Role of PD-1 in Regulating T-Cell Immunity

被引:252
作者
Jin, Hyun-Tak [2 ,3 ]
Ahmed, Rafi [2 ,3 ]
Okazaki, Taku [1 ,2 ,3 ]
机构
[1] Univ Tokushima, Inst Genome Res, Div Immune Regulat, Tokushima 7708503, Japan
[2] Emory Univ, Emory Vaccine Ctr, Sch Med, Atlanta, GA 30322 USA
[3] Emory Univ, Dept Microbiol & Immunol, Sch Med, Atlanta, GA 30322 USA
来源
NEGATIVE CO-RECEPTORS AND LIGANDS | 2011年 / 350卷
关键词
PROGRAMMED DEATH-1 PD-1; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; CHRONIC VIRAL-INFECTION; SYSTEMIC-LUPUS-ERYTHEMATOSUS; INDUCED UP-REGULATION; CLINICAL-SIGNIFICANCE; DEPENDENT MECHANISM; DENDRITIC CELLS; B7-H1; PD-L1; IFN-GAMMA;
D O I
10.1007/82_2010_116
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Programmed cell death-1 (PD-1) is a member of the CD28 superfamily that delivers negative signals upon interaction with its two ligands, PD-L1 or PD-L2. PD-1 and its ligands are broadly expressed and exert a wider range of immunoregulatory roles in T cells activation and tolerance compared with other CD28 family members. Subsequent studies show that PD-1-PD-L interaction regulates the induction and maintenance of peripheral tolerance and protect tissues from autoimmune attack. PD-1 and its ligands are also involved in attenuating infectious immunity and tumor immunity, and facilitating chronic infection and tumor progression. The biological significance of PD-1 and its ligand suggests the therapeutic potential of manipulation of PD-1 pathway against various human diseases. In this review, we summarize our current understanding of PD-1 and its ligands ranging from discovery to clinical significance.
引用
收藏
页码:17 / 37
页数:21
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