T Cell Responses to SARS-CoV-2

被引:86
|
作者
Sette, Alessandro [1 ,2 ]
Sidney, John [1 ]
Crotty, Shane [1 ,2 ]
机构
[1] La Jolla Inst Immunol, Ctr Infect Dis & Vaccine Res, La Jolla, CA 92037 USA
[2] Univ Calif San Diego, Div Infect Dis & Global Publ Hlth, Dept Med, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
COVID-19; variants; infection; vaccination; disease severity; epitopes; IMMUNE-RESPONSES; ENDEMIC CORONAVIRUSES; COVID-19; VACCINATION; ANTIGEN-SPECIFICITY; ANTIBODY-RESPONSES; SARS CORONAVIRUS; CHADOX1; NCOV-19; INFECTION; MEMORY; PROTECTION;
D O I
10.1146/annurev-immunol-101721-061120
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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. Tcell 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.
引用
收藏
页码:343 / 373
页数:31
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