CD86
CTLA-4号机组
抗原提呈细胞
CD80
细胞毒性T细胞
细胞生物学
抗原
生物
免疫系统
T细胞
树突状细胞
化学
免疫学
CD40
体外
生物化学
作者
Murat Tekgüç,James B. Wing,Motonao Osaki,Jia Long,Shimon Sakaguchi
标识
DOI:10.1073/pnas.2023739118
摘要
DCs. Thus, Tregs are able to inhibit the T cell stimulatory activity of APCs by reducing their CD80/CD86 expression via CTLA-4-dependent trogocytosis. This CD80/CD86 reduction on APCs is able to exert dual suppressive effects on T cell immune responses by limiting CD80/CD86 costimulation to naïve T cells and by increasing free PD-L1 available for the inhibition of programmed death-1 (PD-1)-expressing effector T cells. Blockade of CTLA-4 and PD-1/PD-L1 in combination may therefore synergistically hinder Treg-mediated immune suppression, thereby effectively enhancing immune responses, including tumor immunity.
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