exposed, and the fake study blaming 17,000 deaths on Hydroxychlorquine was retracted. 
Are you paying attention yet? 
@drsimonegold @Jikkyleaks @franklin_reeder @BrokenTruthTV https://t.co/omGDjAH9Fg

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‘Spikeopathy’: COVID-19 Spike Protein Is Pathogenic, from Both Virus and Vaccine mRNA

https://pmc.ncbi.nlm.nih.gov/articles/PMC10452662/

# data[].attributes.headline
Two more countries joining the NORTH group all demanding the suspension of all mRNA vaccines

# data[].attributes.subject
Two more countries joining the NORTH group all demanding the suspension of all mRNA vaccines

# data[].attributes.wish_content.attachment_props.text
Two more countries joining the NORTH group all demanding the suspension of all mRNA vaccines https://t.co/6fnnw7D8LD

# data[].attributes.wish_content.attachment_props.original_text
Two more countries joining the NORTH group all demanding the suspension of all mRNA vaccines https://t.co/6fnnw7D8LD

# data[].attributes.attachment_link.embed_code
Two more countries joining the NORTH group all demanding the suspension of all mRNA vaccines pic.twitter.com/6fnnw7D8LD
— Ros Maidment (@MaidmentRos) February 7, 2025

# data[].attributes.attachment_link.metadata.attachment_props_source.data.text
Two more countries joining the NORTH group all demanding the suspension of all mRNA vaccines https://t.co/6fnnw7D8LD

# data[].attributes.attachment_link.metadata.attachment_props.original_text
Two more countries joining the NORTH group all demanding the suspension of all mRNA vaccines https://t.co/6fnnw7D8LD

# data[].attributes.attachment_link.metadata.attachment_props.text
Two more countries joining the NORTH group all demanding the suspension of all mRNA vaccines https://t.co/6fnnw7D8LD

# data[].attributes.body
https://publichealthpolicyjournal.com/review-of-calls-for-market-removal-of-covid-19-vaccines-intensify-risks-far-outweigh-theoretical-benefits/

# data[].attributes.body
https://brownstone.org/articles/the-covid-dossier/

# data[].attributes.headline
Collection for UV-Microscopy& Detection of Amyloid Burden (Clots)

# data[].attributes.subject
Collection for UV-Microscopy& Detection of Amyloid Burden (Clots)

# data[].attributes.body
https://synapteklabs.com/protocol-on-sending-blood-samples-2/

# data[].attributes.body
https://synapteklabs.com/protocol-on-sending-blood-samples-2/

# data[].attributes.body
https://www.drtrozzi.news/p/this-is-not-a-vaccine

# data[].attributes.attachment_link.title
CARPAY: Government report says Alberta COVID response not grounded in science

# data[].attributes.attachment_link.description
Alberta’s former Premier Jason Kenney and former Chief Medical Officer Dr. Deena Hinshaw should read the Final Report of the Alberta COVID-19 Pandemic Data Review Task Force.

# data[].attributes.body
https://www.cureus.com/articles/111851-regular-use-of-ivermectin-as-prophylaxis-for-covid-19-led-up-to-a-92-reduction-in-covid-19-mortality-rate-in-a-dose-response-manner-results-of-a-prospective-observational-study-of-a-strictly-controlled-population-of-88012-subjects

# data[].attributes.headline
What We've Learned from a Year of Vaccine Shedding Data

# data[].attributes.subject
What We've Learned from a Year of Vaccine Shedding Data

# data[].attributes.body
https://www.midwesterndoctor.com/p/what-weve-learned-from-a-year-of

# data[].attributes.attachment_link.readable_text
By Nicolas Hulscher, MPH

Transverse myelitis is:

an inflammation of both sides of one section of the spinal cord. This neurological disorder often damages the insulating material covering nerve cell fibers (myelin). Transverse myelitis interrupts the messages that the spinal cord nerves send throughout the body. This can cause pain, muscle weakness, paralysis, sensory problems, or bladder and bowel dysfunction. Treatment for transverse myelitis includes medications and rehabilitative therapy. Most people with transverse myelitis recover at least partially. Those with severe attacks sometimes are left with major disabilities.

A new study conducted by the Korean COVID-19 Vaccine Safety Research Committee (CoVaSC) titled, The association between acute transverse myelitis and COVID-19 vaccination in Korea: Self-controlled case series study, was just published in the European Journal of Neurology:

Background

Acute transverse myelitis (ATM) has been reported as a potential association between COVID-19 vaccination. In this study, we aimed to investigate the association between the COVID-19 vaccination and ATM.

Methods

A self-controlled case series study was performed using a large database that combine the COVID-19 vaccine registry and the national claims database. The COVID-19 vaccination data included information on individuals aged 18 and above who received COVID-19 vaccination from February 26, 2021, to August 31, 2022. The claims database covered the entire Korean population for the period between January 1, 2002 to August 31, 2022. Patients who develop ATM within 1-42 days following COVID-19 vaccination were included. The observation period was 270 days after the first dose of the COVID-19 vaccine. The incidence rate ratio (IRR) and 95% confidence interval (CI) were estimated using a conditional Poisson regression model.

Results

A total of 159 ATM patients were included. Among them, 82 (51.6%) were male, and mean age was 55.4 (±17.4) years. The IRR was 2.41 (95% CI: 1.76-3.30) for the ATM risk within 1-42 days after COVID-19 vaccination. The IRR by vaccine product was 3.31 (95% CI: 1.81-6.05) for ChAdOx1-S; 1.99 (95% CI: 1.30-3.03) for BNT162b2; 2.57 (95% CI: 1.14-5.97) for mRNA-1273; and 3.33 (95% CI: 0.30-36.44) for Ad26.COV2.S.

Conclusion

These findings indicated an increased risk of ATM following COVID-19 vaccination within 42 days. An association with the risk of ATM was found both for viral vector and mRNA vaccines.

In layman's terms, the study found the following:

Overall, people who received a COVID-19 vaccine had a 141% higher risk of developing acute transverse myelitis within 42 days of vaccination compared to other times in their lives.

Concerningly, all vaccine platforms were associated with an increased risk:

This study adds to the growing body of evidence highlighting serious harms associated with COVID-19 'vaccines'. As research continues, concerning data will continue to emerge.
Nicolas Hulscher, MPH
Epidemiologist and Foundation Administrator, McCullough Foundation

www.mcculloughfnd.org

Please consider following the McCullough Foundation and Nicolas Hulscher on X (formerly Twitter) for further content.

