Why the Body Attacks Itself after COVID-19 Vaccination
Autoimmunity is a Direct Consequence of Poorly Conceived Genetic Vaccines
By Peter A. McCullough, MD, MPH
The human immune system is designed to recognize foreign invaders (microbes, other substances) attack, kill, and then clear the debris away. For that reason, we must be sure that our bodies recognize our own cells as “protected” and the foreign ones as targets. For the first time, mRNA (Pfizer, Moderna) and adenoviral DNA (Janssen) COVID-19 vaccines install the genetic code for our bodies to make a deadly foreign protein with the aspiration that our immune system would not only respond and protect us, but also form live saving immunity from SARS-CoV-2. We have come to learn this was the drug development miscalculation of all time. Production of a foreign protein in the human body has turned out to be a disaster as illustrated by Polykretis et al in a recent paper. Here are some of the reasons why: 1) each cell that takes up the vaccine expresses the protein in the cell surface initiating autoimmune attack, 2) the tissue distribution appears to be wide involving organs where this attack could be lethal (heart, brain, bone marrow, etc.), 3) both the genetic material and the Spike protein are long lasting (months to years) which is long enough to cause an autoimmune syndrome which may be permanent.
Polykretis elaborates: “ Strong histological evidence from biopsies and autopsies have demonstrated that the vaccine-derived spike protein was synthesized in terminally differentiated tissues (Baumeier et al., 2022; Schwab et al., 2022; Mörz, 2022). Baumeier et al. detected the vaccine-derived spike protein on the cardiomyocytes of 9 out of 15 patients with clinical suspicion of myocarditis (which were negatively tested for SARS-CoV-2), proving that the viral protein has been synthesized in the heart tissue and suggesting an autoimmune response due to vaccination (Baumeier et al., 2022). Schwab et al. describe the histopathological findings from standardized autopsies performed on 25 people who had passed away unexpectedly and within 20 days from vaccination (none of the deceased persons had SARS-CoV-2 infection prior to vaccination) (Schwab et al., 2022). Both the aforementioned studies support the idea that vaccine-induced myocardial inflammation was a consequence of excessive T-lymphocytic infiltration, predominantly CD4+ T-cells, which are the main drivers of autoimmunological myocardial injury. Mörz described the expression of the vaccine-derived spike protein in the brain and the heart of a patient who developed multifocal necrotizing encephalitis upon vaccination with BNT162b2 (Mörz, 2022). Immunohistochemistry also revealed the expression of the vaccine-encoded spike protein in the vesicular keratinocytes and the endothelial cells in the dermis (Yamamoto et al., 2022).”
Despite having a long development pathway driven by the US Military DARPA in the ADEPT P3 Program announced in 2012, genetic vaccines have been poorly conceived by contractors without careful consideration of the biological ramifications of autoimmunity. To make matters worse, they were rushed through human clinical development by Operation Warp Speed and were too widely deployed, with 92% of the US population injected at least once according to the CDC. As a result, we have nearly the entire US population at risk for or with some subclinical manifestation of autoimmunity.
At this point, the best course is to remove the COVID-19 vaccines from human use as I have testified in the US Senate on December 7, 2022. The medical community needs to pick up the pieces with a giant research effort on vaccine injury pathophysiology with a major focus on autoimmunity.
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NO! NO! NO! You make it sound as if all this was a mistake or a misstep of honest vaccine development; a “misstep?” You’ve got a lot of the science correct by focusing on the proteins and immunity, but that’s it, almost like it’s intentional. The vaccines were developed to MURDER people, just the same as the so-called COVID Lab Leak; not a mistake or misstep! That’s complete BULLSHIT, doctor. Both the Virus and the Vaccines were Military Grade Weapons, not a god damn leak, and I can prove the media’s responses and reporting was also NOT a mistake, but Military Misinformation and Misdirection. I’m not a conspiracy theorist. I’ve researched ALL the scientific studies and doctors who’ve been complaining for decades about being stifled or destroyed for saying what I am now saying, what I have been saying for years. I know what I’m talking about. You are NOT doing all your homework, just part of it, or just enough so not to step on too many toes, or for whatever the reason…you are, in part, wrong about the who, what, when and why of it all. And I just don’t get it. You are too smart, and I just don’t’ get your half-way up the pyramid explanations, and you are not alone in doing this. Let me repeat: People are being Murdered by both Military Grade Bio-Weapons and Media coverage, and you are not helping by denying this bloody evil fact.
