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毒理学病理学论坛:mRNA 疫苗安全性——甄别事实与虚构。

Toxicologic Pathology Forum: mRNA Vaccine Safety-Separating Fact From Fiction.

机构信息

The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.

GlaxoSmithKline, Waltham, Massachusetts, USA.

出版信息

Toxicol Pathol. 2024 Aug;52(6):333-342. doi: 10.1177/01926233241278298. Epub 2024 Sep 10.

Abstract

SARS-CoV-2 spread rapidly across the globe, contributing to the death of millions of individuals from 2019 to 2023, and has continued to be a major cause of morbidity and mortality after the pandemic. At the start of the pandemic, no vaccines or anti-viral treatments were available to reduce the burden of disease associated with this virus, as it was a novel SARS coronavirus. Because of the tremendous need, the development of vaccines to protect against COVID-19 was critically important. The flexibility and ease of manufacture of nucleic acid-based vaccines, specifically mRNA-based products, allowed the accelerated development of COVID-19 vaccines. Although mRNA-based vaccines and therapeutics had been in clinical trials for over a decade, there were no licensed mRNA vaccines on the market at the start of the pandemic. The rapid development of mRNA-based COVID-19 vaccines reduced serious complications and death from the virus but also engendered significant public concerns, which continue now, years after emergency-use authorization and subsequent licensure of these vaccines. This article summarizes and addresses some of the safety concerns that continue to be expressed about these vaccines and their underlying technology.

摘要

SARS-CoV-2 在全球范围内迅速传播,导致 2019 年至 2023 年数百万人死亡,并且在大流行之后仍然是发病率和死亡率的主要原因。在大流行开始时,没有疫苗或抗病毒治疗方法可用于减轻与这种病毒相关的疾病负担,因为它是一种新型 SARS 冠状病毒。由于巨大的需求,开发针对 COVID-19 的疫苗至关重要。基于核酸的疫苗,特别是基于 mRNA 的产品的灵活性和易于制造,使得 COVID-19 疫苗的快速开发成为可能。尽管基于 mRNA 的疫苗和疗法已经在临床试验中进行了十多年,但在大流行开始时,市场上还没有许可的 mRNA 疫苗。基于 mRNA 的 COVID-19 疫苗的快速开发减少了因该病毒导致的严重并发症和死亡,但也引起了公众的重大关注,这些关注在这些疫苗获得紧急使用授权和随后获得许可后的多年里仍在继续。本文总结并解决了一些关于这些疫苗及其基础技术的持续存在的安全问题。

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