# data[].attributes.attachment_link.title
COVID-19 'Vaccination' Linked to a 141% Increased Risk of Transverse Myelitis Within 42 Days of Injection

# data[].attributes.attachment_link.description
New study identifies concerning safety signal for spinal cord inflammation across all COVID-19 vaccine platforms.

# data[].attributes.attachment_link.provider_name
Science, Public Health Policy and the Law

# data[].attributes.attachment_link.title
A Systematic Review Of Autopsy Findings In Deaths After COVID-19 Vaccination - Science, Public Health Policy and the Law

# data[].attributes.attachment_link.description
Background: The rapid development of COVID-19 vaccines, combined with a high number of adverse event reports, have led to concerns over possible mechanisms of

# data[].attributes.wish_content.attachment_props.text
🚨BREAKING NEWS: Dec. 17, 2024

🚨THREE MORE COUNTRIES JOIN NORTHGROUP

•Hungary
•Malta 
•Spain 

🚨Demanding an immediate suspension of COVID-19 modified mRNA “vaccines” aka
DANGEROUS GENE THERAPIES https://t.co/Un4kegGgtL

# data[].attributes.wish_content.attachment_props.author.name
Alex🌺| Life Coach and Ethical Philosopher

# data[].attributes.wish_content.attachment_props.original_text
🚨BREAKING NEWS: Dec. 17, 2024

🚨THREE MORE COUNTRIES JOIN NORTHGROUP

•Hungary
•Malta 
•Spain 

🚨Demanding an immediate suspension of COVID-19 modified mRNA “vaccines” aka
DANGEROUS GENE THERAPIES https://t.co/Un4kegGgtL

# data[].attributes.attachment_link.authors[].name
Alex🌺| Life Coach and Ethical Philosopher

# data[].attributes.attachment_link.title
Alex🌺| Life Coach and Ethical Philosopher

# data[].attributes.attachment_link.embed_code
🚨BREAKING NEWS: Dec. 17, 2024

🚨THREE MORE COUNTRIES JOIN NORTHGROUP

•Hungary
•Malta
•Spain

🚨Demanding an immediate suspension of COVID-19 modified mRNA “vaccines” aka
DANGEROUS GENE THERAPIES pic.twitter.com/Un4kegGgtL
— Alex🌺| Life Coach and Ethical Philosopher (@Luminousthght) December 22, 2024

# data[].attributes.attachment_link.metadata.attachment_props_source.data.text
🚨BREAKING NEWS: Dec. 17, 2024

🚨THREE MORE COUNTRIES JOIN NORTHGROUP

•Hungary
•Malta 
•Spain 

🚨Demanding an immediate suspension of COVID-19 modified mRNA “vaccines” aka
DANGEROUS GENE THERAPIES https://t.co/Un4kegGgtL

# data[].attributes.attachment_link.metadata.attachment_props_source.includes.users[].name
Alex🌺| Life Coach and Ethical Philosopher

# data[].attributes.attachment_link.metadata.attachment_props.original_text
🚨BREAKING NEWS: Dec. 17, 2024

🚨THREE MORE COUNTRIES JOIN NORTHGROUP

•Hungary
•Malta 
•Spain 

🚨Demanding an immediate suspension of COVID-19 modified mRNA “vaccines” aka
DANGEROUS GENE THERAPIES https://t.co/Un4kegGgtL

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🚨BREAKING NEWS: Dec. 17, 2024

🚨THREE MORE COUNTRIES JOIN NORTHGROUP

•Hungary
•Malta 
•Spain 

🚨Demanding an immediate suspension of COVID-19 modified mRNA “vaccines” aka
DANGEROUS GENE THERAPIES https://t.co/Un4kegGgtL

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Alex🌺| Life Coach and Ethical Philosopher

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Own Your Labs is an easy to use website for ordering your blood tests directly in the United States.

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Own Your Labs is an easy to use website for ordering your blood tests directly in the United States.

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Hello everyone - welcome to Own Your Labs. Own Your Labs is an easy to use website for ordering your blood tests directly in the United States. For more a more [...]

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   Pfizer/BioNTech's COVID-19 modRNA Vaccines: Dangerous Genetic Mechanism of Action Released before Sufficient Preclinical Testing

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   Pfizer/BioNTech's COVID-19 modRNA Vaccines: Dangerous Genetic Mechanism of Action Released before Sufficient Preclinical Testing

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https://www.jpands.org/jpands2904.htm

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https://publichealthpolicyjournal.com/biontech-rna-based-covid-19-injections-contain-large-amounts-of-residual-dna-including-an-sv40-promoter-enhancer-sequence/

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Menstrual Abnormalities Strongly Associated with Proximity to COVID-19 Vaccinated Individuals

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Menstrual Abnormalities Strongly Associated with Proximity to COVID-19 Vaccinated Individuals

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https://ijvtpr.com/index.php/IJVTPR/article/view/113

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https://www.vi-ta.org/

"The cries for help cannot be ignored. That is why we have created VI-TA, to offer support and resources for the Vaccine Injured." - Dr. Christina Parks

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Yes, they did use HIV to cause immunosuppression in the bioweapon COVID-19.

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Yes, they did use HIV to cause immunosuppression in the bioweapon COVID-19.

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Yes, they did use HIV to cause immunosuppression in the bioweapon COVID-19. pic.twitter.com/DMZxSUvL1c
— Brian Tyson, MD 🇺🇸 (@btysonmd) November 30, 2024

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The Government Cartel paid billions to Walgreens and CVS not to fill Ivermectin - the question is why

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Drug dealing, it seems, has always been a lucrative business, especially when the drug lord of your cartel is the federal government. Why in the world would…

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The heartbreaking moment Professor Ian Brighthope breaks down in tears in front of thousands in Perth as he realises that 60 million deadly vaccines have been administered to innocent Australians now causing death and turbo cancer.

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❗️The heartbreaking moment Professor Ian Brighthope breaks down in tears in front of thousands in Perth as he realises that 60 million deadly vaccines have been administered to innocent Australians now causing death and turbo cancer.

😢This is huge. 🇦🇺Australia is rising!… pic.twitter.com/YFXvAUziFd
— jamiemcintyre (@jamiemcintyre21) November 29, 2024

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Evidence of DNA contamination in the COVID jabs, led to the Port Hedland Council in WA, AU SUSPENDING ALL MRNA VACCINES. 

