The Differentiation and Maintenance of SARS-CoV-2-Specific Follicular Helper T Cells

被引:5
|
作者
Wang, Yifei [1 ]
Tian, Qin [2 ,3 ]
Ye, Lilin [1 ,3 ]
机构
[1] Southern Med Univ, Sch Lab Med & Biotechnol, Guangdong Prov Key Lab Immune Regulat & Immunother, Guangzhou, Peoples R China
[2] Southern Med Univ, Dermatol Hosp, Guangzhou, Peoples R China
[3] Third Mil Med Univ, Inst Immunol, Peoples Liberat Army PLA, Chongqing, Peoples R China
基金
中国国家自然科学基金;
关键词
CD4(+) T cell; follicular helper T cell; Viral infection; COVID-19; SARS-CoV-2; CXC CHEMOKINE RECEPTOR-5; TRANSCRIPTION FACTOR; B-CELLS; ANTIBODY-RESPONSES; ANTIGEN PRESENTATION; NEGATIVE REGULATOR; GERMINAL-CENTERS; BCL-6; EXPRESSION; CD4(+); MEMORY;
D O I
10.3389/fcimb.2022.953022
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Upon acute viral infection, virus-specific CD4(+) T cells differentiate into either T(H)1 cells or follicular helper T (T-FH) cells. The molecular pathways governing such bimodal cell fate commitment remain elusive. Additionally, effector virus-specific T-FH cells further differentiate into corresponding memory population, which confer long-term protection against re-infection of same viruses by providing immediate help to virus-specific memory B cells. Currently, the molecular mechanisms underlying the long-term maintenance of memory T-FH cells are largely unknown. In this review, we discuss current understanding of early differentiation of virus-specific effector T-FH cells and long-term maintenance of virus-specific memory T-FH cells in mouse models of viral infection and patients of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection.
引用
收藏
页数:15
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