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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.
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页数:9
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