These mRNA and adenovirus vector quasi-vaccines are a menace, and their widespread, forced and deliberately misinformed use is part of the cluster of crimes against humanity which constitute the COVID-19 pandemic response https://nutritionmatters.substack.com/p/the-covid-19-pandemic-response-killed .
The majorities of whole professions acted together to ignore the vitamin D supplementation and other nutritional needs of the immune system and to deny access to a growing number of safe, effective, early treatments https://c19early.org which were inexpensive and well researched, in favour of patented, poorly researched, not very safe or effective antivirals and monoclonal antibodies which were vastly expensive.
Most people have only 1/10th to 1/2 of the circulating 25-hydroxyviitamin D their immune system needs to provide strong innate and adaptive responses to cancer cells, bacteria, fungi and viruses. For 70 kg 154 lb body weight, without obesity, about 0.125 mg 5000 IU vitamin D3 a day is required to attain these levels. Please read the research articles on vitamin D3 and the immune system at: https://vitamindstopscovid.info/00-evi/ . This includes a summary of Prof. Sunil Wimalawansa's bodyweight ratio vitamin D3 supplementation quantities, as ratios of body weight, with higher ratios for those suffering from obesity: https://www.mdpi.com/2072-6643/14/14/2997
The immune system needs at least 50 ng/mL 125 nmol/L circulating 25-hydroxyvitamin D (made, over days, in the liver from vitamin D3 cholecalciferol) to mount proper innate and adaptive responses, and to reduce the risk of wildly dysregulated inflammatory responses in response to infection, or to these quasi vaccines. The rest of this comment focuses on the primary reason for this excessive inflammation, which is made much worse by normal, very low (5 to 25 ng/mL) 25-hydroxvitamin D levels.
There is a vast set of health problems arising from excessive inflammation. Inflammation is an indiscriminate cell-destroying immune response which properly targets multicellular parasites such as helminths (intestinal worms). This is because the innate and adaptive (antibodies etc.) immune responses which target cancer cells, bacteria, fungi and viruses only work on individual cells or viruses. Since the eosinophils (the suicide bombers of the immune system) and other cells which mediate the inflammatory response kill all types of cells - our own and ideally those of the multicellular parasite - this is a potentially self-harming immune response which needs to be triggered only under the right circumstances and then be properly regulated.
For tens of millions of years, helminths have evolved compounds which they exude to downmodulate the inflammatory responses of their hosts. As best we know, all our ancestors, going back, many millions of years, and probably until the late 19th century or early 20th, were ubiquitously infested by one or more species of helminth. We have the immune system which our ancestors evolved to counter this pervasive down-modulation. So, in general, once we are de-wormed, humans (and our companion and agricultural animals) have overly-strong inflammatory responses to the point of being self-destructive - especially for some people whose genetic variation gives them even stronger than usual inflammatory responses.
This gives rise to a plethora of conditions including MS, rheumatoid arthritis, psoriasis, cluster headaches, migraine etc. Some people introduce relatively benign helminths to suppress these conditions: https://helminthictherapywiki.org.
Most people's typically low 25-hydroxyvitamin D levels, such as 5 to 25 ng/mL instead of the 50 ng/mL they really need (multiply by 2.5 to get nmol/L, as used by Australian and UK doctors) makes this excessive inflammation far worse, since immune cells such as Th1 regulatory lymphocytes cannot properly regulate these responses. See Chauss et al. 2021, cited and discussed at: https://vitamindstopscovid.info/00-evi/#chauss .
For reasons which are not properly understood, much higher than 50 ng/mL 25-hydroxyvitamin D levels (under medical supervision) can strongly suppress all these auto-immune inflammatory disorders, including especially MS - which most doctors believe is incurable. See the Coimbra protocols and research articles cited at: https://vitamindstopscovid.info/06-adv/ .