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Evidence of DNA contamination in the COVID jabs, led to the Port Hedland Council in WA, AU SUSPENDING ALL MRNA VACCINES. 

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A new motion brought by the Port Hedland Council, in Western Australia, gets a 5-2 majority vote to "Call for an immediate suspension of the Pfizer and Moderna COVID-19 products".

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NEW. HISTORIC MOMENT IN AUSTRALIA. The action that results from this could end up sweeping the World

A new motion brought by the Port Hedland Council, in Western Australia, gets a 5-2 majority vote to "Call for an immediate suspension of the Pfizer and Moderna COVID-19… pic.twitter.com/Wnq4yh5fRG
— Humanspective (@Humanspective) October 12, 2024

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Big Pharma Still Won’t Come Clean About The Covid Shot’s Deadly Side Effects

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Big Pharma Still Won’t Come Clean About The Covid Shot’s Deadly Side Effects

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https://www.aussie17.com/p/malaysians-launch-class-action-lawsuit

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Transplacental transmission of the COVID-19 vaccine messenger RNA: evidence from placental, maternal, and cord blood analyses postvaccination

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https://x.com/drtrozzi/status/1741201364443881713?s=12

Dr. Trozzi Alert | There’s DNA in the RNA Shots. Lots! My 15 Minute video explaining very concerning new revelations and implications.

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Dr Trozzi Alert | There’s DNA in the RNA Shots. Lots! My 15 Minute video explaining very concerning new revelations and implications. #mRNA pic.twitter.com/XmTTxXvy8q
— Dr Mark Trozzi MD (@DrTrozzi) December 30, 2023

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DMSO is a Miraculous Therapy for Chronic Pain and Musculoskeletal Injuries

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DMSO is a Miraculous Therapy for Chronic Pain and Musculoskeletal Injuries

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https://www.midwesterndoctor.com/p/dmso-is-a-miraculous-therapy-for

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https://www.midwesterndoctor.com/p/how-dmso-cures-eye-ear-nose-throat

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COVID-19 Vaccines: A Risk Factor for Cerebral Thrombotic Syndromes

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COVID-19 Vaccines: A Risk Factor for Cerebral Thrombotic Syndromes

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https://ijirms.in/index.php/ijirms/article/view/1982

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In Defense of the Vaccine Injured - Cody's Law

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Help Us Push For Life-Saving Help Now! Intl - In Defense of the Vaccine Injured - Cody’s Law

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Help Us Push For Life-Saving Help Now! The Vaccine Injured Have Been In The Shadows Long Enough, Sign Our Petition to Demand Change Now And Get Them The Help Needed! Worldwide, our injured were coerced and manipulated into thinking they were doing the right thing by taking untested, unproven COVID shots. Every country promoted the […]

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https://www.semanticscholar.org/paper/Can-new-onset-psychosis-occur-after-mRNA-based-A-Reinfeld-C%C3%A1ceda/9c320c193b91e4816c21ab6e611f9ed0626274dc

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July 31, 2020 @RepBillFoster questions @NIH Dr. Fauci re: COVID-19 mRNA bioweapon injection R&D. In 2013 @BarackObama gave $25M via @DARPA to startup @moderna_tx to develop mRNA injections, followed by $125M to @BARDA in 2015.

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💸Obama Funded Warp Speed💉

July 31, 2020 @RepBillFoster questions @NIH Dr. Fauci re: COVID-19 mRNA bioweapon injection R&D. In 2013 @BarackObama gave $25M via @DARPA to startup @moderna_tx to develop mRNA injections, followed by $125M to @BARDA in 2015.https://t.co/T5whtqUOrZ pic.twitter.com/3xqYEuKACL
— Not Op Cue (@NotOpCue) August 24, 2024

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Obama Re-Authorized Propaganda 2013  
  📰🗞️📺🌐📰🗞️📺🌐📰🗞️📺🌐

July 2, 2013 the Smith-Mundt Modernization Act of 2012 went into effect when @BarackObama incorporated it into the NDAA 2013, effectively enabling propaganda on Americans. 

H.R.4310 - National Defense… https://t.co/3xVJfOntr1 https://t.co/6PGEvUInz9

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Obama Re-Authorized Propaganda 2013  
  📰🗞️📺🌐📰🗞️📺🌐📰🗞️📺🌐

July 2, 2013 the Smith-Mundt Modernization Act of 2012 went into effect when @BarackObama incorporated it into the NDAA 2013, effectively enabling propaganda on Americans. 

H.R.4310 - National Defense… https://t.co/3xVJfOntr1 https://t.co/6PGEvUInz9

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💸Obama Funded Warp Speed💉

July 31, 2020 @RepBillFoster questions @NIH Dr. Fauci re: COVID-19 mRNA bioweapon injection R&D. In 2013 @BarackObama gave $25M via @DARPA to startup @moderna_tx to develop mRNA injections, followed by $125M to @BARDA in 2015.
https://t.co/T5whtqUOrZ https://t.co/9vmUN4MOlI https://t.co/3xqYEuKACL

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Obama Re-Authorized Propaganda 2013
📰🗞️📺🌐📰🗞️📺🌐📰🗞️📺🌐

July 2, 2013 the Smith-Mundt Modernization Act of 2012 went into effect when @BarackObama incorporated it into the NDAA 2013, effectively enabling propaganda on Americans.

H.R.4310 - National Defense… pic.twitter.com/6PGEvUInz9
— Not Op Cue (@NotOpCue) November 12, 2024

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Obama Re-Authorized Propaganda 2013  
  📰🗞️📺🌐📰🗞️📺🌐📰🗞️📺🌐

July 2, 2013 the Smith-Mundt Modernization Act of 2012 went into effect when @BarackObama incorporated it into the NDAA 2013, effectively enabling propaganda on Americans. 

H.R.4310 - National Defense… https://t.co/3xVJfOntr1 https://t.co/6PGEvUInz9

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💸Obama Funded Warp Speed💉

July 31, 2020 @RepBillFoster questions @NIH Dr. Fauci re: COVID-19 mRNA bioweapon injection R&D. In 2013 @BarackObama gave $25M via @DARPA to startup @moderna_tx to develop mRNA injections, followed by $125M to @BARDA in 2015.
https://t.co/T5whtqUOrZ https://t.co/9vmUN4MOlI https://t.co/3xqYEuKACL

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Obama Re-Authorized Propaganda 2013  
  📰🗞️📺🌐📰🗞️📺🌐📰🗞️📺🌐

July 2, 2013 the Smith-Mundt Modernization Act of 2012 went into effect when @BarackObama incorporated it into the NDAA 2013, effectively enabling propaganda on Americans. 

