B7 family checkpoint regulators in immune regulation and disease

被引:416
作者
Ceeraz, Sabrina [1 ]
Nowak, Elizabeth C. [1 ]
Noelle, Randolph J. [1 ,2 ]
机构
[1] Geisel Sch Med Dartmouth, Dept Microbiol & Immunol, Norris Cotton Canc Ctr, Lebanon, NH 03756 USA
[2] Kings Coll London, Guys Hosp, MRC, Ctr Transplantat, London SE1 9RT, England
基金
美国国家卫生研究院; 英国惠康基金;
关键词
T-CELL-ACTIVATION; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; MONOCLONAL-ANTIBODY TGN1412; DEATH-1; PD-1; PATHWAY; LUNG-CANCER CELL; PROGRAMMED DEATH-1; CD28; COSTIMULATION; PROSTATE-CANCER; GASTRIC-CANCER; NOD MICE;
D O I
10.1016/j.it.2013.07.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Fine-tuning the immune response and maintaining tolerance to self-antigens involves a complex network of co-stimulatory and co-inhibitory molecules. The recent FDA approval of ipilimumab, a monoclonal antibody blocking cytotoxic T lymphocyte antigen (CTLA)-4, demonstrates the impact of checkpoint regulators in disease. This is reinforced by ongoing clinical trials targeting not only CTLA-4, but also the programmed death (PD)-1 and B7-H4 pathways in various disease states. Recently, two new B7 family inhibitory ligands, V-domain Ig suppressor of T cell activation (VISTA) and B7-H6 were identified. Here, we review recent understanding of B7 family members and their concerted regulation of the immune response to either self or foreign pathogens. We also discuss clinical developments in targeting these pathways in different disease settings, and introduce VISTA as a putative therapeutic target.
引用
收藏
页码:556 / 563
页数:8
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