Revisiting the PD-1 pathway

被引:348
|
作者
Patsoukis, Nikolaos [1 ,2 ]
Wang, Qi [1 ,2 ]
Strauss, Laura [1 ,2 ,3 ]
Boussiotis, Vassiliki A. [1 ,2 ]
机构
[1] Harvard Med Sch, Beth Israel Deaconess Med Ctr, Div Hematol Oncol, Boston, MA 02215 USA
[2] Harvard Med Sch, Beth Israel Deaconess Med Ctr, Dept Med, Boston, MA 02215 USA
[3] EMD Serono Biller, EMD Serono R&D Inst, Immunopharmacol Immunooncol TIP, Billerica, MA 01821 USA
来源
SCIENCE ADVANCES | 2020年 / 6卷 / 38期
关键词
PROGRAMMED DEATH 1; T-CELL-ACTIVATION; TYROSINE-PHOSPHATASE; CRYSTAL-STRUCTURE; SOLUBLE PD-L1; NEGATIVE REGULATION; IMMUNE-RESPONSES; RECEPTOR; EXPRESSION; BLOCKADE;
D O I
10.1126/sciadv.abd2712
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Programmed Death-1 (PD-1; CD279) is an inhibitory receptor induced in activated T cells. PD-1 engagement by its ligands, PD-L1 and PD-L2, maintains peripheral tolerance but also compromises anti-tumor immunity. Blocking antibodies against PD-1 or its ligands have revolutionized cancer immunotherapy. However, only a fraction of patients develop durable antitumor responses. Clinical outcomes have reached a plateau without substantial advances by combinatorial approaches. Thus, great interest has recently emerged to investigate, in depth, the mechanisms by which the PD-1 pathway transmits inhibitory signals with the goal to identify molecular targets for improvement of the therapeutic success. These efforts have revealed unpredictable dimensions of the pathway and uncovered novel mechanisms involved in PD-1 and PD-L1 regulation and function. Here, we provide an overview of the recent advances on the mechanistic aspects of the PD-1 pathway and discuss the implications of these new discoveries and the gaps that remain to be filled.
引用
收藏
页数:13
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