GONG Hang, ZHAO Xin, CHEN Wen-xia, XUE Ni-na. Research progress of LAG-3 in tumor immunity and targeted drug developmentJ. Acta Pharmaceutica Sinica, 2025, 60(5): 1315-1324. DOI: 10.16438/j.0513-4870.2024-1290
Citation: GONG Hang, ZHAO Xin, CHEN Wen-xia, XUE Ni-na. Research progress of LAG-3 in tumor immunity and targeted drug developmentJ. Acta Pharmaceutica Sinica, 2025, 60(5): 1315-1324. DOI: 10.16438/j.0513-4870.2024-1290

Research progress of LAG-3 in tumor immunity and targeted drug development

  • Lymphocyte activation gene 3 (LAG-3) is an important inhibitory receptor on T cells, which plays a crucial role in tumor immune evasion. LAG-3 is primarily expressed on activated T cells, natural killer (NK) cells and B cells, et al. By binding to its ligands, LAG-3 inhibits T cell proliferation, activation, and effector functions. LAG-3 has emerged as the third immune checkpoint protein (ICP) used in clinical practice, following programmed death 1 (PD-1)/programmed death ligand 1 (PD-L1) and cytotoxic T lymphocyte-associated antigen 4 (CTLA-4). Currently, there has been at least 20 LAG-3-targeted drugs undergoing clinical trials. This article mainly reviews the structure, expression regulation, ligands, co-expressed ICP of LAG-3, as well as its application in tumor immunotherapy, and discusses the current challenges of targeting LAG-3 research.
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