The Covid Vaxxes and Pathological Priming By Brian Simpson
Pathological priming is not something out of a Hollywood zombie movie, but the phenomenon where, organisms are exposed to epitopes that match human proteins, leading to the production of autoreactogenic antibodies that attack tissues anywhere in the body. It is hypothesed that the Covid vaccines could lead to pathological priming based upon the evidence of increased all-cause mortality, seen in a number of jurisdictions, particularly in the UK, and histopathological evidence of autoimmunity across various organs. More bad news.
“A compilation of evidence is disturbing. Further mass casualities might be preventable.
Pathogenic priming, as originally described, is the act of exposing people (or animals) to epitopes that match human proteins, leading to the inducement of autoreactogenic antibodies that attack tissues anywhere in the body. I described pathogenic priming in April, 2020 and predicted that tissues across the body could become afflicted due to exposure to COVID-19 proteins.
Evidence is mounting that points to pathogenic priming contributing morbidity and mortality among the vaccinated, including
- Increased all-cause mortality
- Histopathological evidence of autoimmunity across various organs.
An important message, with data, came to me today on one of my many email threads. I am sharing this on Popular Rationalism with permission Ronald Kostoff, who fowarded the analysis below:
A German pathologist performed autopsies on fifteen post-inoculation patients who died, and found that >90% had their organs attacked by their immune systems (autoimmunity). The following video describes the main results (https://www.bitchute.com/video/fHIT55iM4Zv9/ ), and a written summary follows ( https://doctors4covidethics.org/wp-content/uploads/2021/12/end-covax.pdf). The full 4 hr symposium that was live-streamed on December 10th, 2021 and that contains this and other valuable information can be found here Gold Standard Covid Science in Practice: Interdisciplinary Symposium II, December 10, 2021 – Doctors for COVID Ethics (doctors4covidethics.org).
Commenting on the above, Ronald wrote: "If the autopsy findings are confirmed by other pathologists with additional samples, and if they are combined with the findings of Dr. Hoffe (>60% inoculant recipients have elevated D-dimer tests and evidence of clotting) and Dr. Cole (increase in cancers after inoculation, including twenty-fold increase in uterine cancer), we are seeing a disaster of unimaginable proportions. The conclusion (if supported by further data) is that essentially EVERY inoculant recipient suffers damage, with more damage after each shot. The damage could be cumulative, and the shots may be synergistic. Given the seriousness of the types of damage (autoimmune diseases, cancer, re-emergent dormant infections, clotting/strokes, cardiac damage, etc.), these effects will translate into lifespan reduction, which should be counted as deaths from the inoculations. So, in the USA, where ~200M people have been fully inoculated, the number of deaths will not be the 10,000 or so reported in VAERS, or 500,000-1,000,000 scaled-up deaths from VAERS, but could be closer to tens of millions (or more) when the inoculation effects play out!
What the above three findings (Burkhart, Hoffe, Cole, and I suspect many others who have not yet come forward) show is that the post-inoculation effects are not rare events (as reported by the media-gov't), but are in actuality frequent events. They may be, in fact, universal, with different degrees of severity and damage for each recipient. The question is whether it is possible to reverse these inoculation-based adverse events. Can the innate immune system be fully restored? Can the microclotting be reversed? Can the autoimmunity be reversed? There is a wide spectrum of opinions on whether this is possible, none of which is overly convincing. Are we headed for the situation where the ~30% unvaxxed will be devoting their lives to operating whatever is left of the economic infrastructure and serving as caretakers for the vaxxed?
The above sounds extreme, and maybe when more data are gathered from myriad credible sources the results and conclusions may change, but right now the above data seem to synchronize with the demonstrated underlying mechanisms of damage. Additionally, we seem to be doubling down on inoculations, with fourth booster being proposed for Israel, and UK suggesting quarterly boosters."
The full original message is as follows:
“15 patients who died days to 6 months after the shots were cleared of the cause of deaths as from the shots by a coroner because the macroscopic appearance of the organs was overall unremarkable.
