March 24th, 2021

Why Will Many More People Die From mRNA Vaccines?

INTRODUCTION
I have posted three articles in recent weeks about the immediate side effects of mRNA vaccines:
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Dr Tenpenny Explains A Serious & Potentially Deadly Side Effect Of mRMA Vaccines (1)
Some Side Effects Are Not A Coincidence: mRNA COVID-19 Vaccines Cause Lymphadenopathy (2)
mRNA Vaccines Create An Autoimmune Response Causing Thrombocytopenia, Bleeding And Blood Clots (3)
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In this article I will explore the more long term consequences of these medications.
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HOW WE KNOW MRNA VACCINES ARE NOT SAFE?
We have been told over and over that mRNA vaccines are safe. It may be hard to believe, but there is ample evidence that they are not safe at all. This issue is discussed by Prof Delores Cahill in the video interview below. While I have investigated some of the immediate consequences of mRNA vaccination, Prof Cahill concentrates on is the long-term consequences of these injections. You should realize that Prof. Cahill was recently dismissed from her academic post at University College Dublin, and this video cannot be posted on Twitter at its original location on ButChute.(4)
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Lawyer Dr. Reiner Fuellmich, Prof. Delores Cahill, Lawyer Viviane Fischer Questioning mRNA Vaccine
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How can we know what the long-term consequences of the mRNA vaccines are if they are new, and have never been used on humans before? We can know because over a decade ago they were tested on a range of animals in an effort to develop a vaccine for SARS. This video is one of many discussions of the consequences of injecting animals – mice and ferrets – with gene derived “vaccines” like those being used today.
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In the animal studies, the animals were first vaccinated against SARS. Then at a later time they were presented with a real world SARS virus. This initiated a clotting immunopathology in the lungs and they all died. Prof Cahill explains that the same thing can happen with SARS or Covid-19 in a different order. If you have already come into contact with Covid-19, your immune system will already be primed to attack it if it appears again. If you are then vaccinated with the mNRA vaccine, the spike protein from the Covid-19 virus will be generated in many places in your body by the immune system. (This is how the vaccine works.) These presentations will then be attacked by your primed immune system, so your immune system will be attacking itself. This is what an antoimmune disease consists of, and it will produce the same clotting immunopathology in the lungs.
If you want to have a deeper understanding of the biology involved in this I need to reproduce part of an earlier article which explains how mRNA vaccines work and how this sets up an autoimmune response in humans and other animals.
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HOW AN mRNA VACCINE WORKS
We must begin with a description of how an mRNA vaccine works. This account is taken from a website of the Center for Disease Control, the CDC.
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"COVID-19 mRNA vaccines give instructions for our cells to make a harmless piece of what is called the “spike protein.” The spike protein is found on the surface of the virus that causes COVID-19.
COVID-19 mRNA vaccines are given in the upper arm muscle. Once the instructions (mRNA) are inside the immune cells, the cells use them to make the protein piece. After the protein piece is made, the cell breaks down the instructions and gets rid of them.
"Next, the cell displays the protein piece on its surface. Our immune systems recognize that the protein doesn’t belong there and begin building an immune response and making antibodies, like what happens in natural infection against COVID-19.
"At the end of the process, our bodies have learned how to protect against future infection. The benefit of mRNA vaccines, like all vaccines, is those vaccinated gain this protection without ever having to risk the serious consequences of getting sick with COVID-19."(5)
IMAGE FROM WIKIPEDIA(6)
The “immune cells” in the description above are known as Dendritic cells. "Their main function is to process antigen material and present it on the cell surface to the T cells of the immune system."(7) Other cells in the body "can potentially absorb vaccine mRNA, manufacture spikes, and display spikes on their surfaces, however dendritic cells absorb the mRNA globules much more avidly."(8)
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"Once the viral antigens are produced by the host cell, the normal adaptive immune system processes are followed. Antigens are broken down by proteasomes, then class I and class II MHC molecules attach to the antigen and transport it to the cellular membrane, 'activating' the dendritic cell. Once the dendritic cells are activated, they migrate to lymph nodes, where the antigen is presented to T cells and B cells.This eventually leads to the production of antibodies that are specifically targeted to the antigen, resulting in immunity."(9)
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HOW mRNA VACCINES CAUSES AN AUTOIMMUNE RESPONSE
This is the first comment on mRNA vaccines in a letter the doctyors4covidethics sent to the European Medicines Agency.(10)
“1. Following intramuscular injection, it must be expected that the gene-based vaccines will reach the bloodstream and disseminate throughout the body [1].”
