Possible Unintended Consequences of the mRNA Vaccines Against COVID-19 針對 COVID-19 的 mRNA 疫苗的後果

Stephanie Seneff, a veteran scientist at MIT and Greg Nigh, a naturopathic oncologist have recently published a peer-reviewed article to raise some safety concern over mRNA vaccines manufactured by Moderna and Pfizer.

Here is the abstract

Operation Warp Speed brought to market in the United States two mRNA vaccines, produced by Pfizer and Moderna. Interim data suggested high efficacy for both of these vaccines, which helped legitimize Emergency Use Authorization (EUA) by the FDA. However, the exceptionally rapid movement of these vaccines through controlled trials and into mass deployment raises multiple safety concerns.

In this review we first describe the technology underlying these vaccines in detail. We then review both components of and the intended biological response to these vaccines, including production of the spike protein itself, and their potential relationship to a wide range of both acute and long-term induced pathologies, such as blood disorders, neurodegenerative diseases and autoimmune diseases. Among these potential induced pathologies, we discuss the relevance of prion-protein-related amino acid sequences within the spike protein.

We also present a brief review of studies supporting the potential for spike proteinshedding”, transmission of the protein from a vaccinated to an unvaccinated person, resulting in symptoms induced in the latter. 

We finish by addressing a common point of debate, namely, whether or not these vaccines could modify the DNA of those receiving the vaccination. While there are no studies demonstrating definitively that this is happening, we provide a plausible scenario, supported by previously established pathways for transformation and transport of genetic material, whereby injected mRNA could ultimately be incorporated into germ cell DNA for transgenerational transmission.

We conclude with our recommendations regarding surveillance that will help to clarify the long-term effects of these experimental drugs and allow us to better assess the true risk/benefit ratio of these novel technologies.

It seems that the authors are concerned mainly with two possible risks:

1) Spike protein may potentially cause Alzheimer’s disease or Parkinson disease.   Spike protein shedding may spread to the unvaccinated people and induce neurodegenerative diseases in them.  Dr. Seneff claims in an interview that the risk could manifest in 10 to 15 years in vaccinated people.

2) mRNA could potentially be integrated into a person’s DNA and permanently change the person’s genome.

麻省理工學院的資深科學家 Stephanie Seneff 和自然療法腫瘤學家 Greg Nigh 最近發表了一篇同行評議的文章,對 Moderna 和輝瑞公司生產的 mRNA 疫苗提出了一些安全問題。

這是摘要

Operation Warp Speed 將輝瑞和 Moderna 生產的兩種 mRNA 疫苗推向美國市場。中期數據表明,這兩種疫苗都具有很高的療效,這有助於使 FDA 的緊急使用授權 (EUA) 合法化。然而,這些疫苗通過對照試驗和大規模部署的異常迅速的轉移引發了多種安全問題。

在這篇綜述中,我們首先詳細描述了這些疫苗背後的技術。然後,我們回顧了這些疫苗的組成部分和預期的生物反應,包括刺突蛋白本身的產生,以及它們與各種急性和長期誘發的病理學的潛在關係,如血液疾病、神經退行性疾​​病和自身免疫性疾病。疾病。在這些潛在的誘發病理中,我們討論了刺突蛋白中朊病毒蛋白相關氨基酸序列的相關性。

我們還簡要回顧了支持刺突蛋白“脫落”可能性的研究,即蛋白質從接種疫苗的人傳播給未接種疫苗的人,導致後者誘發症狀。

我們最後解決了一個共同的爭論點,即這些疫苗是否可以改變接受疫苗接種者的 DNA。雖然沒有研究明確證明這種情況正在發生,但我們提供了一個合理的方案,由先前建立的遺傳物質轉化和運輸途徑支持,由此註射的 mRNA 最終可以整合到生殖細胞 DNA 中進行跨代傳遞。

最後,我們提出了有關監測的建議,這將有助於闡明這些實驗性藥物的長期影響,並使我們能夠更好地評估這些新技術的真實風險/收益比。

作者似乎主要關注兩種可能的風險:

1) 刺突蛋白可能會導致阿爾茨海默病或帕金森病。穗狀蛋白脫落可能會傳播到未接種疫苗的人群中並誘發他們的神經退行性疾​​病。 Seneff 博士在接受采訪時聲稱,接種疫苗的人可能會在 10 到 15 年內出現這種風險。

2) mRNA 有可能被整合到一個人的 DNA 中並永久地改變這個人的基因組。

$$$ 如果你愿意,你可以在这捐款支持我们。谢谢。$$$
$$$ If you would, you can make a donation here to support us. Thank you. $$$

16

No Responses

Write a response

five × two =