COVID VACCINES DANGEROUS BUT USELESS! Explosive Research by Harvard Medical Doctors: “SARS-Cov-2 Variants ESCAPE Immunity of mRNA Sera and become more Infectious”

COVID VACCINES DANGEROUS BUT USELESS! Explosive Research by Harvard Medical Doctors: “SARS-Cov-2 Variants ESCAPE Immunity of mRNA Sera and become more Infectious”

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by Fabio Giuseppe Carlo Carisio

VERSIONE IN ITALIANO

It is a disconcerting and explosive study which, if it were read carefully by government health authorities with no involvement with vaccine Big Pharma, would forever block the experiment on the human population conducted especially by advanced Western countries.

In a nutshell, it “certifies” that the variants of SARS-Cov-2 which multiply rapidly continue to elude the new boosters which are updated to the latest viral genotype but obviously do not have time to adapt to the current one.

Ergo mRNA gene serums, harmful for a myriad of adverse reactions ascertained by thousands of international studies published in the most famous medical journals, are not only dangerous but also practically USELESS!!!

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Explosive Harvard Doctor’s Study

The importance of the research entitled “Ongoing evolution of SARS-CoV-2 drives escape from mRNA vaccine-induced humoral immunity” derives from the fact which was conducted by various medical specialists from the renowned Ragon Institute of MGH (Massachusetts General Hospital), MIT, and Harvard.

The Ragon Institute of Mass General, MIT, and Harvard, – officially established in 2009, with a donation from the Phillip T. and Susan M. Ragon Foundation – brings together scientists and engineers from diverse fields to better understand the immune system and support human health. Our mission is to harness the immune system to prevent and cure human disease.

«Our mission is to harness the immune system to prevent and cure human disease» is its focus.

The lead physician and correspondent is Alejandro B. Balazs, principal investigator of the Ragon Institute, assistant professor at Harvard Medical School, and assistant investigator at Massachusetts General Hospital in Boston.

Together with him, the new paper was signed by specialists from the Vaccine and Immunotherapy Center, from the Pediatric Infectious Disease and from the Department of Pathology of the same hospital, from the Division of Geriatrics and Palliative Medicine, Alpert Medical School of Brown University, Providence, Rhode Island, from the Geriatric Research Education and Clinical Center, Louis Stokes Cleveland Department of Veterans Affairs Medical Center, Cleveland, Ohio.

Not only. Precisely to conduct this very delicate research Balazs was funded by the NIAID (the National Institute of Allergy and Infectious Diseases directed by the infamous Anthony Fauci until December 2022) and by the Massachusetts Consortium on Pathogenesis Preparedness (MassCPR) as can be read in the statement on any conflicts of interest.

UPDATE – Fauci’s Testimony before US Congress: “Pandemic from Lab Leak is not a Conspiracy Theory”.

SARS-Cov-2 Variants Escape mRNA Gene Serums as predicted by Montagnier

This is why the study

, although published in Pre-Print on 7 March in the famous journal MedrXiv, partner of the BMJ (formerly British Medical Journal) and therefore not yet peer-reviewed, can be considered yet another very reliable litmus test on the risible effectiveness of vaccines which, however, is not questioned by researchers, convinced that they can hope for a new generation of genetic serums…

In extreme summary, the Research Summary confirms the onset of “vaccine-resistant” variants as predicted already in 2020 by the Italian biologist Franco Trinca and the French microbiologist and virologist Luc Montagnier (both disappeared in anomalous and mysterious circumstances), by the Geert Vanden Bossche vaccines and confirmed by some previous studies.

«Since the COVID-19 pandemic began in 2020, viral sequencing has documented 131 individual mutations in the viral spike protein across 48 named variants. To determine the ability of vaccine-mediated humoral immunity to keep pace with continued SARS-CoV-2 evolution, we assessed the neutralization potency of sera from 76 vaccine recipients collected after 2 to 6 immunizations against a comprehensive panel of mutations observed during the pandemic».

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The sentences on the partial failure of the past (and ongoing) vaccination campaign are unequivocal, which can be considered total if associated with the recent study – published in peer-review in the specialist journal Frontiers in Immunology – which highlighted a greater danger of contracting the Covid-19 disease in a serious and lethal form, precisely because of the immune system weakened by the boosters (as predicted again by Montagnier and then proven by other studies)

«Remarkably, while many individual mutations that emerged between 2020 and 2022 exhibit escape from sera following primary vaccination, few escape boosted sera. However, progressive loss of neutralization was observed across newer variants, irrespective of vaccine doses» we can read it further in the abstract of the study.

