Mike Adams Situation Update 11/02/2021
Nov 2, 2021 21:58:20 GMT -5
Post by OmegaMan on Nov 2, 2021 21:58:20 GMT -5
SCIENCE HORROR: Vaccine spike protein enters cell nuclei, suppresses DNA repair engine of the human body, will unleash explosion of cancer, immunodeficiency, autoimmune disorders and accelerated aging
Tuesday, November 02, 2021 by: Mike Adams
Tags: aging, Autoimmune disorders, badcancer, badhealth, badmedicine, biological weapons, cancer, cell division, chromosomes, DNA damage, DNA repair, gene sequence, genetic code, goodscience, longevity, mutants, mutations, NHEJ, replication, spike protein, telomeres, vaccine damage, vaccines, virology, Zombies
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www.afinalwarning.com/567688.html
(Natural News) This finding can only be described as a true “horror” in its implications. Stunning new research published in Viruses, part of the SARS-CoV-2 Host Cell Interactions edition of MDPI (Open Access Journals) reveals that vaccine spike proteins enter cell nuclei and wreak havoc on cells’ DNA repair mechanism, suppressing DNA repair by as much as 90%.
The research paper is entitled, “SARS–CoV–2 Spike Impairs DNA Damage Repair and Inhibits V(D)J Recombination In Vitro” and is authored by Hui Jiang and Ya-Fang Mei, at the Department of Molecular Biosciences, The Wenner–Gren Institute, Stockholm University, SE-10691 Stockholm, Sweden, and the Department of Clinical Microbiology, Virology, Umeå University, SE-90185 Umeå, Sweden, respectively.
We have saved a copy of the research paper in a PDF document on NN servers at this URL:
www.naturalnews.com/files/viruses-13-02056-v2.pdf
In the conclusion of the paper, authors write, “We found that the spike protein markedly inhibited both BRCA1 and 53BP1 foci formation (Figure 3D–G). Together, these data show that the SARS–CoV–2 full–length spike protein inhibits DNA damage repair by hindering DNA repair protein recruitment.”
The DNA repair mechanism, known as NHEJ (Non-Homologous End Joining) is a kind of intracellular “emergency response” system that repairs double-stranded DNA breaks. Without the NHEJ mechanism, all advanced multi-cellular life would cease to exist. No human being, animal or plant can survive with the integrity of its genetic code being protected and constantly repaired through multiple mechanisms.
DNA damage can be caused by exposure to radiation, chemicals found in foods and personal care products, or even exposure to mammography equipment. Excessive sunlight exposure can also cause DNA breaks, and minor DNA mutations occur spontaneously in all living organisms. Airline pilots, for example, are routinely exposed to ionizing radiation due to flying at altitude.
In a normal, healthy person, the NHEJ mechanism repairs the DNA and prevents a pathogenic mutation from occurring. But in the presence of the vaccine spike protein, NHEJ effectiveness is suppressed by as much as 90%, meaning it is unable to do its job due to the suppressed ability to recruit proteins for repair.
As a result, the following “errors” are introduced into chromosomes inside the nuclei of human cells, all due to the presence of the spike protein from mRNA vaccines:
Mutations or “errors” in the genetic sequence.
DELETIONS of entire segments of genetic code.
INSERTIONS of incorrect segments.
Mixing and matching / permutations of genetic code.
These errors, when expressed through cell division and replication, result in:
An explosion of cancer and cancer tumors throughout the body
Loss of production of immune system B and T cells (i.e. induced immunodeficiency)
Autoimmune disorders
Accelerated aging and reduced telomere length
Loss of functioning of complex organ systems such as circulatory, neurological, endocrine, muskuloskeletal, etc.
Cellular damage resembling radiation poisoning as cells destroy themselves from within
Many of these effects are, of course, fatal. Others will burden vaccine victims with horrendous debilitating injuries and organ malfunctions that will require a lifetime of medical intervention.
Spike protein goes into the nucleus of the cell
From the paper linked above:
Mechanistically, we found that the spike protein localizes in the nucleus and inhibits DNA damage repair by impeding key DNA repair protein BRCA1 and 53BP1 recruitment to the damage site.
