Innate immune suppression by SARS-CoV-2 mRNA vaccinations: The role of G-quadruplexes, exosomes, and MicroRNAs

The mRNA SARS-CoV-2 vaccines were brought to market in response to the public health crises of Covid-19. The utilization of mRNA vaccines in the context of infectious disease has no precedent. The many alterations in the vaccine mRNA hide the mRNA from cellular defenses and promote a longer biologic...

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Published inFood and chemical toxicology Vol. 164; p. 113008
Main Authors Seneff, Stephanie, Nigh, Greg, Kyriakopoulos, Anthony M., McCullough, Peter A.
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.06.2022
The Authors. Published by Elsevier Ltd
Subjects
adaptive immunity
biological half-life
Cancer
carcinogenesis
COVID-19 - prevention & control
COVID-19 infection
COVID-19 Vaccines - adverse effects
DNA damage
Exosomes
Exosomes - metabolism
G-Quadruplexes
human health
Humans
immune response
Immunity, Innate
interferons
liver diseases
markets
microRNA
microRNAs
MicroRNAs - genetics
MicroRNAs - metabolism
monitoring
mRNA Vaccines - adverse effects
myocarditis
neurodegenerative diseases
Neurodegenerative Diseases - metabolism
protein synthesis
public health
risk
RNA, Messenger - genetics
RNA, Messenger - metabolism
SARS-CoV-2
SARS-CoV-2 mRNA vaccines
Severe acute respiratory syndrome coronavirus 2
Spike Glycoprotein, Coronavirus
thrombocytopenia
toxicology
Type I interferon Response
vaccination
Vaccination - adverse effects
vaccines
Vaccines, Synthetic - adverse effects
microRNAs
G-quadruplexes
Type I interferon Response
Exosomes
SARS-CoV-2 mRNA vaccines
Cancer
Online AccessGet full text
ISSN0278-6915
1873-6351
1873-6351
DOI10.1016/j.fct.2022.113008

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Abstract The mRNA SARS-CoV-2 vaccines were brought to market in response to the public health crises of Covid-19. The utilization of mRNA vaccines in the context of infectious disease has no precedent. The many alterations in the vaccine mRNA hide the mRNA from cellular defenses and promote a longer biological half-life and high production of spike protein. However, the immune response to the vaccine is very different from that to a SARS-CoV-2 infection. In this paper, we present evidence that vaccination induces a profound impairment in type I interferon signaling, which has diverse adverse consequences to human health. Immune cells that have taken up the vaccine nanoparticles release into circulation large numbers of exosomes containing spike protein along with critical microRNAs that induce a signaling response in recipient cells at distant sites. We also identify potential profound disturbances in regulatory control of protein synthesis and cancer surveillance. These disturbances potentially have a causal link to neurodegenerative disease, myocarditis, immune thrombocytopenia, Bell's palsy, liver disease, impaired adaptive immunity, impaired DNA damage response and tumorigenesis. We show evidence from the VAERS database supporting our hypothesis. We believe a comprehensive risk/benefit assessment of the mRNA vaccines questions them as positive contributors to public health. [Display omitted] •mRNA vaccines promote sustained synthesis of the SARS-CoV-2 spike protein.•The spike protein is neurotoxic, and it impairs DNA repair mechanisms.•Suppression of type I interferon responses results in impaired innate immunity.•The mRNA vaccines potentially cause increased risk to infectious diseases and cancer.•Codon optimization results in G-rich mRNA that has unpredictable complex effects.