H.R.4310 - National Defense… https://t.co/3xVJfOntr1 https://t.co/6PGEvUInz9

# data[].attributes.attachment_link.metadata.attachment_props.text
Obama Re-Authorized Propaganda 2013  
  📰🗞️📺🌐📰🗞️📺🌐📰🗞️📺🌐

July 2, 2013 the Smith-Mundt Modernization Act of 2012 went into effect when @BarackObama incorporated it into the NDAA 2013, effectively enabling propaganda on Americans. 

H.R.4310 - National Defense… https://t.co/3xVJfOntr1 https://t.co/6PGEvUInz9

# data[].attributes.attachment_link.metadata.attachment_props.referenced_tweets[].text
💸Obama Funded Warp Speed💉

July 31, 2020 @RepBillFoster questions @NIH Dr. Fauci re: COVID-19 mRNA bioweapon injection R&D. In 2013 @BarackObama gave $25M via @DARPA to startup @moderna_tx to develop mRNA injections, followed by $125M to @BARDA in 2015.
https://t.co/T5whtqUOrZ https://t.co/9vmUN4MOlI https://t.co/3xqYEuKACL

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National Citizen's Inquiry - Canada's Response To Covid-19

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NCI Live - National Citizen’s Inquiry - Canada’s Response To Covid-19

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Upcoming and past live events with the volunteers of the National Citizens Inquiry. Check here often for updates, and follow NCI !

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https://publichealthpolicyjournal.com/a-systematic-review-of-autopsy-findings-in-deaths-after-covid-19-vaccination/

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The EVIDENCE is clear. The mRNA VACCINES were developed by DARPA & DOD long ago, at least as early as 2012 according to this DARPA document linked above and pictured below.

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SEARCH: DARPA ADEPT P3https://t.co/vovc4DApjP

The EVIDENCE is clear. The mRNA VACCINES were developed by DARPA & DOD long ago, at least as early as 2012 according to this DARPA document linked above and pictured below. pic.twitter.com/URvGHYv7tX
— James Thorp MD (@jathorpmfm) November 21, 2024

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Ever wondered why governments & media relentlessly reported every COVID-19 death? It wasn't just to inform or scare us- but, also to shape perceptions in the long-term. Were all those deaths truly caused by the virus? Let's dive into the C19 Vaccine injuries.

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1🧵Ever wondered why governments & media relentlessly reported every COVID-19 death? It wasn't just to inform or scare us- but, also to shape perceptions in the long-term. Were all those deaths truly caused by the virus? Let's dive into the C19 Vaccine injuries. pic.twitter.com/IQYrq7AEzO
— Destiny Rezendes (@dezzie_rezzie) January 10, 2024

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The excess all-cause mortality that we have quantified (31 million globally during 2020-2022) is only the most easily recognized node in a large network of pain and destruction

31 million

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The excess all-cause mortality that we have quantified (31 million globally during 2020-2022)
is only the most easily recognized node in a large network of pain and destruction
31 million: https://t.co/9jKuN0Egdm pic.twitter.com/0XkAID2ULJ
— Denis Rancourt (@denisrancourt) October 6, 2024

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Prof. Angus Dalgleish was on Sky News Australia: About the UK Chief Scientific Officer Chris Whitty, he said "he's a total moron..these were not vaccines, these were horrible gene therapies that could actually intergrate into your genome, and this is one of the reasons we are seeing this horrendous rise in turbo-cancers. I'm terrified what they've done to our children..."

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@AusFireAlliance A better quality version for you. 
Credit: @SkyNewsAust @rowandean @RitaPanahi https://t.co/rH9ocLlltX

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@AusFireAlliance A better quality version for you. 
Credit: @SkyNewsAust @rowandean @RitaPanahi https://t.co/rH9ocLlltX

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Esteemed Professor of Oncology Angus Dalgleish, interviewed today on SkyNews Australia.

Professor Dalgleish talks to the Oncogenic risks of the mandated Covid products, directly calling into question the Cancer initiatives that have been fostered in Victoria for the firefighting… https://t.co/WVFxKFQrJU https://t.co/MLyTKFFqGY

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A better quality version for you.
Credit: @SkyNewsAust @rowandean @RitaPanahi pic.twitter.com/rH9ocLlltX
— Jikkyleaks 🐭 (@Jikkyleaks) November 24, 2024

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@AusFireAlliance A better quality version for you. 
Credit: @SkyNewsAust @rowandean @RitaPanahi https://t.co/rH9ocLlltX

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Esteemed Professor of Oncology Angus Dalgleish, interviewed today on SkyNews Australia.

Professor Dalgleish talks to the Oncogenic risks of the mandated Covid products, directly calling into question the Cancer initiatives that have been fostered in Victoria for the firefighting… https://t.co/WVFxKFQrJU https://t.co/MLyTKFFqGY

# data[].attributes.attachment_link.metadata.attachment_props.original_text
@AusFireAlliance A better quality version for you. 
Credit: @SkyNewsAust @rowandean @RitaPanahi https://t.co/rH9ocLlltX

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@AusFireAlliance A better quality version for you. 
Credit: @SkyNewsAust @rowandean @RitaPanahi https://t.co/rH9ocLlltX

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Esteemed Professor of Oncology Angus Dalgleish, interviewed today on SkyNews Australia.

Professor Dalgleish talks to the Oncogenic risks of the mandated Covid products, directly calling into question the Cancer initiatives that have been fostered in Victoria for the firefighting… https://t.co/WVFxKFQrJU https://t.co/MLyTKFFqGY

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Say Goodbye to strange pain, inflammation, stubborn weight, fatigue and low self-confidence. Say YES to vitality and personal control of health.

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Confirmation of the presence of vaccine DNA in the Pfizer anti-COVID-19 vaccine

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Confirmation of the presence of vaccine DNA in the Pfizer anti-COVID-19 vaccine

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https://hal.science/hal-04778576v1

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https://www.strokebreakthrough.com/

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Biden Admin spent 1 Billion on Propaganda to push the shots

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Biden Admin spent 1 Billion on Propaganda to push the shots

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The Most Devastating Report So Far ⋆ Brownstone Institute

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The House report on HHS Covid propaganda is devastating. Biden administration pushed falsehoods about Covid vaccines, boosters, and masks.

