Analysis by Dr. Joseph Mercola
Story at-a-glance
- The COVID shots reprogram your immune system to respond in a dysfunctional manner. Aside from increasing vulnerability to infections, this can also result in autoimmune diseases and cancer
- A paper published in early May 2021 reported the Pfizer/BioNTech COVID jab “reprograms both adaptive and innate immune responses,” causing immune depletion
- Antigens in vaccines have been shown to induce defects in the immune system that can raise the risk of autoimmune diseases
- Leaky or nonsterilizing vaccines can also trigger the evolution of more hazardous viruses, and the COVID jabs are among the leakiest “vaccines” ever created
- According to health authorities, the vaccine-evading Omicron variant necessitates a third COVID injection, but this recommendation will only perpetuate mutation
A number of medical experts, scientists and published studies now warn that the COVID shots reprogram your immune system to respond in a dysfunctional manner.
Aside from increasing vulnerability to infections, this can also result in autoimmune diseases and cancer.
Pfizer Shot Reprograms Both Arms of Your Immune System
A paper1 posted May 6, 2021, on the preprint server medRxiv reported that the Pfizer/BioNTech COVID jab
"reprograms both adaptive and innate immune responses," causing immune depletion.
While they confirmed the jab "induced effective humoral and cellular immunity against several SARS-CoV-2 variants," the shot
"also modulated the production of inflammatory cytokines by innate immune cells upon stimulation with both specific (SARS-CoV-2) and nonspecific (viral, fungal and bacterial) stimuli."
In other words, we're looking at a horrible tradeoff. You may get some protection against SARS-CoV-2 and its variants, but you're weakening your overall immune function, which opens the door wide to all sorts of other health problems,
from bacterial, fungal and viral infections to cancer and autoimmunity.
After the injection, innate immune cells had a markedly decreased response to toll-like receptors 4, 7 and 8 (TLR4, TLR7, TLR8) ligands, while cytokine responses induced by fungi were stronger. According to the authors, defects in TLR7 have previously been linked to an increased susceptibility to COVID-19 in young males.
People who were "fully vaccinated," having received two doses of the Pfizer shot, also produced significantly less interferon upon stimulation, and this can hamper the initial innate immune response against the virus.
Repeated Vaccinations and the Risk of Autoimmunity
Pathogenic infections and cancer are but two potential outcomes of this kind of reprogramming. Previous research,
for example, has linked defects in the immune system to a higher risk of autoimmune diseases. What's more, it's been shown that antigens in vaccines, specifically, can induce this kind of immune system dysfunction.2 As reported in the paper in question:3
"Repeated immunization with antigen causes systemic autoimmunity in mice otherwise not prone to spontaneous autoimmune diseases. Overstimulation of CD4+ T cells led to the development of autoantibody-inducing CD4+ T (aiCD4+ T) cell which had undergone T cell receptor (TCR) revision and was capable of inducing autoantibodies.
The aiCD4+ T cell was induced by de novo TCR revision but not by cross-reaction, and subsequently overstimulated CD8+ T cells, driving them to become antigen-specific cytotoxic T lymphocytes (CTL).
These CTLs could be further matured by antigen cross-presentation, after which they caused autoimmune tissue injury akin to systemic lupus erythematosus (SLE). Systemic autoimmunity appears to be the inevitable consequence of over-stimulating the host's immune 'system' by repeated immunization with antigen, to the levels that surpass system's self-organized criticality."
Fast-forward to mid-May 2021, when a study4 in the Journal of Clinical Investigations reported that "SARS-CoV-2 mRNA vaccines induce broad CD4+ T cell responses that recognize SARS-CoV-2 variants and HCoV-NL63." HCoV-NL63 is a human coronavirus associated with the common cold.
"Interestingly, we observed a 3-fold increase in the CD4+ T cell responses to HCoV-NL63 spike peptides after vaccination," the authors stated, adding, "Our results suggest that T cell responses elicited or enhanced by SARS-CoV-2 mRNA vaccines may be able to control SARS-CoV-2 variants and lead to cross-protection against some endemic coronaviruses."
What they did not address was
that excessive CD4a+ T cell responses could also result in the development of autoantibodies and autoimmune disease.
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