T细胞对新冠病毒的反应

IF 26.9 1区 医学 Q1 IMMUNOLOGY
Alessandro Sette, John Sidney, Shane Crotty
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引用次数: 25

摘要

在过去两年半中产生的大量证据解决了T细胞在SARS-CoV-2感染和接种疫苗后的作用。感染或疫苗接种诱导具有多功能的多表位CD4和CD8 T细胞应答。早期T细胞反应与轻度COVID-19结局相关。与动物模型数据一致,这些结果表明抗体反应是预防感染的关键,T细胞反应也可能在降低疾病严重程度和控制感染方面发挥有价值的作用。接种疫苗后的T细胞记忆可维持至少6个月。虽然中和抗体反应受到SARS-CoV-2变异的影响,但大多数CD4和CD8 T细胞反应被保留。这篇综述强调了我们在了解T细胞对SARS-CoV-2和COVID-19疫苗的反应方面取得的广泛进展,以及仍然存在的数据和知识空白。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
T Cell Responses to SARS-CoV-2.

A large body of evidence generated in the last two and a half years addresses the roles of T cells in SARS-CoV-2 infection and following vaccination. Infection or vaccination induces multi-epitope CD4 and CD8 T cell responses with polyfunctionality. Early T cell responses have been associated with mild COVID-19 outcomes. In concert with animal model data, these results suggest that while antibody responses are key to prevent infection, T cell responses may also play valuable roles in reducing disease severity and controlling infection. T cell memory after vaccination is sustained for at least six months. While neutralizing antibody responses are impacted by SARS-CoV-2 variants, most CD4 and CD8 T cell responses are preserved. This review highlights the extensive progress made, and the data and knowledge gaps that remain, in our understanding of T cell responses to SARS-CoV-2 and COVID-19 vaccines.

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来源期刊
Annual review of immunology
Annual review of immunology 医学-免疫学
CiteScore
57.20
自引率
0.70%
发文量
29
期刊介绍: The Annual Review of Immunology, in publication since 1983, focuses on basic immune mechanisms and molecular basis of immune diseases in humans. Topics include innate and adaptive immunity; immune cell development and differentiation; immune control of pathogens (viruses, bacteria, parasites) and cancer; and human immunodeficiency and autoimmune diseases. The current volume of this journal has been converted from gated to open access through Annual Reviews' Subscribe to Open program, with all articles published under a CC BY license.
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