Then a pathologist spends 6 months to examine the patients, and histopathological studies found that 92% had their organs attacked by their immune system (autoimmune attack)
Dr. Bhakdi’s 15 min video about these findings are here:
https://www.bitchute.com/video/fHIT55iM4Zv9/
(Most important parts are from 1:20 to 3:00.)
A written summary of Dr. Bhakdi’s and Dr. Burkhardt’s presentations at the Doctors for COVID Ethics symposium can be found here https://doctors4covidethics.org/wp-content/uploads/2021/12/end-covax.pdf
[The full 4 hr symposium that was live-streamed on December 10th, 2021. can be found here Gold Standard Covid Science in Practice: Interdisciplinary Symposium II, December 10, 2021 – Doctors for COVID Ethics (doctors4covidethics.org)]
Summary of Bhakdi's and Burkhardt's Pathology Findings:
Why the vaccines cannot protect against infection and trigger autoimmunity
There are functional distinctions between the two major categories of antibodies which the body produces in order to protect itself from pathogenic microbes. The first category (secretory IgA) is produced by immune cells (lymphocytes) which are located directly underneath the mucous membranes that line the respiratory and intestinal tract. The antibodies produced by these lymphocytes are secreted through and to the surface of the mucous membranes. 1 These antibodies are thus on site to meet air-borne viruses, and they may be able to prevent viral binding and infection of the cells. The second category of antibodies (IgG and circulating IgA) occur in the bloodstream. These antibodies protect the internal organs of the body from infectious agents that try to spread via the bloodstream. Vaccines that are injected into the muscle – i.e., the interior of the body – will only induce IgG and circulating IgA, not secretory IgA. Such antibodies cannot and will not effectively protect the mucous membranes from infection by SARS-CoV-2. Thus, the currently observed “breakthrough infections” among vaccinated individuals merely confirm the fundamental design flaws of the vaccines. Measurements of antibodies in the blood can never yield any information on the true status of immunity against infection of the respiratory tract. The inability of vaccine-induced antibodies to prevent coronavirus infections has been reported in recent scientific publications. The vaccines can trigger self-destruction. A natural infection with SARS-CoV-2 (coronavirus) will in most individuals remain localized to the respiratory tract. In contrast, the vaccines cause cells deep inside our body to express the viral spike protein, which they were never meant to do by nature. Any cell which expresses this foreign antigen will come under attack by the immune system, which will involve both IgG antibodies and cytotoxic T lymphocytes. This may occur in any organ. We are seeing now that the heart is affected in many young people, leading to myocarditis or even sudden cardiac arrest and death. How and why such tragedies might causally be linked to vaccination has remained a matter of conjecture because scientific evidence has been lacking. This situation has now been rectified in histopathologic studies..
Histopathologic studies: the patients
Most frequently afflicted were the heart (14 of 15 cases) and the lung (13 of 15 cases). Pathologic alterations were furthermore observed in the liver (2 cases), thyroid gland (Hashimoto’s thyroiditis, 2 cases), salivary glands (Sjögren`s Syndrome; 2 cases) and brain (2 cases).
A number of salient aspects dominated in all affected tissues of all cases:
- Inflammatory events in small blood vessels (endothelitis), characterized by an abundance of T lymphocytes and sequestered, dead endothelial cells within the vessel lumen;
- The extensive perivascular accumulation of T-lymphocytes;
- A massive lymphocytic infiltration of surrounding non-lymphatic organs or tissue with T lymphocytes.
Lymphocytic infiltration occasionally occurred in combination with intense lymphocytic activation and follicle formation. Where these were present, they were usually accompanied by tissue destruction. This combination of multifocal, T-lymphocyte-dominated pathology that clearly reflects the process of immunological self-attack is without precedent. Because vaccination was the single common denominator between all cases, there can be no doubt that it was the trigger of self-destruction in these deceased individuals.
Conclusion
Histopathologic analysis show clear evidence of vaccine-induced autoimmune-like pathology in multiple organs. That myriad adverse events deriving from such auto-attack processes must be expected to very frequently occur in all individuals, particularly following booster injections, is self evident. Beyond any doubt, injection of gene-based COVID-19 vaccines places lives under threat of illness and death. We note that both mRNA and vector-based vaccines are represented among these cases, as are all four major manufacturers.
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