Scientists have known since December 2020 that the vaccines not only do not protect against the transmission of Covid-19 or reduce the severity of it, but actually make the vaccine recipients subject to more serious cases of the disease.
Informed consent disclosure to vaccine trial subjects of risk of COVID‐19 vaccines worsening clinical disease
COVID‐19 vaccines designed to elicit neutralising antibodies may sensitise vaccine recipients to more severe disease than if they were not vaccinated. Vaccines for SARS, MERS and RSV have never been approved, and the data generated in the development and testing of these vaccines suggest a serious mechanistic concern: that vaccines designed empirically using the traditional approach (consisting of the unmodified or minimally modified coronavirus viral spike to elicit neutralising antibodies), be they composed of protein, viral vector, DNA or RNA and irrespective of delivery method, may worsen COVID‐19 disease via antibody‐dependent enhancement (ADE). This risk is sufficiently obscured in clinical trial protocols and consent forms for ongoing COVID‐19 vaccine trials that adequate patient comprehension of this risk is unlikely to occur, obviating truly informed consent by subjects in these trials.
Conclusions drawn from the study and clinical implications
The specific and significant COVID‐19 risk of ADE should have been and should be prominently and independently disclosed to research subjects currently in vaccine trials, as well as those being recruited for the trials and future patients after vaccine approval, in order to meet the medical ethics standard of patient comprehension for informed consent.
This is exactly what is happening now and explains why so many incidents of the spread of the disease being reported among completely vaccinated populations. Covid-19 is increasingly becoming a disease of the vaccinated due to Antibody-Dependent Enhancement.
You can’t escape the experiment, so be the control group.
Your Vaccine Nazi friends and family may think they were sufficiently informed to consent to be vaccinated. They were not.
CONCLUSION
Given the strong evidence that ADE is a non‐theoretical and compelling risk for COVID‐19 vaccines and the “laundry list” nature of informed consents, disclosure of the specific risk of worsened COVID‐19 disease from vaccination calls for a specific, separate, informed consent form and demonstration of patient comprehension in order to meet medical ethics standards. The informed consent process for ongoing COVID‐19 vaccine trials does not appear to meet this standard.