Overcoming T cell exhaustion in infection and cancer

被引:896
作者
Pauken, Kristen E.
Wherry, E. John [1 ]
机构
[1] Univ Penn, Perelman Sch Med, Inst Immunol, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
PD-1; PD-L1; T cell exhaustion; immunotherapy; cancer; chronic infection; INHIBITORY RECEPTOR PD-1; PROGRAMMED DEATH-1; VIRAL PERSISTENCE; UP-REGULATION; ANTI-PD-L1; ANTIBODY; CLINICAL ACTIVITY; TETRAMER BINDING; VIRUS-INFECTION; EPITOPE ESCAPE; CUTTING EDGE;
D O I
10.1016/j.it.2015.02.008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Inhibitors of the Programmed Cell Death 1: Programmed Cell Death 1 ligand 1 (PD-1:PD-L1) pathway, a central regulator of T cell exhaustion, have been recently shown to be effective for treatment of different cancers. However, clinical responses are mixed, highlighting the need to better understand the mechanisms of action of PD1:PD-L1, the role of this pathway in immunity to different tumors, and the molecular and cellular effects of PD-1 blockade. Here, we review the molecular regulation of T cell exhaustion, placing recent findings on PD-1 blockade therapies in cancer in the context of the broader understanding of the roles of the PD-1:PD-L1 pathway in T cell exhaustion during chronic infection. We discuss the current understanding of the mechanisms involved in reversing T cell exhaustion, and outline critical areas of focus for future research, both basic and clinical.
引用
收藏
页码:265 / 276
页数:12
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