Coinhibitory receptor PD-1H preferentially suppresses CD4+ T cell-mediated immunity

被引:212
|
作者
Flies, Dallas B.
Han, Xue
Higuchi, Tomoe
Zheng, Linghua
Sun, Jingwei
Ye, Jessica Jane
Chen, Lieping
机构
[1] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT USA
[2] Yale Univ, Sch Med, Yale Canc Ctr, New Haven, CT USA
来源
JOURNAL OF CLINICAL INVESTIGATION | 2014年 / 124卷 / 05期
关键词
SURFACE SIGNALING MOLECULES; CONCANAVALIN-A; LIVER-INJURY; CANCER; ANTIBODY; STIMULATION; RADIATION; SAFETY; MODELS;
D O I
10.1172/JCI74589
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
T cell activation is regulated by the interactions of surface receptors with stimulatory and inhibitory ligands. Programmed death-1 homolog (PD-1H, also called VISTA) is a member of the CD28 family of proteins and has been shown to act as a coinhibitory ligand. on APCs that suppress T cell responses. Here, we determined that PD-1H functions as a coinhibitory receptor for CD4(+) T cells. CD4+ T cells in mice lacking PD-1H exhibited a dramatically increased response to antigen stimulation. Furthermore, delivery of a PD-1H-specific agonist mAb directly inhibited CD4(+) T cell activation both in vitro and in vivo, validating a coinhibitory function of PD-1H. In a murine model of acute hepatitis, administration of a PD-1H agonist mAb suppressed CD4(+) T cell-mediated acute inflammation. PD-1H-deficient animals were highly resistant to tumor induction in a murine brain glioma model, and depletion of CD4(+) T cells, but not CD8(+) T cells, promoted tumor formation. Together, our findings suggest that PD-1H has potential as a target of immune modulation in the treatment of human inflammation and malignancies.
引用
收藏
页码:1966 / 1975
页数:10
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