Oncoimmunology Group, Navarrabiomed-Public University of Navarre, IdISNA, 31008 Pamplona, Navarra, Spain.
Department of Medical Oncology, Complejo Hospitalario de Navarra CHN-IdISNA, 31008 Pamplona, Navarra, Spain.
Int J Mol Sci. 2021 May 17;22(10):5282. doi: 10.3390/ijms22105282.
Lymphocyte activation gene 3 (LAG-3) is a cell surface inhibitory receptor with multiple biological activities over T cell activation and effector functions. LAG-3 plays a regulatory role in immunity and emerged some time ago as an inhibitory immune checkpoint molecule comparable to PD-1 and CTLA-4 and a potential target for enhancing anti-cancer immune responses. LAG-3 is the third inhibitory receptor to be exploited in human anti-cancer immunotherapies, and it is considered a potential next-generation cancer immunotherapy target in human therapy, right next to PD-1 and CTLA-4. Unlike PD-1 and CTLA-4, the exact mechanisms of action of LAG-3 and its relationship with other immune checkpoint molecules remain poorly understood. This is partly caused by the presence of non-conventional signaling motifs in its intracellular domain that are different from other conventional immunoregulatory signaling motifs but with similar inhibitory activities. Here we summarize the current understanding of LAG-3 signaling and its role in LAG-3 functions, from its mechanisms of action to clinical applications.
淋巴细胞激活基因 3(LAG-3)是一种细胞表面抑制性受体,对 T 细胞激活和效应功能具有多种生物学活性。LAG-3 在免疫中发挥调节作用,不久前被认为是一种与 PD-1 和 CTLA-4 相当的抑制性免疫检查点分子,也是增强抗肿瘤免疫反应的潜在靶点。LAG-3 是在人类抗肿瘤免疫疗法中被利用的第三个抑制性受体,被认为是人类治疗中潜在的下一代癌症免疫治疗靶点,仅次于 PD-1 和 CTLA-4。与 PD-1 和 CTLA-4 不同,LAG-3 的作用机制及其与其他免疫检查点分子的关系尚不完全清楚。这部分是由于其细胞内结构域中存在非传统的信号基序,这些信号基序与其他常规免疫调节信号基序不同,但具有相似的抑制活性。本文总结了 LAG-3 信号及其在 LAG-3 功能中的作用的最新认识,包括其作用机制及其与其他免疫检查点分子的关系。