自身免疫
免疫系统
癌症免疫疗法
提吉特
免疫疗法
受体
封锁
免疫学
医学
信号转导
T细胞
癌症研究
生物
效应器
抗体
自身免疫性疾病
细胞
抑制性突触后电位
癌症
机制(生物学)
免疫
单克隆抗体
共刺激
炎症
移植排斥反应
神经科学
免疫检查点
免疫受体
免疫调节
免疫耐受
电池类型
竞争行为
作者
Kieran R. Adam,Aamir Suhail,Vijay K. Kuchroo,Dario A.A. Vignali
摘要
Inhibitory receptors (IRs) such as CTLA-4, PD-1, LAG3, TIM-3, and TIGIT are critical regulators of immune homeostasis, functioning to restrain excessive immune activation and prevent autoimmunity. While the blockade of IRs has transformed cancer immunotherapy by reinvigorating antitumor T cell responses, emerging strategies aim to harness the immunosuppressive potential of these receptors for treating autoimmune and inflammatory diseases. Agonistic antibodies that activate IR signaling have demonstrated promising results in preclinical models by promoting immune tolerance and suppressing pathological effector T cell functions. This review highlights recent progress in the development of agonistic IR-targeted therapies, examining their mechanisms of action, therapeutic efficacy, and the translational challenges that must be addressed to bring these innovative approaches into clinical practice for the management of autoimmunity and inflammatory disorders.
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