{"id":66690,"date":"2021-05-26T10:30:48","date_gmt":"2021-05-26T14:30:48","guid":{"rendered":"http:\/\/stateofthenation.co\/?p=66690"},"modified":"2021-05-26T10:32:41","modified_gmt":"2021-05-26T14:32:41","slug":"these-are-some-of-the-mechanisms-for-covid-vaccine-induced-deaths-and-injuries","status":"publish","type":"post","link":"http:\/\/stateofthenation.co\/?p=66690","title":{"rendered":"These are some of the mechanisms for Covid vaccine-induced deaths and injuries<\/b>"},"content":{"rendered":"

Mechanisms of COVID-19 Vaccine Induced Injuries\/Deaths<\/h1>\n

By Maggie Zhou, PhD<\/p>\n

Update 3<\/strong>: A peer reviewed paper<\/a> from MIT published in Apr 2021,[20] confirmed their earlier pre-print version<\/a> published Dec13, 2020,[21] that \u201cReverse-transcribed SARS-CoV-2 RNA can integrate into the genome of cultured human cells and can be expressed in patient-derived tissues\u201d.\u00a0 Their results are \u201cconsistent with a LINE1 retrotransposon mediated, target-primed reverse transcription and retroposition mechanism.\u201d\u00a0 Even though with infection of SARS-CoV-2virus, they detected only subgenomic sequences derived mainly from the 3\u2032 end of the viral genome integrated into the DNA of the host cell,in the case of mRNA vaccines, given that we\u2019re told the S protein gene is the only gene encoded by the mRNA, which by default is near the 3\u2019 end<\/strong>, and was given a poly(A) tail and various other features to stabilize it, and given that tens of billions of copies of this mRNA are injected in one dose, it seems to me that there\u2019s a good chance similar reverse transcription and retrotransposition of the S protein gene – the MOST PATHOGENIC gene of this entire virus – could really occur, as many scientists have warned from the beginning.\u00a0 Once integrated into the genome, the host could express the S protein in the long term, which would trigger persistent autoimmune response<\/strong>, causing attack on the cells it has integrated into.<\/p>\n

Update 2:\u00a0 <\/strong>Here’s yet another way that making our own cells express the spike protein via the genetic vaccines can lead to disaster: causing cells expressing the spike protein and cells that have ACE2 receptor on their surface to conglomerate, forming something called a “multinucleated syncytia”:<\/p>\n

“Proteins that mediate fusion between viral and cellular membranes can in some cases also do so between cells that express the viral fusion protein and those that express the viral receptor. For instance, cells expressing the HIV-1 envelope glycoprotein gp160 can form multinucleated syncytia with cells expressing the HIV-1 receptors CD4 and CCR5”. The 2003 Nature paper went on to demonstrate that “293T cells transfected with ACE2, but not those transfected with human immunodeficiency virus-1 receptors, formed multinucleated syncytia with cells expressing S protein (of SARS-CoV-1)”.[19<\/a>]<\/p>\n

UPDATE: I’ve expanded the second half of the article to include many more mechanisms that I’m aware of but didn’t include in the original version.<\/strong><\/p>\n

\"\"<\/a><\/p>\n

A study<\/a> on UK government\u2019s website, dated Apr 2021, conducted by the\u00a0ISARIC4C<\/a>\u00a0consortium, found<\/a> that among the hospitalized COVID patients who had ALREADY BEEN VACCINATED, the onset of symptoms is most commonly from the day of vaccination to 3 days after that. \u00a0The onset is 5x as frequent ON the day of the vaccination as the day BEFORE vaccination! [1]<\/p>\n

The preferred mainstream explanation is blaming behavioural change \u2013 they assume that those who had been vaccinated shielded & isolated less.\u00a0 Yet they have no evidence to back that up.\u00a0 Crucially, \u201cNo one is suggesting there was a change of behaviour within care homes, except for inviting people in to carry out the vaccinations. However, care homes in every corner of the country saw outbreaks from December\u201d, wrote a rebuttal published in the British Medical Journal<\/a>.[2]<\/p>\n

