LFA-1 in T cell priming, differentiation, and effector functions

被引:50
|
作者
Gerard, Audrey [1 ]
Cope, Andrew P. [2 ]
Kemper, Claudia [3 ,4 ]
Alon, Ronen [5 ]
Kochl, Robert [6 ]
机构
[1] Univ Oxford, Kennedy Inst Rheumatol, Oxford, England
[2] Kings Coll London, Ctr Inflammat Biol & Canc Immunol, London, England
[3] NHLBI, NIH, CIRS, Bldg 10, Bethesda, MD 20892 USA
[4] Univ Lubeck, Inst System Inflammat Res, Lubeck, Germany
[5] Weizmann Inst Sci, Rehovot, Israel
[6] Kings Coll London, Peter Gorer Dept Immunobiol, London, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金; 以色列科学基金会;
关键词
ANTIGEN-PRESENTING CELLS; COFACTOR PROTEIN CD46; DENDRITIC CELLS; LYMPH-NODES; IN-VIVO; IMMUNOLOGICAL SYNAPSE; ADHESION MOLECULE; IMMUNE-RESPONSE; ACTIVATION; COMPLEMENT;
D O I
10.1016/j.it.2021.06.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The integrin LFA-1 is crucial for T cell entry into mammalian lymph nodes and tissues, and for promoting interactions with antigen-presenting cells (APCs). However, it is increasingly evident that LFA-1 has additional key roles beyond the mere support of adhesion between T cells, the endothelium, and/or APCs. These include roles in homotypic T cell-T cell (T-T) communication, the induction of intracellular complement activity underlying Th1 effector cell polarization, and the support of long-lasting T cell memory. Here, we briefly summarize current knowledge of LFA-1 biology, discuss novel cytoskeletal regulators of LFA-1 functions, and review new aspects of LFA-1 mechanobiology that are relevant to its function in immunological synapses and in specific pathologies arising from LFA-1 dysregulation.
引用
收藏
页码:706 / 722
页数:17
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