PD-L1
免疫疗法
癌症免疫疗法
癌症研究
蛋白酶体
癌症
程序性细胞死亡
蛋白质降解
肿瘤微环境
癌细胞
T细胞
免疫检查点
免疫抑制
免疫系统
嵌合抗原受体
细胞毒性T细胞
医学
化学
生物
抗原
黑色素瘤
免疫学
细胞生物学
细胞凋亡
生物化学
遗传学
作者
Qian Gou,Dong Chen,Huihui Xu,Bibimaryam Khan,Jianhua Jin,Qian Liu,Juanjuan Shi,Yongzhong Hou
标识
DOI:10.1038/s41419-020-03140-2
摘要
Abstract Programmed death ligand 1 (PD-L1, CD274) is an essential immune checkpoint protein that binds to programmed death 1 (PD-1) on T-lymphocytes. T cell plays a critical role in killing cancer cells while the cancer cell exhibits immune escape by the expression of PD-L1. The binding of PD-L1 to PD-1 inhibits T cell proliferation and activity, leading to tumor immunosuppression. Increasing evidence shows that PD-L1 protein undergoes degradation in proteasomes or lysosomes by multiple pathways, leading to enhanced immunotherapy for cancer. Although some specific drugs induce PD-L1 degradation and increase antitumor activity, the combination of these drugs with PD-L1/PD-1 blockade significantly enhances cancer immunotherapy. In this review, we have discussed the interaction of PD-L1 degradation with cancer immunotherapy.
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