AbstractList The mRNA SARS-CoV-2 vaccines were brought to market in response to the public health crises of Covid-19. The utilization of mRNA vaccines in the context of infectious disease has no precedent. The many alterations in the vaccine mRNA hide the mRNA from cellular defenses and promote a longer biological half-life and high production of spike protein. However, the immune response to the vaccine is very different from that to a SARS-CoV-2 infection. In this paper, we present evidence that vaccination induces a profound impairment in type I interferon signaling, which has diverse adverse consequences to human health. Immune cells that have taken up the vaccine nanoparticles release into circulation large numbers of exosomes containing spike protein along with critical microRNAs that induce a signaling response in recipient cells at distant sites. We also identify potential profound disturbances in regulatory control of protein synthesis and cancer surveillance. These disturbances potentially have a causal link to neurodegenerative disease, myocarditis, immune thrombocytopenia, Bell's palsy, liver disease, impaired adaptive immunity, impaired DNA damage response and tumorigenesis. We show evidence from the VAERS database supporting our hypothesis. We believe a comprehensive risk/benefit assessment of the mRNA vaccines questions them as positive contributors to public health.The mRNA SARS-CoV-2 vaccines were brought to market in response to the public health crises of Covid-19. The utilization of mRNA vaccines in the context of infectious disease has no precedent. The many alterations in the vaccine mRNA hide the mRNA from cellular defenses and promote a longer biological half-life and high production of spike protein. However, the immune response to the vaccine is very different from that to a SARS-CoV-2 infection. In this paper, we present evidence that vaccination induces a profound impairment in type I interferon signaling, which has diverse adverse consequences to human health. Immune cells that have taken up the vaccine nanoparticles release into circulation large numbers of exosomes containing spike protein along with critical microRNAs that induce a signaling response in recipient cells at distant sites. We also identify potential profound disturbances in regulatory control of protein synthesis and cancer surveillance. These disturbances potentially have a causal link to neurodegenerative disease, myocarditis, immune thrombocytopenia, Bell's palsy, liver disease, impaired adaptive immunity, impaired DNA damage response and tumorigenesis. We show evidence from the VAERS database supporting our hypothesis. We believe a comprehensive risk/benefit assessment of the mRNA vaccines questions them as positive contributors to public health.
The mRNA SARS-CoV-2 vaccines were brought to market in response to the public health crises of Covid-19. The utilization of mRNA vaccines in the context of infectious disease has no precedent. The many alterations in the vaccine mRNA hide the mRNA from cellular defenses and promote a longer biological half-life and high production of spike protein. However, the immune response to the vaccine is very different from that to a SARS-CoV-2 infection. In this paper, we present evidence that vaccination induces a profound impairment in type I interferon signaling, which has diverse adverse consequences to human health. Immune cells that have taken up the vaccine nanoparticles release into circulation large numbers of exosomes containing spike protein along with critical microRNAs that induce a signaling response in recipient cells at distant sites. We also identify potential profound disturbances in regulatory control of protein synthesis and cancer surveillance. These disturbances potentially have a causal link to neurodegenerative disease, myocarditis, immune thrombocytopenia, Bell's palsy, liver disease, impaired adaptive immunity, impaired DNA damage response and tumorigenesis. We show evidence from the VAERS database supporting our hypothesis. We believe a comprehensive risk/benefit assessment of the mRNA vaccines questions them as positive contributors to public health. Image 1
The mRNA SARS-CoV-2 vaccines were brought to market in response to the public health crises of Covid-19. The utilization of mRNA vaccines in the context of infectious disease has no precedent. The many alterations in the vaccine mRNA hide the mRNA from cellular defenses and promote a longer biological half-life and high production of spike protein. However, the immune response to the vaccine is very different from that to a SARS-CoV-2 infection. In this paper, we present evidence that vaccination induces a profound impairment in type I interferon signaling, which has diverse adverse consequences to human health. Immune cells that have taken up the vaccine nanoparticles release into circulation large numbers of exosomes containing spike protein along with critical microRNAs that induce a signaling response in recipient cells at distant sites. We also identify potential profound disturbances in regulatory control of protein synthesis and cancer surveillance. These disturbances potentially have a causal link to neurodegenerative disease, myocarditis, immune thrombocytopenia, Bell's palsy, liver disease, impaired adaptive immunity, impaired DNA damage response and tumorigenesis. We show evidence from the VAERS database supporting our hypothesis. We believe a comprehensive risk/benefit assessment of the mRNA vaccines questions them as positive contributors to public health.
