T cell control of SARS-CoV-2: When, which, and where?

被引:6
作者
Diniz, Mariana O. [1 ]
Maini, Mala K. [1 ]
Swadling, Leo [1 ]
机构
[1] UCL, Inst Immun & Transplantat, Div Infect & Immun, Pears Bldg, London WC1E 6BT, England
基金
英国惠康基金;
关键词
SARS-CoV-2-specific T cells; Abortive infection; Tissue-resident; Mucosal vaccination; PROTECTION; VIRUS; INFLUENZA; RESPONSES; IMMUNITY; INFECTION; COVID-19; VACCINATION; ACTIVATION; CHALLENGE;
D O I
10.1016/j.smim.2023.101828
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Efficient immune protection against viruses such as SARS-CoV-2 requires the coordinated activity of innate immunity, B and T cells. Accumulating data point to a critical role for T cells not only in the clearance of established infection, but also for aborting viral replication independently of humoral immunity. Here we review the evidence supporting the contribution of antiviral T cells and consider which of their qualitative features favour efficient control of infection. We highlight how studies of SARS-CoV-2 and other coronaviridae in animals and humans have provided important lessons on the optimal timing (When), functionality and specificity (Which), and location (Where) of antiviral T cells. We discuss the clinical implications, particularly for the development of next-generation vaccines, and emphasise areas requiring further study.
引用
收藏
页数:17
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