At the Bedside: CTLA-4-and PD-1-blocking antibodies in cancer immunotherapy

被引:269
作者
Callahan, Margaret K. [1 ,2 ]
Wolchok, Jedd D. [1 ,2 ,3 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Melanoma & Sarcoma Serv, Dept Med, New York, NY 10065 USA
[2] Cornell Univ, Weill Med Coll, New York, NY 10021 USA
[3] Ludwig Inst Canc Res, New York, NY USA
关键词
tumor; overall survival; endpoints; T-CELL RESPONSES; ADVANCED MELANOMA PATIENTS; PHASE-II TRIAL; PROGRAMMED DEATH-1; ANTITUMOR IMMUNITY; IFN-GAMMA; AUTOIMMUNE HYPOPHYSITIS; REGULATORY T; B7-H1; PD-L1; COMBINATION IMMUNOTHERAPY;
D O I
10.1189/jlb.1212631
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
It is increasingly appreciated that cancers are recognized by the immune system, and under some circumstances, the immune system may control or even eliminate tumors. The modulation of signaling via coinhibitory or costimulatory receptors expressed on T cells has proven to be a potent way to amplify antitumor immune responses. This approach has been exploited successfully for the generation of a new class of anticancer therapies, checkpoint-blocking antibodies, exemplified by the recently FDA-approved agent, ipilimumab, an antibody that blocks the coinhibitory receptor CTLA-4. Capitalizing on the success of ipilimumab, agents that target a second coinhibitory receptor, PD-1, or its ligand, PD-L1, are in clinical development. Lessons learned from treating patients with CTLA-4 and PD-1 pathway-blocking antibodies will be reviewed, with a focus on concepts likely to inform the clinical development and application of agents in earlier stages of development. See related review At the bench: Preclinical rationale for CTLA-4 and PD-1 blockade as cancer immunotherapy.
引用
收藏
页码:41 / 53
页数:13
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