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“Get to the root cause of your low mood, fatigue, weight gain, & rapid aging with at-home lab testing...”

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Dr Ana Mihalcea PROVES with Dark Field Blood Microscopy that NON-vaccinated are being transfected with mRNA NANOTECH: Shows EDTA & vitamin C stop self assembling Nanotech in vivo…other solutions given

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IMO, the SERIOUS ISSUE OF NON-VACCINATED being TRANSFECTED WITH mRNA NANOTECH TRUMPS the STUDY “showing >90% of UNINFECTED adults with pre-existing antibody reactivity against SARS-CoV-2”

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Idaho Health Board First in U.S. to Defy CDC and FDA by Removing COVID Vaccines From Clinics

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Idaho’s Southwest District Health will no longer offer COVID-19 vaccines after its board voted 4-3 last week to pull the shots from the 30 locations where it provides healthcare services.

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Shedding of Covid mRNA Vaccine Products - A Review Of The Scientific, Regulatory, and Clinical Evidence

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In collaboration with A Midwestern Doctor, we compiled all of the scientific, regulatory, and clinical evidence that mRNA vaccine recipients can cause symptoms in others via shedding of spike protein.

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COVID-19 Menstrual & Breast Milk Disruptions, Miscarriages, Infertility, Shedding, DNA Contamination | Sunfellow Notes

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Must Watch & Share: COVID-19 VACCINE SHEDDING IS REAL! (11/01/23 - FLCCC Weekly Update)

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What is “shedding”? And what are the implications for our health? Host Betsy Ashton was joined by Dr. Pierre Kory, Dr. Paul Marik and Scott Marsland, FNP-C for this important discussion centered aroun

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On Wall Street when you have an investment thesis that’s contrarian you need to show your work. 

Over the last 2 plus years we have assembled a body of work that presents our analyst mosaic that the Covid mRNA vaccines have caused excess deaths disabilities & injuries. 
Our… https://t.co/cEkQw1sAGz

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On Wall Street when you have an investment thesis that’s contrarian you need to show your work. 

Over the last 2 plus years we have assembled a body of work that presents our analyst mosaic that the Covid mRNA vaccines have caused excess deaths disabilities & injuries. 
Our… https://t.co/cEkQw1sAGz https://t.co/bQpv5MEFJ3

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On Wall Street when you have an investment thesis that’s contrarian you need to show your work.

Over the last 2 plus years we have assembled a body of work that presents our analyst mosaic that the Covid mRNA vaccines have caused excess deaths disabilities & injuries.
Our… pic.twitter.com/bQpv5MEFJ3
— Edward Dowd (@DowdEdward) September 12, 2024

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On Wall Street when you have an investment thesis that’s contrarian you need to show your work. 

Over the last 2 plus years we have assembled a body of work that presents our analyst mosaic that the Covid mRNA vaccines have caused excess deaths disabilities & injuries. 
Our… https://t.co/cEkQw1sAGz https://t.co/bQpv5MEFJ3

# data[].attributes.attachment_link.metadata.attachment_props.original_text
On Wall Street when you have an investment thesis that’s contrarian you need to show your work. 

Over the last 2 plus years we have assembled a body of work that presents our analyst mosaic that the Covid mRNA vaccines have caused excess deaths disabilities & injuries. 
Our… https://t.co/cEkQw1sAGz https://t.co/bQpv5MEFJ3

# data[].attributes.attachment_link.metadata.attachment_props.text
On Wall Street when you have an investment thesis that’s contrarian you need to show your work. 

Over the last 2 plus years we have assembled a body of work that presents our analyst mosaic that the Covid mRNA vaccines have caused excess deaths disabilities & injuries. 
Our… https://t.co/cEkQw1sAGz

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Dr David Cartland BMedSci MBChB MRCGP (2014)

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32 Vaccine documentaries

(links updated 17April22)

1. Vaccination – The Silent Epidemic –https://t.co/YdP7VtxMa5

2. The Greater Good – https://t.co/AU3w7f2rRK

3. Shots In The Dark – https://t.co/EW9zpi54kx

4. Vaccination The Hidden Truth – https://t.co/JGYtaQ8Y9f

5.…
— Dr David Cartland BMedSci MBChB MRCGP (2014) (@CartlandDavid) September 11, 2024

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Then life insurance industry data emerged showing historically unprecedented rises in death claims being paid out amongst the healthiest sectors of society temporally associated with the proliferation of Covid mRNA vaccine mandates within schools, corporations, universities, health care institutions, federal contractors etc. Most telling of the deathly impact of mandates was the fact that the largest increases among the sudden, rapid rises in excess deaths occurred among employed white collar workers.

The reality is that these data are still ignored by media and public health agencies across the world. Even more worrying are the more recent reports finding universal contamination of every studied vaccine vial with large magnitude, excess levels of DNA fragments and DNA plasmids. Then the discovery that the DNA plasmids used in the manufacturing process contained genetic sequences that both promote DNA integration into the human genome as well as promote the development of cancer.

It truly is unimaginable that we now must consider the risks (and reality) of "shedding" of the vaccine products from the vaccinated to the unvaccinated. This now has implications for nearly every human being walking the earth, vaccinated or unvaccinated (including me).

This series will explore the regulatory, scientific, epidemiological, and clinical data indicating that shedding is occurring. The health of who knows how many is now being threatened, with the extent of the risks likely both highly variable and difficult to predict, both in the short term and long term. That is unless we start to seriously study the phenomenon further. So, let's review what is known.

Within 3 months of the rollout of the global Covid mRNA vaccination campaign, I was consulted by two different unvaccinated women in their late 30's and early 40's respectively, who reported that they were suffering acute menstrual abnormalities in the days following close exposure to a recently vaccinated practitioner (one visited a massage therapist and another an acupuncturist). Both had a history of highly regular, uncomplicated menstrual cycles over decades.

Since that time, at least twenty other unvaccinated and vaccinated people, both men and women, have reported to me compelling histories of typical post-mRNA vaccine adverse effects subsequent to close exposure to vaccinated family members, contacts, or friends.

This is further complicated by the fact that even if it were occurring frequently, the vast majority of people suddenly developing typical vaccine side effects symptoms after exposure to a vaccinated person would never think to relate it to exposure to shed vaccine products. It is my belief that very few people in the general public are aware of the possibility it could occur. You know, because the regulators have assured the country that mRNA technology is "safe and effective."