This means that the spike protein, which is generated in cell ribosomes after the cells have been hijacked by mRNA vaccines, doesn’t always leave the cell and enter the bloodstream as we are told by mRNA vaccine proponents. In some cases, the spike protein enters the cell nucleus. There, it interferes with the DNA repair mechanism as described throughout this article.
“Surprisingly, we found the abundance of the spike protein in the nucleus (Figure 1A),” concluded study authors.
This means, without question, mRNA vaccines result in chromosomal alterations in the body’s cells. It is confirmation that such vaccines are, indeed, wreaking havoc with genetic integrity and are exhibiting side effects that have not been anticipated or described by mRNA vaccine proponents.
Dr. Thomas Levy writes about the toxicity of the spike protein on Orthomolecular.org:
Concern has been raised regarding the dissemination of the spike protein throughout the body after vaccination. Rather than staying localized at the injection site in order to provoke the immune response and nothing more, spike protein presence has been detected throughout the body of some vaccinated individuals. Furthermore, it appears that some of the circulating spike proteins simply bind the ACE2 receptors without entering the cell, inducing an autoimmune response to the entire cell-spike protein entity. Depending on the cell type that binds the spike protein, any of a number of autoimmune medical conditions can result.
More alarmingly, Dr. Levy explains that current evidence shows the spike protein continues to produced in the body, following the initial mRNA injection. He explains:
While the underlying pathology remains to be completely defined, one explanation for the problems with thrombotic tendencies and other symptomatology seen with chronic COVID and post-vaccination patients relates directly to the persistent presence of the spike protein part of the coronavirus. Some reports assert that the spike protein can continue to be produced after the initial binding to the ACE2 receptors and entry into some of the cells that it initially targets. The clinical pictures of chronic COVID and post-vaccine toxicity appear very similar, and both are likely due to this continued presence, and body-wide dissemination, of the spike protein (Mendelson et al., 2020; Aucott and Rebman, 2021; Levy, 2021; Raveendran, 2021).
Full-length spike protein resulted in the greatest suppression of NHEJ DNA repair mechanism
See the figures below. SARS-CoV-2 viral fragments are named “Nsp1, Nsp5” and so on. The full-length spike is called “Spike” and the nucleocapsid — another structural part of the whole spike protein pathogen — is identified separately.
Article (with charts) continues at link
www.brighteon.com/cb351cd3-6c94-4f2b-a05d-bbda757d4472
Tuesday, November 02, 2021 by: Mike Adams
Tags: aging, Autoimmune disorders, badcancer, badhealth, badmedicine, biological weapons, cancer, cell division, chromosomes, DNA damage, DNA repair, gene sequence, genetic code, goodscience, longevity, mutants, mutations, NHEJ, replication, spike protein, telomeres, vaccine damage, vaccines, virology, Zombies
Bypass censorship by sharing this link:
New
www.afinalwarning.com/567688.html
(Natural News) This finding can only be described as a true “horror” in its implications. Stunning new research published in Viruses, part of the SARS-CoV-2 Host Cell Interactions edition of MDPI (Open Access Journals) reveals that vaccine spike proteins enter cell nuclei and wreak havoc on cells’ DNA repair mechanism, suppressing DNA repair by as much as 90%.
The research paper is entitled, “SARS–CoV–2 Spike Impairs DNA Damage Repair and Inhibits V(D)J Recombination In Vitro” and is authored by Hui Jiang and Ya-Fang Mei, at the Department of Molecular Biosciences, The Wenner–Gren Institute, Stockholm University, SE-10691 Stockholm, Sweden, and the Department of Clinical Microbiology, Virology, Umeå University, SE-90185 Umeå, Sweden, respectively.
We have saved a copy of the research paper in a PDF document on NN servers at this URL:
www.naturalnews.com/files/viruses-13-02056-v2.pdf
In the conclusion of the paper, authors write, “We found that the spike protein markedly inhibited both BRCA1 and 53BP1 foci formation (Figure 3D–G). Together, these data show that the SARS–CoV–2 full–length spike protein inhibits DNA damage repair by hindering DNA repair protein recruitment.”
The DNA repair mechanism, known as NHEJ (Non-Homologous End Joining) is a kind of intracellular “emergency response” system that repairs double-stranded DNA breaks. Without the NHEJ mechanism, all advanced multi-cellular life would cease to exist. No human being, animal or plant can survive with the integrity of its genetic code being protected and constantly repaired through multiple mechanisms.