The other idea offered by some mainstream academics is that going to the vaccination centers itself may be a \u201csuper-spreader event\u201d – but again, care homes didn\u2019t fit that bill.<\/p>\n

Also, even if these people did contract the virus on the vaccination day, why would more of them have symptom onset on that day and the 3 days immediately after, rather than the usual incubation period of 5 days?<\/p>\n

\n

FAR MORE LIKELY are the following mutually non-exclusive mechanisms:<\/p>\n

    \n
  1. The rebuttal in the BMJ<\/a> mentioned above[2] pointed out that both Pfizer and AstraZeneca\u2019s trials had shown white blood cell depletion<\/strong> in the first 3 days post vaccination.\u00a0 The phenomenon is known for other vaccines as well, and there\u2019s at least evidence in children<\/a> that such transient white cell depletion results in susceptibility to viral infections.[3]\u00a0 In this scenario, an infection previously kept in check by the immune system could become active when response to the vaccine depleted circulating white blood cells.<\/li>\n
  2. The mRNA and DNA vaccines use nanoparticles to enclose the nucleic acids.\u00a0 There has been an accumulating number of studies that found that various types of nanoparticles<\/strong> can interferewith the function of our blood cells, and with the coagulation system, shifting the hemostatic balance, causing deep vein thrombosis (DVT) and disseminated intravascular coagulopathy (DIC), among other serious complications.[8,9]\u00a0 Also, the mRNA vaccine nanoparticles contain PEG-lipid<\/strong>, and the the DNA vaccine nanoparticles contain polysorbate 80<\/strong>, both have been known to be allergenic and found responsible for anaphylactic reactions in the past.[10]<\/li>\n
  3. The spike protein of SARS-CoV-2 alone<\/strong>, introduced intratracheally, as well as in in vitro<\/em> experiments, has been shown to damage lung vascular endothelial cells<\/strong> by downregulating ACE2, and consequently inhibiting mitochondrial function<\/strong>, triggering reactive oxygen species production, increasing glycolysis, and extracellular acidification.[11,4]<\/li>\n
  4. On Dec 9, 2020, BEFORE vaccination rollouts in most countries, Dr. J. Patrick Whelan MD PhD, formerly warned the FDA<\/a> that, according to multiple lines of evidence, vaccines using SARS-CoV-2 spike protein (including mRNA and DNA vector vaccines) may cause microvascular injury to distant organs including the brain, heart, liver, and kidneys.[5]<\/li>\n<\/ol>\n

    He cited evidence that while \u201cthe coronavirus replicates almost exclusively in the septal capillary endothelial cells of the lungs and the nasopharynx\u201d, \u201cviral lysis and immune destruction of those cells releases viral capsid proteins (or pseudovirions) that travel through the circulation and bind to ACE2 receptors in these other parts of the body\u2026\u2026 that not only damages the microvascular endothelium but also induces the production of many pro-inflammatory cytokines\u201d.\u00a0 He cited evidence that the brain tissues of those that died from COVID were found to have pseudovirions (spike, envelope, and membrane proteins) without viral RNA, in the endothelia of cerebral microvessels, and that injecting just the S1 spike subunit in mice led to neurologic signs.[5]<\/p>\n

      \n
    1. On Jan 26, 2021, Dr. Hooman Noorchashm emailed the FDA regulators, Pfizer leaders and the press, to deliver \u201ca warning and a, nearly certain, prognostication\u201d<\/a>, that anyone who has had a recent COVID infection<\/strong> (irrespective of whether they are symptomatic or convalescent) can be expected to have viral antigens in the endothelial lining of their blood vessels, and that vaccine triggered antigen specific immune response will target those antigens, and therefore those tissues, and cause tissue inflammation and damage.[6]\u00a0 In other words, the vaccines will cause vasculature damage and blood clots in the lungs, as well as damage in the vasculature of the brain, heart, liver, kidney etc., anywhere residual viral antigens from a recent infection may be found.<\/li>\n<\/ol>\n

      It’s relevant with regard to what Dr. Noorchashm is warning about, to note that Pfizer’s clinical trial protocol<\/a> (on page 41) explicitly excluded<\/strong> anyone who has had COVID-19 from enrolment.[7]<\/p>\n

