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由 1 代 COVID-19 疫苗诱导的异源免疫及其在开发泛冠状病毒疫苗中的作用。

Heterologous immunity induced by 1 generation COVID-19 vaccines and its role in developing a pan-coronavirus vaccine.

机构信息

Department of Surgery, Faculty of Medicine and Dentistry, College of Health Sciences, University of Alberta, Edmonton, AB, Canada.

出版信息

Front Immunol. 2022 Aug 15;13:952229. doi: 10.3389/fimmu.2022.952229. eCollection 2022.

DOI:10.3389/fimmu.2022.952229
PMID:36045689
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9420909/
Abstract

Severe acute respiratory syndrome virus-2 (SARS-CoV-2), the causative infectious agent of the COVID-19 pandemic, has led to multiple (4-6) waves of infections worldwide during the past two years. The development of vaccines against SARS-CoV-2 has led to successful mass immunizations worldwide, mitigating the worldwide mortality due the pandemic to a great extent. Yet the evolution of new variants highlights a need to develop a universal vaccine which can prevent infections from all virulent SARS-CoV-2. Most of the current first generation COVID-19 vaccines are based on the Spike protein from the original Wuhan-hu-1 virus strain. It is encouraging that they still protect from serious illnesses, hospitalizations and mortality against a number of mutated viral strains, to varying degrees. Understanding the mechanisms by which these vaccines provide heterologous protection against multiple highly mutated variants can reveal strategies to develop a universal vaccine. In addition, many unexposed individuals have been found to harbor T cells that are cross-reactive against SARS-CoV-2 antigens, with a possible protective role. In this review, we will discuss various aspects of natural or vaccine-induced heterologous (cross-reactive) adaptive immunity against SARS-CoV-2 and other coronaviruses, and their role in achieving the concept of a pan-coronavirus vaccine.

摘要

严重急性呼吸综合征冠状病毒 2 型(SARS-CoV-2)是导致 COVID-19 大流行的病原体,在过去两年中,已在全球引发了多波(4-6)波感染。针对 SARS-CoV-2 的疫苗的开发已在全球范围内实现了成功的大规模免疫接种,在很大程度上减轻了大流行造成的全球死亡率。然而,新变体的出现凸显出需要开发一种通用疫苗,以预防所有强毒 SARS-CoV-2 的感染。目前大多数第一代 COVID-19 疫苗都是基于原始武汉株的刺突蛋白。令人鼓舞的是,它们仍然可以在不同程度上预防多种突变病毒株引起的严重疾病、住院和死亡。了解这些疫苗如何针对多种高度突变的变体提供异源保护的机制,可以揭示开发通用疫苗的策略。此外,许多未暴露的个体被发现拥有针对 SARS-CoV-2 抗原的交叉反应性 T 细胞,可能具有保护作用。在这篇综述中,我们将讨论针对 SARS-CoV-2 和其他冠状病毒的天然或疫苗诱导的异源(交叉反应性)适应性免疫的各个方面,以及它们在实现泛冠状病毒疫苗概念方面的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52d/9420909/2c5b07651dbb/fimmu-13-952229-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52d/9420909/92566bd799df/fimmu-13-952229-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52d/9420909/afc04480498d/fimmu-13-952229-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52d/9420909/2c5b07651dbb/fimmu-13-952229-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52d/9420909/92566bd799df/fimmu-13-952229-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52d/9420909/afc04480498d/fimmu-13-952229-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52d/9420909/2c5b07651dbb/fimmu-13-952229-g003.jpg

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