Medical Paper “COVID-19 RNA Based Vaccines and the Risk of Prion Disease” – J. Bart Classen, MD*, Received 27 December 2020, Accepted 18 January 2021, Microbiology & Infectious Diseases,
“Abstract – Development of new vaccine technology has been plagued with problems in the past. The current RNA based SARS-CoV-2 vaccines were approved in the US using an emergency order without extensive long term safety testing. In this paper the Pfizer COVID-19 vaccine was evaluated for the potential to induce prion-based disease in vaccine recipients. The RNA sequence of the vaccine as well as the spike protein target interaction were analyzed for the potential to convert intracellular RNA binding proteins TAR DNA binding protein (TDP-43) and Fused in Sarcoma (FUS) into their pathologic prion conformations. The results indicate that the vaccine RNA has specific sequences that may induce TDP-43 and FUS to fold into their pathologic prion confirmations. In the current analysis a total of sixteen UG tandem repeats were identified and additional UG rich sequences were identified. Two GGA sequences were found. Potential G Quadruplex sequences are possibly present but a more sophisticated computer program is needed to verify these. Furthermore, the spike protein, created by the translation of the vaccine RNA, binds angiotensin converting enzyme 2 (ACE2), a zinc containing enzyme. This interaction has the potential to increase intracellular zinc. Zinc ions have been shown to cause the transformation of TDP-43 to its pathologic prion configuration. The folding of TDP-43 and FUS into their pathologic prion confirmations is known to cause ALS, front temporal lobar degeneration, Alzheimer’s disease and other neurological degenerative diseases. The enclosed finding as well as additional potential risks leads the author to believe that regulatory approval of the RNA based vaccines for SARS-CoV-2 was premature and that the vaccine may cause much more harm than benefit.
1) The mRNA vaccines can cause prion disease
2) The folding of TDP-43 and FUS into their pathologic prion confirmations is known to cause ALS, front temporal lobar degeneration, Alzheimer’s disease and other neurological degenerative diseases.
3) The spike protein can increase zinc levels resulting in prion disease
4) The spike protein could be a receptor for a more infectious agent
5) The RNA based COVID vaccines have the potential to cause more disease than the epidemic of COVID-19
6) Prions can be used as a bio-weapon
7) Pfizer’s RNA based COVID-19 vaccine contains many of these RNA sequences that have been shown to have high affinity for TDP-43 or FUS and have the potential to induce chronic degenerative neurological diseases.
8) The interaction is quite concerning given the belief that the virus causing COVID-19, SARS-CoV-2, is a bioweapon and it is possible that the viral spike protein may have been designed to cause prion disease.
9) With mass scale vaccinations, genetic diversity is reduced and as a result, everyone in the population now becomes potentially susceptible to binding with the same infectious agent.
10) Autoimmunity and the opposing condition, metabolic syndrome, infections are associated with the induction of autoantibodies and autoimmune disease making it more than plausible a vaccine could do the same.
11) Research showing that certain RNA binding proteins like TDP-43, FUS and others can be activated to form disease causing prions could be used for bioweapons development. This research is funded by private organizations including the Bill and Melinda Gates Foundation, and Ellison Medical Foundation without national/international oversight.
12) Authors found prion related sequences in the COVID-19 spike protein which were not found in related coronaviruses.
13) Others have reported a case of prion disease, Creutzfeldt-Jakob disease, initially occurring in a man with COVID-19.
14) Warning that the current epidemic of COVID-19 is actually the result of an bioweapons attack released in part by individuals in the United States government.
15) Approving a vaccine, utilizing novel RNA technology without extensive testing is extremely dangerous.
16) The vaccine could be a bioweapon and even more dangerous than the original infection.
