Division for Immune Receptors and T Cell Activation, Institute of Immunology, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
FASEB J. 2024 Nov 30;38(22):e70190. doi: 10.1096/fj.202401639R.
LAG-3 is a member of the immunoglobulin superfamily expressed on activated T cells, but also on other immune cells. It has significant homology to CD4. Both molecules have four extracellular Ig-like domains with similar structural motifs but the sequence identity between LAG-3 and CD4 is low. Furthermore, unlike CD4 LAG-3 restrains T cell responses and antibodies targeting this receptor are emerging drugs in cancer immunotherapy. A combination of LAG-3 and PD-1 antibodies has already been approved for the treatment of metastatic melanoma. Despite this success, its biology is still not well understood. Here we summarize the current knowledge on expression, ligands, and function of LAG-3. We point to the differences between LAG-3 and other inhibitory immune checkpoints and describe obstacles to study the role of this receptor in T cell activation processes. Finally, we discuss future directions for scientific efforts to come to a more complete understanding of the biology of this eminent immune checkpoint.
LAG-3 是免疫球蛋白超家族的成员,表达于活化的 T 细胞上,但也表达于其他免疫细胞上。它与 CD4 具有显著的同源性。这两个分子都有四个细胞外 Ig 样结构域,具有相似的结构基序,但 LAG-3 与 CD4 的序列同一性较低。此外,与 CD4 不同的是,LAG-3 抑制 T 细胞反应,针对该受体的抗体是癌症免疫治疗中的新兴药物。LAG-3 和 PD-1 抗体的联合已被批准用于治疗转移性黑色素瘤。尽管取得了这一成功,但它的生物学特性仍未得到很好的理解。在这里,我们总结了 LAG-3 的表达、配体和功能的最新知识。我们指出了 LAG-3 与其他抑制性免疫检查点之间的差异,并描述了研究该受体在 T 细胞激活过程中的作用所面临的障碍。最后,我们讨论了未来的科学努力方向,以更全面地了解这个重要的免疫检查点的生物学特性。