生物
自身免疫
免疫系统
免疫学
免疫耐受
免疫疗法
免疫
CD28
T细胞
作者
Kelly P. Burke,Apoorvi Chaudhri,Gordon J. Freeman,Arlene H. Sharpe
出处
期刊:Immunity
[Elsevier]
日期:2024-02-01
卷期号:57 (2): 223-244
被引量:8
标识
DOI:10.1016/j.immuni.2024.01.013
摘要
Immune responses must be tightly regulated to ensure both optimal protective immunity and tolerance. Costimulatory pathways within the B7:CD28 family provide essential signals for optimal T cell activation and clonal expansion. They provide crucial inhibitory signals that maintain immune homeostasis, control resolution of inflammation, regulate host defense, and promote tolerance to prevent autoimmunity. Tumors and chronic pathogens can exploit these pathways to evade eradication by the immune system. Advances in understanding B7:CD28 pathways have ushered in a new era of immunotherapy with effective drugs to treat cancer, autoimmune diseases, infectious diseases, and transplant rejection. Here, we discuss current understanding of the mechanisms underlying the coinhibitory functions of CTLA-4, PD-1, PD-L1:B7-1 and PD-L2:RGMb interactions and less studied B7 family members, including HHLA2, VISTA, BTNL2, and BTN3A1, as well as their overlapping and unique roles in regulating immune responses, and the therapeutic potential of these insights.
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