However, my general sense is that it occurs largely in people who have increased physiologic sensitivity to environmental exposures, toxins, or pharmaceuticals and that it is generally transmitted by someone recently vaccinated or someone who is producing a lot of spike protein. Note that is my "general sense." More studies are required to fully understand both the frequency of and physiologic impacts from such events.

My ignorance as to the frequency of symptomatic shedding events is due to the fact that the concept of transmitting spike proteins (or lipid nanoparticles) from a Covid mRNA vaccinated person to another is one of the least studied and published-on aspect of the mRNA vaccine technology.

As a physician committed to education, I (finally) decided to respond to the void of information around shedding with this series of deeply researched posts. If you appreciate the effort, please consider supporting my commitment to continuing this Substack with a paid subscription (I have been debating whether to give it up due to too many competing demands of my time - help me make that decision :).

Anyway, I believe that by the end of this series on the science, epidemiology, and clinical observations of shedding, you will be convinced that it can and does occur.
"The release of viral or bacterial gene therapy products from the patient by any or all of the following routes: feces (feces); secretions (urine, saliva, nasopharyngeal fluids, etc.); or through the skin (pustules, lesions, sores)."
They forgot to mention "exhaled breath." More on that later. The "products" they refer to that can be transmitted from a Covid vaccinated person to another include not only the genetically programmed spike protein product, but also the lipid nanoparticle (LNP) containing the mRNA that is in the injections as well as naked mRNA that can be released from the LNP. Even more worrying is the recent shocking discovery that every single Moderna and Pfizer vaccine vial is contaminated with high levels of DNA plasmids potentially capable of integrating into the human genome. Contemplating that last one is disturbing, the implications of which we will not know for some time.

First off, let's be clear that the Covid mRNA and DNA vaccines are gene therapy medicinal products (GMTPs or GTP's) as stated in the FDA's 2015 document on Gene Product Shedding Studies.

"Gene therapy products are all products that mediate their effects by transcription and/or translation of transferred genetic material and/or by integrating into the host genome and that are administered as nucleic acids, viruses, or genetically engineered microorganisms.

Ok, now that we know what a gene therapy product is and that the Covid mRNA injection is actually a form of gene therapy (marketed to the public as a "vaccine"), what does that have to do with "shedding?" Again from the FDA document regarding the evaluation of the safety of gene therapy products, they emphasize the importance of studying shedding:

Shedding is distinct from biodistribution because the latter describes how a product is spread within the patient's body from the site of administration while the former describes how it is excreted or released from the patient's body. Shedding raises the possibility of transmission of virus or bacteria based gene therapy products (VBGT) from treated to untreated individuals (e.g., close contacts and health care professionals). This guidance represents FDA's current thinking on how and when shedding data should be collected for VBGT and oncolytic products during preclinical and clinical development and how shedding data can be used to assess the potential for transmission to untreated individuals.

So, with these findings in mind, it may be no wonder why the FDA insists on shedding studies:

Further on in the document, the FDA emphasizes the importance of doing human shedding studies and not just relying on animal studies:

To inform the design of human shedding studies, shedding data may be collected in animals following administration of the VBGT or oncolytic product. These data can help estimate the likelihood and potential shedding profile in humans, particularly when there is concern about transmission to untreated individuals. However, such data cannot substitute for human shedding studies for several reasons.

But again, no studies testing whether excretion of mRNA-containing LNPs, modified spike-encoding mRNA, or spike produced by vaccinated people have been done. Well, I shouldn't say none, because in this paper the author cites a Pfizer document obtained by FOIA which apparently revealed that shedding was studied in the urine and feces of intra-muscular injected rats. Unfortunately, t hat document is no longer at the website referenced.

the mRNA vaccines are gene therapy products

Gene therapy products require shedding studies in both animals and humans

Gene therapy product shedding raises the possibility of transmission from treated to untreated individuals

To summarize from the above, the FDA's position is that:

Note that much of the rest of this series of posts on shedding is guided by a masterful comprehensive review of the topic of gene therapy product shedding by independent researcher (by definition) Helene Banoun in Infectious Diseases Research. Hers is one of the only papers I could find that attempted to meticulously explore what is known about shedding of the mRNA gene therapy vaccines.

As already stated, an important point Banoun makes is:

There was no regulation of mRNA clinical trials prior to RNA vaccines, yet there is strict regulation of gene therapy products. It is difficult to justify that mRNA vaccines are not considered in the same way as gene therapies regarding this regulation; indeed the only difference is that they are (historically ) supposed to protect against a disease and not cure it. Gene therapies are intended for a small number of people in poor health, whereas vaccines are used on a large scale on healthy people: it would therefore be wise to apply stricter rules to them.

She further points out another omission of the regulatory process:

Any experiment involving the deliberate transfer of a nucleic acid to a human must be preceded by Institutional Biosafety Committee approval (document on the regulatory standards is here), but approval was not given because of the emergency clearance given to mRNA vaccines.

Therefore, according to both the American and European agencies, mRNA vaccines are gene therapy products and should have been subjected to excretion studies of all secreted fluids (urine, exhaled droplets, saliva, sputum, nasopharyngeal fluids, semen, breast milk, feces, and sweat). Again, these studies were not done for mRNA vaccines nor for the DNA adenovirus vaccine (J&J).

So, where are the clinical human shedding studies? Well, I just learned of one that is about to be published (next ten days?) where the research team exposed a population of unvaccinated women to vaccinated individuals and their assessment outcome was the development of menstrual abnormalities. I know the results but want to respect the research teams right to present their original work. They have promised to share their manuscript with me and Paul Marik as soon as the peer-review and acceptance process is complete. I have no idea what journal they submitted to but I can be highly confident it is not the New England Journal of Medicine.

The entire reason why I did a "deep dive" into shedding science is because shedding was not studied when it absolutely should have been and I believe with near certainty that it occurs. Note my use of "near certain" is only to seem objective but it really is too late for that - both my partner Scott and I have diagnosed and successfully treated a number of shedding "victims."

The lack of shedding studies prior to the mRNA rollout was, in my opinion, an insanely reckless and irresponsible omission (or willfully criminal, take your pick). As an evolving expert in the evaluation and treatment of Covid mRNA vaccine injury syndromes, I and others have identified the spike protein as the main component responsible for not only the pathogenicity of Covid but also of the vaccines, with this review paper proposing a new field named "spikeopathy" (study of the disease processes triggered by the spike protein).

