[D66] [JD: 121] Worse Than the Disease? Reviewing Some Possible Unintended Consequences of the mRNA Vaccines Against COVID-19

[R.O.]

https://ijvtpr.com/index.php/IJVTPR/article/view/23

 Worse Than the Disease? Reviewing Some Possible Unintended Consequences
of the mRNA Vaccines Against COVID-19
Authors

    Stephanie Seneff Computer Science and Artificial Intelligence
Laboratory, MIT, Cambridge MA, 02139, USA
    Greg Nigh Naturopathic Oncology, Immersion Health, Portland, OR
97214, USA

Keywords: antibody dependent enhancement, autoimmune diseases, gene
editing, lipid nanoparticles, messenger RNA, prion diseases, reverse
transcription, SARS-CoV-2 vaccines

Abstract

Operation Warp Speed brought to market in the United States two mRNA
vaccines, produced by Pfizer and Moderna. Interim data suggested high
efficacy for both of these vaccines, which helped legitimize Emergency
Use Authorization (EUA) by the FDA. However, the exceptionally rapid
movement of these vaccines through controlled trials and into mass
deployment raises multiple safety concerns. In this review we first
describe the technology underlying these vaccines in detail. We then
review both components of and the intended biological response to these
vaccines, including production of the spike protein itself, and their
potential relationship to a wide range of both acute and long-term
induced pathologies, such as blood disorders, neurodegenerative diseases
and autoimmune diseases. Among these potential induced pathologies, we
discuss the relevance of prion-protein-related amino acid sequences
within the spike protein. We also present a brief review of studies
supporting the potential for spike protein “shedding”, transmission of
the protein from a vaccinated to an unvaccinated person, resulting in
symptoms induced in the latter. We finish by addressing a common point
of debate, namely, whether or not these vaccines could modify the DNA of
those receiving the vaccination. While there are no studies
demonstrating definitively that this is happening, we provide a
plausible scenario, supported by previously established pathways for
transformation and transport of genetic material, whereby injected mRNA
could ultimately be incorporated into germ cell DNA for
transgenerational transmission. We conclude with our recommendations
regarding surveillance that will help to clarify the long-term effects
of these experimental drugs and allow us to better assess the true
risk/benefit ratio of these novel technologies.

Author Biographies

Stephanie Seneff, Computer Science and Artificial Intelligence
Laboratory, MIT, Cambridge MA, 02139, USA
Computer Science and Artificial Intelligence Laboratory, MIT, Cambridge
MA, 02139, USA

Greg Nigh, Naturopathic Oncology, Immersion Health, Portland, OR 97214, USA
Naturopathic Oncology, Immersion Health, Portland, OR 97214, USA