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This is the third comment:
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“3. It must be expected that during expression of the vaccines’ nucleic acids, peptides derived from the spike protein will be presented via the MHC I — pathway at the luminal surface of the cells. Many healthy individuals have CD8-lymphocytes that recognize such peptides, which may be due to prior COVID infection, but also to cross-reactions with other types of Coronavirus.[3; 4] [5]. We must assume that these lymphocytes will mount an attack on the respective cells.”
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In the account given by the CDC, the nanoparticles in the vaccine will enter and be processed by the dendritic cells. Then the “cell displays the protein piece [it has created from the nanoparticle] on its surface. Our immune systems recognize that the protein doesn’t belong there and begins building an immune response and making antibodies...” A passage from Wikipedia explains this process as follows: “Once the dendritic cells are activated, they migrate to lymph nodes, where the antigen is presented to T cells and B cells.”(11)
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But the doctors4covidethics explain that many people will have been exposed to COVID or other types of Coronavirus. This means that the “spike” protein (made up of long chains of amino acids) which occurs on all coronavirus or peptides (smaller chains of amino acids) which are parts of the spike protein, will be recognized as belonging to a pathogen. Thus when the dendritic cell displays “the protein piece” created from the vaccine’s nanoparticle the immune system will not “begin to build an immune response and make antibodies...” or just “migrate to the lymph nodes”. Instead, since the dendritic cell displays a protein piece created from the vaccine nanoparticle, it will be attacked by the CD8-lymphocytes that recognize such peptides as pathogens.
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We can see that in the story the CDC tells assumes nobody has been exposed to COVID or any other types of Coronavirus. They assume the immune system is ignorant of the threat of COVID, and the mRNA vaccine is going to teach the immune system to be prepared to attack it. But introducing the spike protein will not "teach" the immune system anything if a person has had some previous exposure to any type of Coronavirus. The cell which displays the recreated spike protein will be attacked because it has already been recognized as a pathogen and the immune system via the CD8-lymphocytes will destroy it. So what’s going on in the lymph nodes? There is a hyperimmune reaction to chronic antigenic stimuation, autoimmune activity, and the secretion of large amounts of antibodies.
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PRIOR KNOWLEDGE OF THE DANGER OF MRNA VACCINES
In this section I will present just a few comments which highlight the dangers of mRNA vaccines based on the earlier experimentation. This is a report of what happened in the original experiments ca. 2009:
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“In SARS, a type of ‘priming’ of the immune system was observed during animal studies of SARS spike protein-based vaccines leading to increased morbidity and mortality in vaccinated animals who were subsequently exposed to wild SARS virus. The problem, highlighted in two studies, became obvious following post-vaccination challenge with the SARS virus found that recombinant SARS spike-protein-based vaccines not only failed to provide protection from SARS-CoV infection, but also that the mice experienced increased immunopathology with eosinophilic infiltrates in their lungs. Similarly, found that ferrets previously vaccinated against SARS-CoV also developed a strong inflammatory response in liver tissue (hepatitis). Both studies suspected a ‘cellular immune response’.”(12)
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This cellular immune response has several descriptions in the scientific literature: viral interference, Antibody Dependent Enhancement (ADE), Pathogenic priming, vaccine associated disease enhancement (VADE), or autoimmune reactions overloading the immune system. This is how one biologist explains it:
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“The ADE (Antibody Dependent Enhascement) mechanism is quite complex but can be summarized as follows: when a subject who possesses a sub-optimal antibody level (as a result of primary infection or vaccination) comes into contact with a similar virus and becomes infected, his immune system promotes infection and fatal complications of the disease. In other words, a proportion of the vaccinated are predisposed by the vaccination to developing serious and fatal complications of the very disease they are meant to be protected from.”(13)
