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Published Volume 5 | Issue 1 | 1 of 3 Microbiol Infect Dis, 2021

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 (ΨGΨG) were identified and additional UG (ΨG) rich sequences were identified. Two GGΨA 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.

Published Volume 5 | Issue 1 | 1 of 3 Microbiol Infect Dis, 2021 **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.** I*n the current analysis a total of sixteen UG tandem repeats (ΨGΨG) were identified and additional UG (ΨG) rich sequences were identified*. Two GGΨA 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**.

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At this point I doubt it, the vaccine uses the RNA of the spike protein and it gets delivered into your cell and makes your own cells produce the spike protein. If it accidentally mutates into your DNA, you’re kinda fucked.

The spike proteins these people could be or are shedding don’t invade your cells, they can attach to the outside of your cell but without a nucleus it can’t reproduce. If you’re around someone shedding the spike protein from the vaccine for a prolonged period you could possibly feel slightly run down for a few days.

It would just be your immune system destroying the spike proteins that got into your system. Which could possibly also make you immune second hand, which they probably don’t want, it ruins their plans.

Your body has been trained since birth to know spike proteins are bad and goes into overdrive trying to contain it, that’s why you’re already seeing deaths and people experiencing all kinds of side effects of various organs/systems from the vaccine.

Usually the Spike protein attaches to the cell then the nucleus invades the cell and replicates. There’s a research paper out by Harvard scientists showing that the N protein(nucleus) on occasion mutates into your DNA, of course it was “debunked” but other rna viruses can/have do the same thing.

They conclude it could possibly be the cause of “long haul syndrome” that can last from weeks to forever depending on and if your body clears the nucleus encoded DNA cells, it’s more of an annoyance then a direct threat, that a spike protein would cause.

The thing is it happens on rare occasions naturally when you catch a virus. But the government and big pharma are purposely using an experimental delivery system and inserting spike protein RNA into a persons cell while saying it’s perfectly safe. Nobody knows at what rate the mutation occurs naturally in the general population with the Nucleus protein but from reading it would be much higher with the vaccine and the spike protein, how much higher is anyone’s guess at this point.