Bioinformatic and Experimental Analysis of T Cell Immune Reactivity to SARS-CoV-2 and its Variants

被引:10
|
作者
Tarke, Alison [1 ,2 ,3 ]
Grifoni, Alba [1 ]
Sette, Alessandro [1 ,4 ]
机构
[1] Jolla Inst Immunol LJI, Ctr Infect Dis & Vaccine Res, La Jolla, CA 92037 USA
[2] Univ Genoa, Dept Internal Med, Genoa, Italy
[3] Univ Genoa, Dept Expt Med, Genoa, Italy
[4] Univ Calif San Diego, Dept Med, Div Infect Dis & Global Publ Hlth, San Diego, CA 92093 USA
来源
FRONTIERS IN BIOINFORMATICS | 2022年 / 2卷
基金
美国国家卫生研究院;
关键词
SARS-CoV-2; T cells; variants; epitopes; vaccination; ANTIBODY; INFECTION; RESPONSES;
D O I
10.3389/fbinf.2022.876380
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Definition of the T cells responses to SARS-CoV-2 and associated variants is critical to understanding the complexity of adaptive immunity against SARS-CoV-2 infection. Several groups have investigated the T cells responses by both experimental and bioinformatical approaches. Here we summarize recent findings on CD4 and CD8 T cell responses to SARS-CoV-2 with particular emphasis on emerging variants of concern, consolidating the results on the impact of SARS-CoV-2 variants on T cell responses by performing an additional metanalysis emphasizing the lower impact of variant mutations in dominant T cell epitopes. The consensus is that the majority of T cell responses are conserved across all current SARS-CoV-2 variants, including Delta and Omicron. Thus, even in concomitance with reduced antibody and B cell responses, T cells can still provide a second line of antiviral immunity.
引用
收藏
页数:9
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