Department of Surgery and Cancer, Imperial College London, London, UK.
Department of Clinical and Experimental Medicine, University of Surrey, Faculty of Health and Medical Sciences, Guildford, Surrey, UK.
J Clin Pathol. 2021 Sep;74(9):543-547. doi: 10.1136/jclinpath-2021-207517. Epub 2021 Jun 28.
Lymphocyte-activation gene 3 (LAG-3) is a coreceptor found on activated T-lymphocytes activated B-lymphocytes and natural killer (NK) cells. It is closely related to CD4 where it shares multiple common and divergent features. It contains specific binding sites with high affinity to major histocompatibility complex (MHC) Class II and functions as an inhibitor of T-cell signalling. Tumour-infiltrating lymphocytes with high LAG-3 expression have been found in many solid tumours including ovarian cancer, melanoma, colorectal cancer and haematological malignancies including Hodgkin and diffuse large B-cell lymphoma. LAG-3 antagonism has been demonstrated to restore the anti-tumourigenic function of T-cells in vivo, however, mechanistic knowledge remains relatively poorly defined. As other immune checkpoint inhibitors have transformed the management of difficult to treat cancers, such as melanoma, it is hoped that LAG-3 might have the same potential. This review will explore LAG-3 modulation as an anticancer therapy, highlighting recent clinical developments.
淋巴细胞激活基因 3(LAG-3)是一种在活化的 T 淋巴细胞、B 淋巴细胞和自然杀伤(NK)细胞上发现的核心受体。它与 CD4 密切相关,在那里它共享多个共同和不同的特征。它包含与主要组织相容性复合体(MHC)II 类具有高亲和力的特异性结合位点,并作为 T 细胞信号转导的抑制剂。在许多实体瘤中,包括卵巢癌、黑色素瘤、结直肠癌和血液恶性肿瘤,包括霍奇金和弥漫性大 B 细胞淋巴瘤,已经发现了具有高 LAG-3 表达的肿瘤浸润淋巴细胞。已经证明 LAG-3 拮抗作用可以恢复体内 T 细胞的抗肿瘤功能,然而,其机制知识仍然相对缺乏。随着其他免疫检查点抑制剂改变了黑色素瘤等难以治疗癌症的治疗方法,人们希望 LAG-3 可能具有相同的潜力。本文将探讨 LAG-3 调节作为一种抗癌疗法,重点介绍最近的临床进展。