Inhibitors of the PD-1 Pathway in Tumor Therapy

被引:116
作者
LaFleur, Martin W. [1 ,2 ]
Muroyama, Yuki [3 ,4 ]
Drake, Charles G. [4 ,5 ]
Sharpe, Arlene H. [1 ,6 ,7 ]
机构
[1] Harvard Med Sch, Dept Microbiol & Immunobiol, 77 Ave Louis Pasteur,NRB-837, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Dept Pediat Oncol, Boston, MA 02115 USA
[3] Johns Hopkins Univ, Sch Med, Dept Oncol, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21231 USA
[4] Columbia Univ, Med Ctr, Columbia Ctr Translat Immunol, New York, NY 10032 USA
[5] Columbia Univ, Med Ctr, Herbert Irving Comprehens Canc Ctr, New York, NY 10032 USA
[6] Harvard Med Sch, Evergrande Ctr Immunol Dis, Boston, MA 02115 USA
[7] Brigham & Womens Hosp, 75 Francis St, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
CD8(+) T-CELLS; LONG-TERM SAFETY; METASTATIC UROTHELIAL CARCINOMA; OPEN-LABEL; PROGRAMMED DEATH-1; ADVANCED MELANOMA; LUNG-CANCER; SINGLE-ARM; ACQUIRED-RESISTANCE; ANTITUMOR IMMUNITY;
D O I
10.4049/jimmunol.1701044
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The programmed death 1 (PD-1) pathway delivers inhibitory signals that function as a brake for immune responses. This pathway limits the initiation and duration of immune responses, thereby protecting tissues from immune-mediated damage and autoimmune diseases. However, the PD-1 pathway also inhibits immune responses to tumors. The critical role of PD-1 in preventing antitumor immunity is demonstrated by the transformative effects of PD-1 pathway blockade in a broad range of cancers with the hallmark of durability of response. Despite this success, most patients do not respond to PD-1 monotherapy, and some patients experience adverse events. In this review, we discuss the functions of the PD-1 pathway and its translation to cancer immunotherapy. We also consider current challenges and opportunities for PD-1 cancer immunotherapy, including mechanisms of response and resistance, identification of biomarkers of response to PD-1 therapy, characterization and treatment of PD-1 therapy-related adverse events, and development of safe and effective combination therapies.
引用
收藏
页码:375 / 383
页数:9
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