If vaccine transcribed spike protein can be transmitted in sufficient quantity from vaccinated folks to unvaccinated ones, it stands to reason that adverse effects of the vaccine can develop in some unvaccinated people who came into contact (or close proximity) with vaccinated people. How did they get away with not studying this possibility?

An easy answer is they were doing science at "warp speed." The more uncomfortable answer is that the "vaccines", although meeting the definition of a gene therapy product, were actually not even legally considered a medical product at all and thus did not require a diverse range of safety studies (like on genotoxicity, reproductive risks, excretion potential etc). What? Why? How?

The reality is that the Covid vaccines, as a result of successive federal legislative actions which evolved over decades, was legally categorized as a "countermeasure" under a "public health emergency." Such "countermeasures" require no specific regulatory approval process prior to dissemination. All a countermeasure needs is the recommendation of the Secretary of Health and Human Services that "it may be effective."

This is the conclusion derived from the legal investigatory work of various independent and legal experts and researchers like Catherine Watts, Todd Callender, and Sasha Latypova. If interested in learning more, I would watch this lecture by Sasha Latypova (scroll down the page to find her lecture). As they have uncovered, "countermeasures" (even gene therapy ones) do not legally require studies of excretion potential, bio-distribution, pharmacokinetics, genotoxicity, insertional mutagenesis etc.

They don't even require FDA regulated clinical trials of efficacy or safety.

So why did Pfizer and Moderna even do the efficacy trials? Latypova maintains that they did this not only to satisfy the public's confidence to increase vaccine uptake, but also to "fool" the public into thinking these vaccines were medical products subject to standard (albeit accelerated) pharmaceutical product regulatory processes.

This obscured the reality that they were instead classified as military "countermeasures" against a perceived (if not actual) bioweapon. To wit, the COO of Operation Warp Speed was a General from the Department of Defense (DOD) and the vaccine manufacturers were under contract with the DOD to produce the countermeasure, sometimes referred to as a "demonstration (demo)" and/or a "prototype" in numerous legal documents they uncovered.

Anyway, as a result of this lack of a legal requirement to fully study these products in a public health emergency, the list and types of studies that should have been conducted (but were not) is long. Researchers and clinicians have been screaming about this since they were rolled out. These cries were met with a deafening silence by governmental health agencies across the world.

I know, it is a lot to take in.

But the latest "word on the street" is that the finance and insurance industries may finally be waking up to this fraud and its devastating impacts on U.S disability and death rates. Knowledge of these society-wide impacts largely results from the work of two different research teams led by former Blackrock portfolio manager Ed Dowd and insurance industry consultant Josh Stirling).

This article describes the reasons why Pfizer and Moderna stock are crashing of late. Put more succinctly, from what I hear it is due to the hedge fund guys shorting their stock. I believe Pfizer is in even deeper trouble now that this "forensic" paper just got published finding that they hid vaccine trial deaths which obscured a 3.7 fold increased risk of cardiac death in the vaccinated arm of their trial.

Links to all the other (already active) posts in this series is after the subscribe button below.

P.S. I just want to say thanks to all my subscribers, especially the paid ones! Your financial support is greatly appreciated as it allows me to devote what is often large amount of time I spend researching and writing my posts, so again, thanks. - Pierre

"Shedding" Part 1- Shedding of Covid mRNA Vaccine Components and Products From The Vaccinated to the Unvaccinated - Part 1

- The Bio-Distribution and Excretion Potential of Covid mRNA Vaccine Products

- Can You Absorb Lipid Nanoparticles From Being Exposed To a Vaccinated Person?

- Evidence of Placental and Breast Milk Transmission of Covid mRNA Vaccine Components

"Shedding" Part 5 - Evidence of Shedding Causing Illness In Others

"Shedding Part 6- Clinical Case Notes Describing Shedding Phenomena Among Leading Edge Clinic Patients

"Shedding" Part 7 - Shedding Via Sexual Intercourse - Clinical Reports

"Shedding" Part 8 - A Deluge of Clinic Reports Pour In

"Shedding" Part 9 - More and More Clinical Case Descriptions of Shedding Pour In

P.P.S - Proud to report that my book is gaining Best Seller status on Amazon in several countries and is climbing up the U.S Amazon rankings... Link:

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"Shedding" of Covid mRNA Vaccine Components and Products From The Vaccinated to the Unvaccinated - Part 1

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It's happening. The manufacturers and regulators knew it was a risk, yet, like numerous aspects of the Covid vaccine mRNA technology, did not test for excretion potential of spike proteins or LNP's.

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Humanity United Now - Ana Maria Mihalcea, MD, PhD 8.32K followers

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VAERS coverup of COVID19 bioweapon mortality -Conversation with Albert Benavides -EP 31

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In this episode, I speak with VAERS expert Albert Benavides about the ongoing VAERS data fraud. He shows evidence of how the system is being scrubbed to cover up true injury and mortality rates. Alber

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A new peer-reviewed study published in the journal Andrology on June 17 vindicates another dark suspicion about COVID-19 vaccines: They harm male fertility. Specifically, researchers find declining sperm counts for up to five months after the second dose of Pfizer's mRNA COVID-19 jab.

Previously, any legitimate questions about COVID-19 vaccination affecting fertility were dismissed using the perverse rhetoric of "there's no evidence" (it's dependent upon the advocates of a universally distributed medical product to prove it's safe, not the other way around). Then, there was a published study that seemingly disproved any male fertility concerns.

"We now have evidence that should reassure you that the risk of immunization compromising your sperm count is extremely low," Dr. David Cohen, a reproduction expert, told CNN.

"Because the vaccines contain mRNA and not the live virus, it is unlikely that the vaccine would affect sperm parameters," stated study author Dr. Ranjith Ramasamy, director of the Reproductive Urology Fellowship program at the University of Miami.

After the publication of the study and positive support from the scientific community, all male fertility concerns were brushed aside. Anyone who dared to question the parameters of the study or the longer-term effects was relegated to a conspiracy theorist. As someone who generally doesn't like to engage in speculation, I wasn't one of these people-but I vividly recall it happening.

There was one severe limitation of the study: It only looked at sperm counts before the first dose and 70 days after the second. What happens after two months remained a mystery, but a mystery not worth worrying about, we were told.

The new study published in Andrology tested beyond 70 days and tested sperm counts from men who donated sperm to three fertility clinics in Israel. The study had four phases: a pre-vaccination baseline control, and a short-term (15-45 days), intermediate (75-120 days), and long-term (>150 days) test.