        \n
      1. Another point specifically about the mRNA and DNA vaccines encoding the spike protein, is raised by Dr. Sucharit Bhakdi, who was for over 2 decades the head of the Institute of Medical Microbiology and Hygiene, University of Mainz, and Editor in Chief of Medical Microbiology and Immunology.<\/li>\n<\/ol>\n

        He warned<\/a> that a large part of the injected mRNA or DNA-containing nanoparticle packets encoding the spike protein will reach local lymph nodes<\/strong>, and through there, into blood circulation<\/strong>.\u00a0 In the lymph nodes, when they\u2019re taken up by lymphocytes which then express the spike protein, those cells will be targeted for destruction by other lymphocytes, (likely accounting for the white blood cell depletion mentioned in #1 above). \u00a0The lymphocytes thus activated will multiply and swarm out of the lymph nodes to seek out more S protein antigen.\u00a0 They\u2019ll attack any muscle cells where the S protein is presented (muscle swelling, pain).[12]<\/p>\n

        The nanoparticles that get into the bloodstream will be trapped<\/strong> there.\u00a0 Some will fuse with blood cells, but most will be taken up by endothelial cell lining the smallest of veins<\/strong> where blood flows really slow.\u00a0 The expression and presentation of the S protein by these microvascular endothelial cells attracts and activates platelets<\/strong>, which induces clotting. \u00a0These cells also produce trash during spike protein production, which he says will be placed outside the cell, and attractskiller lymphocytes<\/strong> to attack the presenting endothelial cells, damaging the vascular lining, causing inflammation, and clotting.[12]<\/p>\n

          \n
        1. Many have been pointing out from the beginning, the very real danger of Antibody Dependent Enhancement of Disease (ADE)<\/strong>, that any SARS-CoV-2 vaccine may cause.\u00a0 All attempts to develop a vaccine against the closest human coronavirus, SARS-CoV, had failed in the past two decades, when vaccinated animal models got more severe disease and died, upon challenge with the actual virus.\u00a0 All SARS-CoV-2 vaccines clinical trials have simply not had enough observation time to allow such a deadly consequence to become apparent, before the vaccine rollouts were rushed worldwide \u2013 and we\u2019re already seeing the beginning of the onslaught! [13-15]<\/li>\n
        2. The SARS-CoV-2 spike protein has also been found to contain high sequence similarity to 4 human proteins essential for embryonic development<\/strong>, including Syncytin-1 and Syncytin-2, since February 2020.[16]\u00a0 This lead Dr. Wolfgang Wodarg and Dr. Michael Yeadon (Pfizer’s former chief scientific officer) to write an urgent petition on Dec 1, 2020, to the European Medicines Agency, to halt the vaccine rollout due to the possibility that antibodies against the S protein in vaccinated women may attack these proteins, preventing the formation of a placenta, and rendering them infertile<\/strong>.[17]\u00a0 Like all the other warnings, it was completely ignored.<\/li>\n
        3. Yet another treachery with the spike protein is its potential ability to cause prion disease, both by the protein, and by the mRNA for it contained in Pfizer and Moderna vaccines.\u00a0 I will make a separate post of this.<\/li>\n
        4. As if all that isn\u2019t bad enough, some scientists (e.g., Dr. Judy Mikovits) have stated that vaccinated people may shed microRNAs (miRNA)<\/strong> derived from the genetic vaccines, which could explain the many adverse health effects that unvaccinated people around those vaccinated are reporting (especially many women reporting abnormal and extremely heavy menses, even spontaneous abortions).\u00a0 She says these miRNAs can spread through air, and easily taken in by another person, as she’s worked on formulating therapeutic miRNA for aerosolized delivery.[18]<\/li>\n<\/ol>\n

          So indeed, the spike protein that the vaccines contain or encode for, is alone sufficient to cause COVID symptoms (and deaths in severe cases), and have numerous medium to long term potential serious consequences.\u00a0 Only criminal governments would have rushed it ahead and imposed it on the world with utter deceit.<\/p>\n