The mRNA SARS-CoV-2 vaccines were brought to market in response to the public health crises of Covid-19. The utilization of mRNA vaccines in the context of infectious disease has no precedent. The many alterations in the vaccine mRNA hide the mRNA from cellular defenses and promote a longer biological half-life and high production of spike protein. However, the immune response to the vaccine is very different from that to a SARS-CoV-2 infection. In this paper, we present evidence that vaccination induces a profound impairment in type I interferon signaling, which has diverse adverse consequences to human health. Immune cells that have taken up the vaccine nanoparticles release into circulation large numbers of exosomes containing spike protein along with critical microRNAs that induce a signaling response in recipient cells at distant sites. We also identify potential profound disturbances in regulatory control of protein synthesis and cancer surveillance. These disturbances potentially have a causal link to neurodegenerative disease, myocarditis, immune thrombocytopenia, Bell's palsy, liver disease, impaired adaptive immunity, impaired DNA damage response and tumorigenesis. We show evidence from the VAERS database supporting our hypothesis. We believe a comprehensive risk/benefit assessment of the mRNA vaccines questions them as positive contributors to public health. [Display omitted] •mRNA vaccines promote sustained synthesis of the SARS-CoV-2 spike protein.•The spike protein is neurotoxic, and it impairs DNA repair mechanisms.•Suppression of type I interferon responses results in impaired innate immunity.•The mRNA vaccines potentially cause increased risk to infectious diseases and cancer.•Codon optimization results in G-rich mRNA that has unpredictable complex effects.
ArticleNumber 113008
Author Nigh, Greg
Kyriakopoulos, Anthony M.
Seneff, Stephanie
McCullough, Peter A.
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  orcidid: 0000-0001-8191-1049
  surname: Seneff
  fullname: Seneff, Stephanie
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  organization: Computer Science and Artificial Intelligence Laboratory, MIT, Cambridge, MA, USA, 02139
– sequence: 2
  givenname: Greg
  surname: Nigh
  fullname: Nigh, Greg
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– sequence: 3
  givenname: Anthony M.
  surname: Kyriakopoulos
  fullname: Kyriakopoulos, Anthony M.
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  organization: Research and Development, Nasco AD Biotechnology Laboratory, Department of Research and Development, Sachtouri 11, 18536, Piraeus, Greece
– sequence: 4
  givenname: Peter A.
  surname: McCullough
  fullname: McCullough, Peter A.
  email: peteramccullough@gmail.com
  organization: Truth for Health Foundation, Tucson, AZ, USA
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ISSN 0278-6915
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IngestDate Thu Aug 21 14:11:38 EDT 2025
Fri Sep 05 08:31:20 EDT 2025
Fri Sep 05 03:45:12 EDT 2025
Mon Jul 21 06:04:41 EDT 2025
Tue Jul 01 00:20:40 EDT 2025
Thu Apr 24 23:10:50 EDT 2025
Fri Feb 23 02:40:14 EST 2024
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Keywords microRNAs
G-quadruplexes
Type I interferon Response
Exosomes
SARS-CoV-2 mRNA vaccines
Cancer
Language English
License This is an open access article under the CC BY license.
Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.
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Snippet The mRNA SARS-CoV-2 vaccines were brought to market in response to the public health crises of Covid-19. The utilization of mRNA vaccines in the context of...
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SubjectTerms adaptive immunity
biological half-life
Cancer
carcinogenesis
COVID-19 - prevention & control
COVID-19 infection
COVID-19 Vaccines - adverse effects
DNA damage
Exosomes
Exosomes - metabolism
G-Quadruplexes
human health
Humans
immune response
Immunity, Innate
interferons
liver diseases
markets
microRNA
microRNAs
MicroRNAs - genetics
MicroRNAs - metabolism
monitoring
mRNA Vaccines - adverse effects
myocarditis
neurodegenerative diseases
Neurodegenerative Diseases - metabolism
protein synthesis
public health
risk
RNA, Messenger - genetics
RNA, Messenger - metabolism
SARS-CoV-2
SARS-CoV-2 mRNA vaccines
Severe acute respiratory syndrome coronavirus 2
Spike Glycoprotein, Coronavirus
thrombocytopenia
toxicology
Type I interferon Response
vaccination
Vaccination - adverse effects
vaccines
Vaccines, Synthetic - adverse effects
Title Innate immune suppression by SARS-CoV-2 mRNA vaccinations: The role of G-quadruplexes, exosomes, and MicroRNAs
URI https://dx.doi.org/10.1016/j.fct.2022.113008
https://www.ncbi.nlm.nih.gov/pubmed/35436552
https://www.proquest.com/docview/2652583793
https://www.proquest.com/docview/2661026075
https://pubmed.ncbi.nlm.nih.gov/PMC9012513
Volume 164
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