一种新的克雅氏病的出现:注射COVID-19后几天26例人类疯牛病

Jean-claude Perez, C. Moret-Chalmin, L. Montagnier
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引用次数: 4

摘要

克雅氏病(Creutzfeldt-Jakob Disease)是一种以前罕见但普遍致命的人类朊病毒疾病,通常在几十年后才会导致死亡。在本文的附录中,我们强调了在原始SARS-CoV-2的刺突蛋白中以及在由武汉病毒构建的所有“疫苗”变体中存在朊病毒区域。SARS-CoV-2刺突中的朊病毒区域的突变密度是刺突其余部分的8倍,然而,奇怪的是,整个朊病毒区域在欧米克隆变体中完全消失了。在本文的主体部分,我们介绍了26例克雅氏病,所有病例均于2021年被诊断出来,在辉瑞、Moderna或阿斯利康注射COVID-19后平均11.38天内出现首次症状。由于这些非典型和新的人类朊病毒疾病病例的因果进展,发病机制-这些病例显然是一种全新形式的快速发展的克-雅各布病-我们关注症状发展的年表。我们从记忆的角度来考虑这一点——我们将克-雅各布病在covid前的典型发展与26例检查病例中类似症状的极端加速发展进行比较。通过这种方法,我们希望找出对理解这种新的和更快发展的人类朊病毒疾病至关重要的发病机制。通过回顾过去亚急性和缓慢发展的疾病的顺序途径,并将其与这种新的、极急性、快速发展的朊病毒疾病(在一次或多次注射COVID-19后紧随其后)进行比较,我们认为正确的推断是注射导致了这26例疾病。如果是这样的话,它们可能还导致了许多其他病例,由于它们的快速死亡而未被诊断出来。到2021年底,有20人在违规注射后的4.76个月内死亡。其中8人在2.5个月内突然死亡,证实了这种加速形式的克雅氏病的快速进展。到2022年6月,又有5名患者死亡,在撰写本文时,只有1名患者仍然活着。
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Emergence of a New Creutzfeldt-Jakob Disease: 26 Cases of the Human Version of Mad-Cow Disease, Days After a COVID-19 Injection
Creutzfeldt-Jakob Disease, the formerly rare but universally fatal prion disease in humans, normally progresses over several decades before it leads to death. In the Appendix to this paper, we highlight the presence of a prion region in the spike protein of the original SARS-CoV-2, and in all the “vaccine” variants built from the Wuhan virus. The prion region in the spike of SARS-CoV-2 has a density of mutations eight times greater than that of the rest of the spike, and, yet, strangely that entire prion region disappears completely in the Omicron variant. In the main body of our text, we present 26 cases of Creuzfeldt-Jacob Disease, all diagnosed in 2021 with the first symptoms appearing within an average of 11.38 days after a Pfizer, Moderna, or AstraZeneca COVID-19 injection. Because the causal progression, the etiopathogenesis, of these atypical and new cases of human prion disease — cases of what is apparently a totally new form of rapidly developing Creuzfeldt-Jacob Disease — we focus on the chronology of the symptomatic development. We consider it from an anamnestic point of view — one in which we compare the typical development of pre-COVID cases of Creuzfeldt-Jacob Disease to the extremely accelerated development of similar symptoms in the 26 cases under examination. By such an approach, we hope to work out the etiopathogenesis critical to understanding this new and much more rapidly developing human prion disease. By recalling the sequential pathway of that the formerly subacute and slowly developing disease followed in the past, and by comparing it with this new, extremely acute, rapidly developing prion disease — one following closely after one or more of the COVID-19 injections — we believe it is correct to infer that the injections caused the disease in these 26 cases. If so, they have probably also caused a many other cases that have gone undiagnosed because of their rapid progression to death. By late 2021, 20 had died within 4.76 months of the offending injection. Of those, 8 died suddenly within 2.5 months confirming the rapid progression of this accelerated form of Creuzfeldt-Jacob Disease. By June 2022, 5 more patients had died, and at the time of this current writing, only 1 remains still alive.
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