          \n

          [1] https:\/\/lockdownsceptics.org\/2021\/05\/01\/major-study-finds-abundance-of-patients-admitted-to-hospital-with-covid-within-seven-days-of-vaccination\/<\/a><\/p>\n

          https:\/\/assets.publishing.service.gov.uk\/government\/uploads\/system\/uploads\/attachment_data\/file\/982499\/S1208_CO-CIN_report_on_impact_of_vaccination_Apr_21.pdf<\/a><\/p>\n

          [2] https:\/\/www.bmj.com\/content\/372\/bmj.n783\/rr<\/a><\/p>\n

          [3] https:\/\/pubmed.ncbi.nlm.nih.gov\/29525279\/<\/a><\/p>\n

          [4] https:\/\/medicalxpress.com\/news\/2021-04-sars-cov-spike-protein-lung.html<\/a><\/p>\n

          https:\/\/www.eventscribe.net\/2021\/EB2021\/index.asp?presTarget=1644160<\/a><\/p>\n

          [5] https:\/\/www.regulations.gov\/document\/FDA-2020-N-1898-0246<\/a><\/p>\n

          [6] https:\/\/www.lifesitenews.com\/opinion\/cardiothoracic-surgeon-warns-fda-pfizer-on-immunological-danger-of-covid-vaccines-in-recently-convalescent-and-asymptomatic-carriers<\/a><\/p>\n

          [7]\u00a0https:\/\/media.tghn.org\/medialibrary\/2020\/11\/C4591001_Clinical_Protocol_Nov2020_Pfizer_BioNTech.pdf<\/a><\/p>\n

          [8]https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC6829615\/<\/a><\/p>\n

          [9] https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC6289228\/<\/a><\/p>\n

          [10] https:\/\/www.nejm.org\/doi\/full\/10.1056\/NEJMra2035343<\/a><\/p>\n

          [11] https:\/\/www.ahajournals.org\/doi\/10.1161\/CIRCRESAHA.121.318902<\/a><\/p>\n

          [12] https:\/\/www.goldegg-verlag.com\/goldegg-verlag\/wp-content\/uploads\/corona_unmasked_engl_leseprobe.pdf<\/a><\/p>\n

          Video interview: https:\/\/beforeitsnews.com\/u-s-politics\/2021\/04\/german-microbiologist-to-reduce-the-worlds-populationthey-are-killing-people-with-these-covid-vaccines-video-2582255.html<\/a><\/p>\n

          [13] https:\/\/journals.plos.org\/plosone\/article?id=10.1371%2Fjournal.pone.0035421<\/a><\/p>\n

          [14] https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC3209347\/<\/a><\/p>\n

          [15] https:\/\/www.bulatlat.com\/2020\/08\/21\/hazards-of-the-covid-19-vaccine\/<\/a><\/p>\n

          [16] https:\/\/virological.org\/t\/response-to-ncov2019-against-backdrop-of-endogenous-retroviruses\/396<\/a><\/p>\n

          [17] https:\/\/2020news.de\/wp-content\/uploads\/2020\/12\/Wodarg_Yeadon_EMA_Petition_Pfizer_Trial_FINAL_01DEC2020_EN_unsigned_with_Exhibits.pdf<\/a><\/p>\n

          [18] https:\/\/jermwarfare.com\/blog\/judy-mikovits-viruses<\/a><\/p>\n

          [19]\u00a0https:\/\/www.nature.com\/articles\/nature02145<\/p>\n

          [20] https:\/\/www.pnas.org\/content\/pnas\/118\/21\/e2105968118.full.pdf<\/a><\/p>\n

          [21] https:\/\/21a86421-c3e0-461b-83c2-cfe4628dfadc.filesusr.com\/ugd\/659775_265cb97bf3bc4d25927f8c074ca6b51d.pdf<\/a><\/p>\n

          ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~<\/p>\n

          Maggie Zhou\u00a0<\/strong>received\u00a0her PhD from the University of Wisconsin – Madison in 1997, and\u00a0worked as a computational biologist for a number of years.\u00a0 She is currently an independent seeker of truth.<\/em><\/p>\n

          ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~<\/p>\n

          ___
          \n          https:\/\/cyprusindymedia.blogspot.com\/2021\/05\/mechanisms-of-covid-vaccine-induced.html<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"

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