«Importantly, an updated XBB.1.5 booster significantly increased titers against newer variants but not JN.1. These findings demonstrate that seasonal boosters improve titers against contemporaneous strains, but novel variants continue to evade updated mRNA vaccines, demonstrating the need for novel approaches to adequately control SARS-CoV-2 transmission».

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In light of these tragic and lapidary conclusions, who will have the courage to warn those Italians who have already been vaccinated with the seventh dose, i.e. the fifth booster of the Pfizer-Biontech or Moderna mRNA gene serums which however are based on the XBB.1.5 variant?

It is clear that these people, in light of the American study, are risking their lives for almost nothing.

Confirmation of the Increased Virulence of the Variants

In fact, two sentences written by scientists in the very technical “final” DISCUSSION on the history of variants and vaccination updates take on a disturbing relevance (link among the sources below).

«In addition to escape from vaccine sera, we found that mutations also contribute significantly to the ability of pseudovirus to infect cells, suggesting that variant selection is optimizing both antibody escape and viral entry. We found that spikes from variants post BA.1 produced pseudoviruses that were up to 30-fold better at transducing target cells than wild-type, suggesting that WT SARS-CoV-2 spike was not optimally configured for ACE2-dependent viral entry».

Breaking Study! mRNA Vaccines Associated with Long COVID Syndrome. As Suggested by Gospa News many months ago!

With sophisticated biochemical terms, the doctors of the Ragon Institute and other hospitals are confirming the problem of vaccine-resistance of the variants launched by Vanden Bossche and – in our modest and inexpert opinion – also giving a vague explanation on the Covid-breakthrough phenomena and on the high lethality of Covid in vaccinated people precisely for the interaction that Spike creates in the human body: where – as is known from other research – it can persist for up to 2 years causing mild disorders from Spike-Demic or very serious disorders from Spikeopathy.

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But the alarming sentences of the research led by Alejandro B. Balazs (which perhaps will however be classified with the name of the first signatory Roederer) are not yet finished:

«This highlights the ongoing challenge presented by continued evolution of SARS-CoV-2, which has largely outpaced attempts to update vaccines. Our findings support the development of novel vaccine and prevention modalities capable of eliciting broad protection against future variants/outbreaks».

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In the final part of the Discussion, the researchers admit some limitations of the study. Among them we highlight the most worrying ones:

«The study is limited to the evaluation of serum neutralizing antibodies to the spike protein for our pseudovirus neutralization assay, and does not take into account neutralizing antibodies to other proteins including the N and M proteins».

This means that the role of the “Double Proline” inserted into the mRNA genetic sera to make them more effective is totally ignored although it is fundamental to understanding the persistence of the Toxic Spike as discovered by the Italian bioimmunologist Mauro Mantovani.

Research Ignores Dangerous T Cell Reactions to Vaccines

But there is also a further limitation of the study reported by the authors themselves: It concerns one of the crucial aspects of the adverse reactions caused by mRNA gene sera. A gap that seems almost artfully designed so as not to put the finger in a wound…

«Furthermore, we did not assess other antibody- mediated functions such as complement deposition, antibody-dependent cellular cytotoxicity, or antibody-dependent cellular phagocytosis, which may contribute to protection even in the absence of neutralizing antibodies. We also did not assess the role of vaccine-elicited cellular immune responses mediated by T cells and NK cells, which are likely to play a key role in disease prevention for vaccine recipients».

T cells are the protein molecules of the immune system that act as communication signals between the cells of the immune system and between them and different organs and tissues.

But, if they go haywire, they can also cause a so-called “cytokine storm” and trigger devastating autoimmune reactions, especially in the heart and brain.

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In particular, it has been ascertained by recent biochemical studies and scientific articles that their functioning can be compromised due to the diabolical manipulation of the Pseudouridine nucleoside (base of RNA) built in the laboratory and inserted into mRNA genetic sera to allow the vectors to deceive the dendritic cells responsible for identifying and trying to eliminate foreign agents…

“Bitter in the end”, there is another major limitation of the research of American scholars: they have not at all considered the laboratory origin of SARS-Cov-2 and furthermore of the Omicron variant that generated the resistant pseudovirus JN.1..

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Fabio Giuseppe Carlo Carisio
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MEDRXIV – Ongoing evolution of SARS-CoV-2 drives escape from mRNA vaccine-induced humoral immunity

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