The spike protein behaves as a hapten, a small molecule that binds to the surface of organs, leading to an autoimmune response.
The spike protein can damage organs directly by promoting cardiovascular complications, damaging blood vessels in the lungs, and breaking through the blood brain barrier (BBB), important for protecting the brain.
The spike protein can incorporate into human DNA through a process called transfection.
The spike protein evokes the release of destructive anti-spike-antibodies, [anti-S-Ab] discussed below.
MOI #1: Injections can lead to death through anaphylactic shock, a life-threatening allergic reaction. With COVID shots, the allergic reaction is suspected to be caused by previous exposure to and sensitization to polyethylene glycol [PEG].
MOI #2: Anti-Inflammatory macrophages, called M2, are inhibited by anti-spike-antibodies [antiS-Ab]
MOI #3: All COVID shots lead to the creation of a spike protein through a process called translation. The spike protein can damage the body by at least FOUR pathways:
1) The spike protein behaves as a hapten, a small molecule that binds to the surface of organs, leading to an autoimmune response.
2) The spike protein can damage organs directly by promoting cardiovascular complications, damaging blood vessels in the lungs, and breaking through the blood brain barrier (BBB), important for protecting the brain.
3) The spike protein can incorporate into human DNA through a process called transfection.
4) The spike protein evokes the release of destructive anti-spike-antibodies, [anti-S-Ab] discussed below
MOI #4: Spike protein can trigger changes in blood vessel walls, leading to pulmonary artery hypertension (PAH), which is fatal even under the best current conventional and alternative treatments.
MOI #5: The spike protein can bind to the ACE2 receptor on surface of sperm and ovaries. Risk of infertility is high but not yet proven.
MOI #6: Spike proteins cause inflammation and disruption of the blood brain barrier (BBB), leading to neuropathology and brain degeneration.
MOI #7: Neurological degeneration: spike proteins can damage the FUS gene and mutate the TDP-43 protein, leading to Amyotrophic Lateral Sclerosis (ALS).
MOI #8: Neurological degeneration: mutation and altered function of the TDP-43 protein can also lead to frontotemporal lobe degeneration (FTLD), a cluster of chronic, degenerative neurological diseases
MOI #9: Mutation of the FUS gene can also lead to cancer.
MOI #10: Adenoviruses used in both the Johnson & Johnson shot and the AstraZeneca shots pose a risk of cancer.
MOI #11: Anti-spike-antibodies [anti-S-Ab] can cause significant organ damage, specifically to the lungs. The antibodies can also cross-react with 28 different human tissue types, establishing a mechanism for multi-system autoimmune disorders and multi-organ failure.
MOI #12: Previous coronavirus exposure and the concept called ‘original antigenic sin’ stops true protection against the SARS-CoV-2 if a person has been previously ill with a common coronavirus infection.
MOI #13: There is an increased risk of COVID illness and COVID-related death in people who have had a previous influenza vaccine.
MOI #14: The larger (highly elevated) SARS-CoV-2 antibody response from a COVID infection or from a COVID shot, results in prolonged and more severe illness.
MOI #15: COVID shots can lead to enlarged lymph nodes that may have long term ramifications.
MOI #16: Widespread use of COVID shots results in non-neutralizing antibodies, especially in people who have already had a COVID infection. This may be leading to virulent mutant viruses
MOI #17: Antibody Dependent Enhancement (ADE) is a phenomenon occurs when a person is exposed to a circulating coronavirus after being vaccinated. The anti-S-Ab enhances the entry of the SARS-CoV-2 virus into the cell (usually macrophages) and accelerates its replication, causing more severe illness than they would have experienced if they had not been vaccinated.
MOI #18: Johnson/Johnson and AstraZeneca shots release a transgene that can lead to potentially deadly side effects from injecting raw genetic material that can induce anti-DNA antibodies and can integrate into human DNA.
MOI #19: Both Johnson/Johnson and AstraZeneca shots carry a snip of double stranded DNA (dsDNA) [transgene] wrapped in an adenovirus outer “shell.” 50-billion particles are injected with each injection. dsDNA-antibodies are diagnostic of a long list of autoimmune disorders.
MOI #20 – The AstraZeneca shot has been known to be associated with potentially deadly blood clots, a condition named Vaccine-Induced Prothrombotic Immune Thrombocytopenia (VIPIT).
“Approving a vaccine, utilizing novel RNA technology without extensive testing is extremely dangerous. The vaccine could be a bioweapon and even more dangerous than the original infection.”
* REF: Classen JB. COVID-19 RNA Based Vaccines and the Risk of Prion Disease. Microbiol Infect Dis. 2021; 5(1):1-3.
https://scivisionpub.com/pdfs/covid19-rna-based-vaccines-and-the-risk-of-prion-disease-1503.pdf
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By injecting the synthetically made SARS-CoV-2 spike protein into the entire population through these genetic-modification injections, the risk of longterm side effects and risk of developing an autoimmune illness will remain for an unknown period of time.
However, with B-cell priming and irreversible genetic manipulation, the risk for developing chronic illness or sudden death could last forever.
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Résume uit: 20MOI E-book By Dr. Sherri Tenpenny.PDF
te bestellen via https://www.drtenpenny.com/ebook-20-moi
