Anti-PD-1/PD-L1 therapy of human cancer: past, present, and future

被引:1518
作者
Chen, Lieping [1 ]
Han, Xue [1 ]
机构
[1] Yale Univ, Sch Med, Dept Immunobiol, Dermatol Med & Canc Immunol Program,Yale Canc Ctr, New Haven, CT 06511 USA
关键词
B7; FAMILY; T-CELLS; ADVANCED MELANOMA; CLINICAL ACTIVITY; DENDRITIC CELLS; PHASE-I; B7-H1; PD-1; BLOCKADE; CTLA-4;
D O I
10.1172/JCI80011
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Major progress has been made toward our understanding of the programmed death-1/programmed death ligand-1 (PD-1/PD-L1) pathway (referred to as the PO pathway). mAbs are already being used to block the PD pathway to treat human cancers (anti-PD therapy), especially advanced solid tumors. This therapy is based on principles that were discovered through basic research more than a decade ago, but the great potential of this pathway to treat a broad spectrum of advanced human cancers is just now becoming apparent. In this Review, we will briefly review the history and development of anti-PD therapy, from the original benchwork to the most up-to-date clinical results. We will then focus the discussion on three basic principles that define this unique therapeutic approach and highlight how anti-PD therapy is distinct from other immunotherapeutic approaches, namely tumor site immune modulation, targeting tumor-induced immune defects, and repairing ongoing (rather than generating de novo) tumor immunity. We believe that these fundamental principles set the standard for future immunotherapies and will guide our efforts to develop more efficacious and less toxic immune therapeutics to treat human cancers.
引用
收藏
页码:3384 / 3391
页数:8
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