The study abstract, well worth reading, summarizes both the context, intention, and results of the investigation:
“Development of new vaccine technology has been plagued with problems in the past. The current RNA based SARSCoV-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. [emphasis added]”
As you can see above, the author is clearly concerned about the fact that the novel mRNA-based Covid-19 vaccines presently being deployed to hundreds of millions within the US, and around the world, have both been plagued by problems in the past, and are presently being allowed to bypass proper safety and efficacy testing normally required for FDA approval, through an Emergency Use Authorization enacted on Feb 4th, 2020, which indemnifed manufacturers from liability, and which was made possible through the declaration of national health emergency (now known to be based on faulty disease modeling, Covid death statistics, and faulty PCR-based Covid case numbers) and the emergency medical powers invoked, thereof.
Creutzfeldt–Jakob disease (CJD), also known as neurocognitive disorder or subacute spongiform encephalopathy is due to prion disease, a rapidly progressing and highly fatal degenerative brain disorder
The research, therefore, sought to evaluate and identify the possibility that one of the unintended, adverse effects of the vaccines (specifically, the Pfizer vaccine) may be that either the synthetic nucleoside-mRNA sequence chosen for these vaccines or the spike protein target interaction following their administration may result in the pathological misfolding of proteins normally present in cells, transforming them into what are known as prions -- which can lead to rapid and highly lethal brain degeneration related disorders. [To learn more about prion diseases, you can get a summary at the PrionAlliance.com website]
The research uncovered that, indeed, a plausible mechanism for mRNA Covid-19-induced prion formation exists, namely, “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 study points that previous research has been done that indicates there is a link between COVID-19 vaccines and prion disease:
