提吉特
受体
生物
免疫受体
抑制性突触后电位
免疫系统
效应器
免疫学
细胞生物学
T细胞
神经科学
生物化学
作者
Ana C. Anderson,Nicole Joller,Vijay K. Kuchroo
出处
期刊:Immunity
[Elsevier]
日期:2016-05-01
卷期号:44 (5): 989-1004
被引量:1459
标识
DOI:10.1016/j.immuni.2016.05.001
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.
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