DNA damage can be caused by exposure to radiation, chemicals found in foods and personal care products, or even exposure to mammography equipment. Excessive sunlight exposure can also cause DNA breaks, and minor DNA mutations occur spontaneously in all living organisms. Airline pilots, for example, are routinely exposed to ionizing radiation due to flying at altitude.
In a normal, healthy person, the NHEJ mechanism repairs the DNA and prevents a pathogenic mutation from occurring. But in the presence of the vaccine spike protein, NHEJ effectiveness is suppressed by as much as 90%, meaning it is unable to do its job due to the suppressed ability to recruit proteins for repair.
As a result, the following “errors” are introduced into chromosomes inside the nuclei of human cells, all due to the presence of the spike protein from mRNA vaccines:
Mutations or “errors” in the genetic sequence.
DELETIONS of entire segments of genetic code.
INSERTIONS of incorrect segments.
Mixing and matching / permutations of genetic code.
These errors, when expressed through cell division and replication, result in:
An explosion of cancer and cancer tumors throughout the body
Loss of production of immune system B and T cells (i.e. induced immunodeficiency)
Autoimmune disorders
Accelerated aging and reduced telomere length
Loss of functioning of complex organ systems such as circulatory, neurological, endocrine, muskuloskeletal, etc.
Cellular damage resembling radiation poisoning as cells destroy themselves from within
Many of these effects are, of course, fatal. Others will burden vaccine victims with horrendous debilitating injuries and organ malfunctions that will require a lifetime of medical intervention.
Spike protein goes into the nucleus of the cell
From the paper linked above:
Mechanistically, we found that the spike protein localizes in the nucleus and inhibits DNA damage repair by impeding key DNA repair protein BRCA1 and 53BP1 recruitment to the damage site.
This means that the spike protein, which is generated in cell ribosomes after the cells have been hijacked by mRNA vaccines, doesn’t always leave the cell and enter the bloodstream as we are told by mRNA vaccine proponents. In some cases, the spike protein enters the cell nucleus. There, it interferes with the DNA repair mechanism as described throughout this article.
“Surprisingly, we found the abundance of the spike protein in the nucleus (Figure 1A),” concluded study authors.
This means, without question, mRNA vaccines result in chromosomal alterations in the body’s cells. It is confirmation that such vaccines are, indeed, wreaking havoc with genetic integrity and are exhibiting side effects that have not been anticipated or described by mRNA vaccine proponents.
Dr. Thomas Levy writes about the toxicity of the spike protein on Orthomolecular.org:
Concern has been raised regarding the dissemination of the spike protein throughout the body after vaccination. Rather than staying localized at the injection site in order to provoke the immune response and nothing more, spike protein presence has been detected throughout the body of some vaccinated individuals. Furthermore, it appears that some of the circulating spike proteins simply bind the ACE2 receptors without entering the cell, inducing an autoimmune response to the entire cell-spike protein entity. Depending on the cell type that binds the spike protein, any of a number of autoimmune medical conditions can result.
More alarmingly, Dr. Levy explains that current evidence shows the spike protein continues to produced in the body, following the initial mRNA injection. He explains:
While the underlying pathology remains to be completely defined, one explanation for the problems with thrombotic tendencies and other symptomatology seen with chronic COVID and post-vaccination patients relates directly to the persistent presence of the spike protein part of the coronavirus. Some reports assert that the spike protein can continue to be produced after the initial binding to the ACE2 receptors and entry into some of the cells that it initially targets. The clinical pictures of chronic COVID and post-vaccine toxicity appear very similar, and both are likely due to this continued presence, and body-wide dissemination, of the spike protein (Mendelson et al., 2020; Aucott and Rebman, 2021; Levy, 2021; Raveendran, 2021).
Full-length spike protein resulted in the greatest suppression of NHEJ DNA repair mechanism
See the figures below. SARS-CoV-2 viral fragments are named “Nsp1, Nsp5” and so on. The full-length spike is called “Spike” and the nucleocapsid — another structural part of the whole spike protein pathogen — is identified separately.
Article (with charts) continues at link
www.brighteon.com/cb351cd3-6c94-4f2b-a05d-bbda757d4472