Los Angeles is now a two-tiered society, and you aren’t allowed to participate unless you’re jabbed with the deadly spike protein

Source: https://www.naturalnews.com/2021-11-11-los-angeles-now-a-two-tiered-society.html

(Natural News) A medical Apartheid is taking root in the United States of America. Los Angeles Democrats have now turned the city into a discriminatory, two-tiered society that celebrates segregation and the loss of medical privacy and ethics.

No one is allowed to participate in this safe, Democrat utopia unless they are jabbed with the deadly, debilitating mRNA vaccines. No one is allowed to visit theaters, restaurants, shopping malls, gyms, salons, etc. if they do not show proof that they were inoculated by this global experiment.

One jab isn’t enough either. Most vaccine programs require a minimum of two shots. Israel now requires three shots and is moving quickly to require a fourth, revoking freedoms for the vaccine compliant every six months.

People who are injured by the first shot cannot medically tolerate a second or a third shot and are therefore barred from society, too. People who are killed or disabled by the second or third shot ultimately lose everything as they try to comply with evil.

Pain, misery, death, segregation and total subservience: the Democrat’s safe utopia

This experimental gene interference technology encodes lab engineered spike proteins inside the body. In addition to all the other adverse events commonly caused by vaccines (including Guillain Barre syndrome, anaphylaxis and Bell’s Palsy), these foreign toxins cause blood clots and permanent damage to the recipient’s cardiovascular system, including damage to their myocardium and pericardium.

Data is beginning to show that the shots also increase one’s susceptibility to infection, wiping out critical facets of the innate immune system. This leads to lifelong dependence on mRNA updates, or however many shots it takes to kill a person.

Study – SARS-CoV-2 Spike Protein Elicits Cell Signaling in Human Host Cells: Implications for Possible Consequences of COVID-19 Vaccines

Stars: https://pubmed.ncbi.nlm.nih.gov/33440640/

Abstract

The world is suffering from the coronavirus disease 2019 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). SARS-CoV-2 uses its spike protein to enter the host cells. Vaccines that introduce the spike protein into our body to elicit virus-neutralizing antibodies are currently being developed. In this article, we note that human host cells sensitively respond to the spike protein to elicit cell signaling. Thus, it is important to be aware that the spike protein produced by the new COVID-19 vaccines may also affect the host cells. We should monitor the long-term consequences of these vaccines carefully, especially when they are administered to otherwise healthy individuals. Further investigations on the effects of the SARS-CoV-2 spike protein on human cells and appropriate experimental animal models are warranted.

Study – The furin cleavage site in the SARS-CoV-2 spike protein is required for transmission in ferrets

Source: https://pubmed.ncbi.nlm.nih.gov/33907312/

Abstract

SARS-CoV-2 entry requires sequential cleavage of the spike glycoprotein at the S1/S2 and the S2′ cleavage sites to mediate membrane fusion. SARS-CoV-2 has a polybasic insertion (PRRAR) at the S1/S2 cleavage site that can be cleaved by furin. Using lentiviral pseudotypes and a cell-culture-adapted SARS-CoV-2 virus with an S1/S2 deletion, we show that the polybasic insertion endows SARS-CoV-2 with a selective advantage in lung cells and primary human airway epithelial cells, but impairs replication in Vero E6, a cell line used for passaging SARS-CoV-2. Using engineered spike variants and live virus competition assays and by measuring growth kinetics, we find that the selective advantage in lung and primary human airway epithelial cells depends on the expression of the cell surface protease TMPRSS2, which enables endosome-independent virus entry by a route that avoids antiviral IFITM proteins. SARS-CoV-2 virus lacking the S1/S2 furin cleavage site was shed to lower titres from infected ferrets and was not transmitted to cohoused sentinel animals, unlike wild-type virus. Analysis of 100,000 SARS-CoV-2 sequences derived from patients and 24 human postmortem tissues showed low frequencies of naturally occurring mutants that harbour deletions at the polybasic site. Taken together, our findings reveal that the furin cleavage site is an important determinant of SARS-CoV-2 transmission.

banned.video – Dr. Peter McCullough Issues Emergency Warning: Vaccine Created Spike Protein is Deadly in the Human Body

See the video here: https://banned.video/watch?id=6185b407e19ed5372ded8319

Dr. Peter McCullough joins The Alex Jones Show to issue a warning to the public and expose corruption behind the growing medical tyranny state.

SARS–CoV–2 Spike Impairs DNA Damage Repair and Inhibits V(D)J Recombination In Vitro

Source: https://www.mdpi.com/1999-4915/13/10/2056/htm

PDF: https://www.naturalnews.com/files/viruses-13-02056-v2.pdf

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS–CoV–2) has led to the coronavirus disease 2019 (COVID–19) pandemic, severely affecting public health and the global economy. Adaptive immunity plays a crucial role in fighting against SARS–CoV–2 infection and directly influences the clinical outcomes of patients. Clinical studies have indicated that patients with severe COVID–19 exhibit delayed and weak adaptive immune responses; however, the mechanism by which SARS–CoV–2 impedes adaptive immunity remains unclear. 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.

More on the subject here: 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#

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

(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.

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.