In the first phase (15-45 days), no significant change in sperm concentration or motility was found.

However, the intermediate evaluation (75-120 days) showed a temporary 15.4 percent sperm concentration decrease, which led to a total motile count (TMC) reduction of 22.1 percent compared to the pre-vaccination baseline control. The study authors concluded that the immune response induced by the Pfizer vaccine "is a reasonable cause for transient semen concentration and TMC decline."

This study isn't without its limitations. There was no control group of unvaccinated sperm donors to compare to. Moreover, only relative reduction rates were given rather than absolute sperm counts. If the broader data paints an even darker picture, it's possible it was obscured given the tremendous amount of public and institutional pressure to support the unchallengeable holy biotechnology (see the backlash Dr. Tracy Beth Hoeg and colleagues faced for publishing the vaccine myocarditis studies).

The biggest unanswered question from this study is the reproductive side effects associated with a booster shot. Study participants were given a third dose, but data collection ended after the second shot. Moreover, this data is only for the Pfizer vaccine. As we've seen with myocarditis, the Moderna vaccine has severalfold (approximately 3 to 5 times) higher rates of myocarditis compared to Pfizer. If the differential vaccine damage for myocarditis in any way aligns with sperm count impairment, this would be a medical disaster.

Vaccine fanatics have always dismissed concerns as "conspiracy theory." That vaccines are wildly ineffective at preventing transmission was once a conspiracy theory. Former New York Times reporter Alex Berenson was kicked off Twitter for making this claim, alongside other "misinformation."

Robust evidence showing vaccines cause an unacceptably high rate of myocarditis in men has also been bizarrely challenged, ignored, and distorted (see Dr. Sanjay Gupta on The Joe Rogan Experience).

Being concerned with "long-term side effects" was treated like speculating whether the Earth is flat.

Vaccine advocates made the grave mistake of overconfidently assuming the unknowns were completely benign, and any consideration otherwise was blasphemous.

Science isn't religious scripture-it's an ever-evolving process. With the new data in, responsible scientists must acknowledge this risk and compare it with the potential benefits of vaccination (against severe disease and death). And accordingly, the one-size-fits-all "everyone 5 and up should get boosted" propaganda campaign must be scrapped in favor of age-specific, individualized decision-making.

A 30-year-old male looking to start a family may be reasonably discouraged from getting vaccinated (or now getting a booster) given the new data; meanwhile, a frail 75-year-old man with multiple comorbidities would much rather be protected from the potentially lethal consequences of COVID-19.

The question is, will the public health authorities and top epidemiologists re-evaluate their universal vaccine advisory and honestly discuss the risks?

If not, I may contend "science is dead" with Nietzschean zeal.
Views expressed in this article are opinions of the author and do not necessarily reflect the views of The Epoch Times.

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Pfizer Vaccine Impairs Sperm Count-Conspiracy Theorists Were Right

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A new peer-reviewed study published in the journal Andrology on June 17 vindicates another dark suspicion about COVID-19 vaccines: They harm male fertility. Specifically, researchers find declining sperm counts for up to five months after the second dose of Pfizer's mRNA COVID-19 jab.

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After the first of two weeks to flatten the curve of COVID-19 cases, President Donald Trump said, "We cannot let the cure be worse than the problem itself." He was right, yet that ill fate prevailed in the U.S., Canada, and much of the world.

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An important paper released July 19 by three Canadian academics Denis Rancourt, Joseph Hickey, and Christian Linard in Correlation Research proved this when looking at how many more people died than usual (excess mortality) in 125 countries with a total of 2.7 billion people.

The researchers found "essentially no excess mortality, in any country, prior to the 11 March 2020 WHO declaration of a pandemic." Yet, deaths spiked significantly in 26 countries before the end of the month, including the U.S. and Canada.

Elsewhere, a small rise occurred in 11 countries and none happened in 88 others. Was this a pandemic or a damned panic?

Although a virus doesn't stop at a political border, patterns of excess death varied significantly, even between adjacent countries. The only continuity was higher death rates among the old and poor.

Many countries had "various large peaks and periods of excess-all cause mortality" from 2020 to 2023, the paper explains, ones that defy seasonal patterns and what a pandemic alone would suggest.

Such findings were "incompatible with a pandemic viral respiratory disease as a primary cause of death," the researchers concluded. In other words, the excess deaths were not caused by the virus.

If a virus didn't do it, what did? The researchers laid out three plausible mechanisms, stated here verbatim:

"Biological (including psychological) stress from mandates such as lockdowns and associated socio-economic structural changes. Non-COVID-19-vaccine medical interventions such as mechanical ventilators and drugs (including denial of treatment with antibiotics). COVID-19 vaccine injection rollouts, including repeated rollouts on the same populations."

That's right. Governments propagandized and coerced populations around the world into taking shots that did more harm than good.

The researchers explained, "Many countries have no excess mortality until the vaccines are rolled out. Several countries show temporal associations between vaccine rollouts and peaks or increases in all-cause mortality."

Astonishingly, in other words, 16.9 million excess deaths worldwide were associated with COVID-19 vaccinations. Overall, the three years in view (2020-2022) saw 29.8 million excess deaths, a number more than 4.2 times what the WHO reported as COVID-19 deaths.

"Generally speaking, excess all-cause mortality... often persists to the end of 2022, and most often returns to small or near-zero values in 2023," the researchers found. "Nonetheless, there are some notable examples in which excess all-cause mortality is large in 2023, and many countries in which there is apparent moderate but sustained excess all-cause mortality into 2023."

These 32 countries of continued excess deaths at rates of 5% to 15% include Canada and the U.S. Why?

Of 76 countries with statistically reliable data, nine had virtually no excess mortality for more than one year into the pandemic. That's curious, too.

Among 93 countries with reliable data, researchers found a 0.38 per cent excess mortality rate. India, which was excluded from the study, had just 0.26 per cent excess deaths, while Greenland had none.

Questions remain, but too few for the researchers to reach a stunning conclusion:

"We are compelled to state that the public health establishment and its agents fundamentally caused all the excess mortality in the Covid period, via assaults on populations, harmful medical interventions and COVID-19 vaccine rollouts."
- Lee Harding is a Research Fellow at the Frontier Centre for the Public Policy

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OPINION: COVID cure was worse than the disease: researchers

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After the first of two weeks to flatten COVID, President Donald Trump said, "We cannot let the cure be worse than the problem itself."