Lag-3, Tim-3, and TIGIT: Co-inhibitory Receptors with Specialized Functions in Immune Regulation

被引:1606
作者
Anderson, Ana C. [1 ,2 ,3 ]
Joller, Nicole [4 ]
Kuchroo, Vijay K. [1 ,2 ,3 ]
机构
[1] Brigham & Womens Hosp, Evergrande Ctr Immunol Dis, 75 Francis St, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Ann Romney Ctr Neurol Dis, 75 Francis St, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Boston, MA 02115 USA
[4] Univ Zurich, Inst Expt Immunol, CH-8057 Zurich, Switzerland
关键词
T-CELL IMMUNOGLOBULIN; INTERFERON-GAMMA PRODUCTION; CENTRAL-NERVOUS-SYSTEM; NATURAL-KILLER-CELLS; EXPRESSION DEFINES; EFFECTOR FUNCTION; CRYSTAL-STRUCTURE; MICE DEFICIENT; TH1; CELLS; ACTIVATION;
D O I
10.1016/j.immuni.2016.05.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Co-inhibitory receptors, such as CTLA-4 and PD-1, have an important role in regulating T cell responses and have proven to be effective targets in the setting of chronic diseases where constitutive co-inhibitory receptor expression on T cells dampens effector T cell responses. Unfortunately, many patients still fail to respond to therapies that target CTLA-4 and PD-1. The next wave of co-inhibitory receptor targets that are being explored in clinical trials include Lag-3, Tim-3, and TIGIT. These receptors, although they belong to the same class of receptors as PD-1 and CTLA-4, exhibit unique functions, especially at tissue sites where they regulate distinct aspects of immunity. Increased understanding of the specialized functions of these receptors will inform the rational application of therapies that target these receptors to the clinic.
引用
收藏
页码:989 / 1004
页数:16
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