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Now consider this passage from Wikipedia:
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“ADE [or cellular immune response] may cause enhanced respiratory disease and acute lung injury after respiratory virus infection with symptoms of monocytic infiltration and an excess of eosinophils in respiratory tract. ADE along with type 2 T helper cell-dependent mechanisms may contribute to a development of the vaccine associated disease enhancement (VADE), which is not limited to respiratory disease. Some vaccine candidates that targeted coronaviruses, RSV virus and Dengue virus elicited VADE, and were terminated from further development or became approved for use only for patients who have had those viruses before.”(14)
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While this passage makes it quite clear that vaccines aimed at coronaviruses (namely the mRNA Covid-19 vaccines) “may cause enhanced respiratory disease and acute lung injury after respiratory virus infection”, at the end of the article under the heading “Misinformation related to the COVID-19 pandemic” we find this:
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“ADE has been observed in animal studies during the development of coronavirus vaccines, but as of 14 December 2020 there had been no observed incidences in human vaccine trials. Anti-vaccination activists cite ADE as a reason to avoid vaccination against COVID-19, but the expectation is that ADE would have already been observed in human trials if it were a risk. "Overall, while ADE is a theoretical possibility with a COVID-19 vaccine, clinical trials in people so far have not shown that participants who received the vaccine have a higher rate of severe illness compared to participants who did not receive the vaccine.”(15)
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Note the date: 14 December 2020. There had been few if any vaccinated humans at that point. As I explained above, evidence of such reactions has been found, but you won’t find it in Wikipedia.
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WHAT WENT WRONG?
Why did companies and regulators  develop and release mRNA vaccines given this well-known problem? Some people warned of the dangers as follows:
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“Challenge of mice given any of the vaccines led to occurrence of Th2-type immunopathology suggesting hypersensitivity to SARS-CoV components was induced. Caution in proceeding to application of a SARS-CoV vaccine in humans is indicated.”(16)
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You may have your own answer to this qustion, but mine is simply that they did not want a “safe” vaccine. They wanted one that would kill people and thereby “solve” the “overpopulation” problem. I think this is shown by the fact that they are covering up the immediate consequences of vaccination, they refuse to allow autopsies, and while they talk about “safety” they are not really interested in the deaths and injuries which have resulted.
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Careful observers are aware that Covid-19 is not a health problem. Covid-19 is a viral infection that governments have used to justify removing all basic freedoms on the grounds of a medical “emergency”. Covid-19 is not about health but control, and it may also be about killing off part of the world’s population with medications that are supposed to “Save Lives”.
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FOOTNOTES
10. "Urgent Open Letter from Doctors and Scientists to the European Medicines Agency regarding COVID-19 Vaccine Safety Concerns”; https://doctors4covidethics.medium.com/urgent-open-letter-from-doctors-and-scientists-to-the-european-medicines-agency-regarding-covid-19-f6e17c311595
12. James Lyons-Weiler, "Pathogenic priming likely contributes to serious and critical illness and mortality in COVID-19 via autoimmunity"; https://www.sciencedirect.com/science/article/pii/S2589909020300186
13. Dr.SSA Loretta Blogan, "mRNA VACCINE INDUCED DAMAGE MECHANISMS", Pdf here: https://drive.google.com/file/d/1Vol-S4Ac5Ws83zv1FYa5FGfgOCUH402_/view
15. Ibid.
16. Chien-Te Tseng and others, "Immunization with SARS coronavirus vaccines leads to pulmonary immunopathology on challenge with the SARS virus", https://pubmed.ncbi.nlm.nih.gov/22536382/
If you want to look at more scientitific literature on this subject download the Pdf by Dr.SSA Loretta Blogan, “mRNA VACCINE INDUCED DAMAGE MECHANISMS”.