HORRIFIC STUDY: COVID-19 Jab Spike Protein Enters Cell Nuclei, Suppresses DNA Repair, And Causes Cancer & Autoimmune Disorders

A new study published in Viruses describes catastrophic cellular damage caused by the spike protein from the experimental COVID-19 injections.

The research indicates that once spike proteins enter the cell nuclei, it suppresses a DNA repair mechanism inside the body.

This DNA repair mechanism, known as NHEJ (Non-Homologous End Joining), is suppressed by as much as 90%.

Deterioration of this cellular function can lead to:

-Cancerous tumors

-Induced immunodeficiency

-Autoimmune disorders

-Misfunction of organ systems

-Cellular damage

https://www.naturalnews. com/2021-11-02-science-horror-vaccine-spike-protein-enters-cell-nuclei-suppresses-dna-repair-engine-of-the-human-body-cancer-aging.html pic.twitter.com/c1hTy5tlPv

— :Déjà vu-Terriers (@TerriersVu) November 2, 2021

https://twitter.com/tarafdavis/status/1455900380529893376

https://t.co/poyGkNVMwi
SCIENCE HORROR: Vaccine Spike Protein Enters Cell Nuclei, Suppresses DNA Repair Engine – Will Unleash Explosion of Cancer, Immunodeficiency, Autoimmune Disorders and Accelerated Aging pic.twitter.com/he6fG6KBhC

— WITSNEWS (@witsnewsdotcom) November 3, 2021

Titled “SARS–CoV–2 Spike Impairs DNA Damage Repair and Inhibits V(D)J Recombination In Vitro,” the research describes the following:

Here, by using an in vitro cell line, we report that the SARS–CoV–2 spike protein significantly inhibits DNA damage repair, which is required for effective V(D)J recombination in adaptive immunity. 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. Our findings reveal a potential molecular mechanism by which the spike protein might impede adaptive immunity and underscore the potential side effects of full-length spike-based vaccines.

Natural News highlighted the consequences of NHEJ suppression:

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.

Production of the vaccine-induced spike proteins can cause catastrophic injuries and lifelong health consequences for victims.

Natural News highlights the spike protein’s impact on the cell nuclei:

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.

Thomas E. Levy, MD, JD wrote about spike protein toxicity and spike protein production induced by the mRNA injections at Orthomolecular.org:

Spike proteins are the spear-like appendages attached to and completely surrounding the central core of the COVID virus, giving the virion somewhat of a porcupine-like appearance. Upon binding to the angiotensin converting enzyme 2 (ACE2) receptors on the cell membranes of the target cells, dissolving enzymes are released that then permit entry of the complete COVID virus into the cytoplasm, where replication of the virus can ensue (Belouzard et al., 2012; Shang et al., 2020).

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.

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).

Although they are found on many different types of cells throughout the body, the ACE2 receptors on the epithelial cells lining the airways are the first targets of the COVID virus upon initial encounter when inhaled (Hoffman et al., 2020). Furthermore, the concentration of these receptors is especially high on lung alveolar epithelial cells, further causing the lung tissue to be disproportionately targeted by the virus (Alifano et al., 2020). Unchecked, this avid receptor binding and subsequent viral replication inside the lung cells leads directly to low blood oxygen levels and the adult respiratory distress syndrome [ARDS] (Batah and Fabro, 2021). Eventually there is a surge of intracellular oxidation known as the cytokine storm, and death from respiratory failure results (Perrotta et al., 2020; Saponaro et al., 2020; Hu et al., 2021).