易普利姆玛
免疫学
免疫系统
抗原
CTLA-4号机组
细胞毒性T细胞
单克隆抗体
疾病
抑制器
T细胞
生物
免疫疗法
免疫检查点
医学
癌症研究
癌症
抗体
体外
遗传学
内科学
作者
Sabrina Ceeraz,Elizabeth C. Nowak,Randolph J. Noelle
标识
DOI:10.1016/j.it.2013.07.003
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.
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