A couple of issues ago, I wrote about something called ADE or Antibody-dependent Enhancement. Children’s Hospital of Philadelphia explains that “ADE occurs when the antibodies generated during an immune response recognize and bind to a pathogen, but they are unable to prevent infection. Instead, these antibodies act as a ‘Trojan horse,’ allowing the pathogen to get into cells and exacerbate the immune response.”[i] A study published in September of 2020 concludes: “Data from the study of SARS-CoV and other respiratory viruses suggest that anti-SARS-CoV-2 antibodies could exacerbate COVID-19 through antibody-dependent enhancement (ADE). Previous respiratory syncytial virus and dengue virus vaccine studies revealed human clinical safety risks related to ADE, resulting in failed vaccine trials.”[ii]
Understand that the National Institute of Health argues that ADE should not pose such a risk “because coronavirus diseases in humans lack the clinical, epidemiological, biological, or pathological attributes of ADE disease exemplified by dengue viruses (DENV). In contrast to DENV, SARS and MERS CoVs predominantly infect respiratory epithelium, not macrophages.”[iii] (Got that?) Children’s Hospital of Philadelphia takes the same view.
This however is not a unanimous view. Here’s the alternate view. The antibodies produced by a natural COVID infection is different from one produced by the vaccines. Karl Denninger, writing in Market Ticker explains. “Coronaviruses are notorious for ADE reactions, where antibody presence potentiates the infection instead of protecting against it… The poster child for ADE in coronaviruses was an attempted vaccine for a feline coronavirus that often made cats very sick. The vaccine killed every one of them in the test when they were later exposed, wildly potentiating the infection….NOT ONE VACCINATED CAT SURVIVED A CHALLENGE WITH THE ACTUAL VIRUS.” A mutated version of the virus could selectively target “ADE in people with the specific antibodies from vaccination, which are distinct from natural infection, could easily kill every single person who was vaccinated and not harm or only make mildly sick those who either had Covid 19 naturally or who were uninfected and unvaccinated.” [iv]
Dr Sherri Tenpenny weighs in on the subject. She is “an osteopathic medical doctor, board certified in three medical specialties. Widely regarded as the most knowledgeable and outspoken physician on the adverse impact that vaccines can have on health.” [For further biographical info click the link.] Dr Tenpenny sees the human race as the guinea pigs in this vaccine rollout. She warns that in about 3 to 6 months, many who have taken the vaccine will get sick and a good number of those will die.
Specifically of the AstraZeneca vaccine she writes: “This vaccine candidate is of interest because the clinical studies, done in collaboration with the University of Oxford, were widely publicized as the first and most promising vaccine,” she wrote. “However, in May 2020, it was reported that all the vaccinated monkeys treated with the Oxford vaccine became infected when challenged. Then, why did the company press forward with the renamed, AZD1222 vaccine candidate? Because even though the vaccine did not protect the animals from infection, it did moderate the disease. Watch for this type of logic as the 80+ COVID vaccines try to make their way into the multi-trillion-dollar vaccine market.”
Then there is the little matter of a much-referenced study of a Coronavirus vaccine in animals. As Tim Brown points out in The Washington Standard, “In a 2012 study of mice, ferrets, hamsters, and Cynomolgus monkeys, using various coronavirus proteins and various adjuvants, researchers reported immunopathology in every animal that had been vaccinated and then re-exposed to a SARS-CoV virus.” In some studies all the animals died post vaccine after encountering the virus in the wild.
Researchers argued that human tests showed that the vaccines showed “antibody response” and were determined to be “safe.” That was only in the short term. However, the animal trials producing immunopathology pointed to “hypersensitivity to SARS-CoV components.” They concluded that caution should be used in rolling out the vaccines to humans. Of course, that’s not what happened with this emergency rollout that saw effective treatments like Hydroxychloroquine and Ivermectin suppressed so that vaccines could be developed for hundreds of billions in profits.[v]
The center of the ADE issue centers on the long-term effects of the vaccines. Besides the fact that the mRNA versions of the vaccine can potentially and permanently affect your DNA, there is the matter of your immune system turning on you. According to Dr Tenpenny, the artificial antibodies produced by the vaccine are hanging out in your body essentially dormant until they encounter a “garden variety Coronavirus” – there are 36 of them – and that’s what sets the process in motion. “The antibody to the spike protein is going to destroy your lungs. The antibody to the spike protein is going to shut off your M2 anti-inflammatory microphages. And the antibody to the spike protein is going to loosely bind that virus, or loosely bind that messenger RNA and drag it inside of your cell like a Trojan Horse phenomenon make it start replicating and have this process go on and on and on.”[vi] Well, there’s the story from both sides. Now, which to believe! As for me: I’ll err on the side of caution.
[i] https://www.chop.edu/centers-programs/vaccine-education-center/vaccine-safety/antibody-dependent-enhancement-and-vaccines,
Viewed February 17, 2021
[ii]Lee, W.S., Wheatley, A.K., Kent, S.J. et al. Antibody-dependent enhancement and SARS-CoV-2 vaccines and therapies.
Nat Microbiol 5, 1185–1191 (2020). https://doi.org/10.1038/s41564-020-00789-5, – Nature.com
[iii] Scott B Halstead, Leah Katzelnick, COVID-19 Vaccines: Should We Fear ADE?, National Library of Medicine,
National Institute of Health, November 13, 2020
[iv] Karl Demminger, The West’s Obituary, Market Ticker, February 13, 2021
[v] Tim Brown, Dr. Sherri Tenpenny: How The Depopulation COVID Vaccines Will Start Working In 3-6 Months, Washington Standard,
February 11, 2021
[vi] CV-19 SHOT WITH DR. TENPENNY AND REINETTE SENUM – MORE FATALITIES IN 3-6 MONTHS, Bitchute,
February 13, 2021
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