Ceeraz Sabrina, Nowak Elizabeth C, Burns Christopher M, Noelle Randolph J
Department of Microbiology and Immunology, Norris Cotton Cancer Center, Geisel School of Medicine at Dartmouth, 1 Medical Center Drive, Lebanon, NH 03756, USA.
Arthritis Res Ther. 2014;16(5):469. doi: 10.1186/s13075-014-0469-1.
Immune checkpoint regulators are critical modulators of the immune system, allowing the initiation of a productive immune response and preventing the onset of autoimmunity. Co-inhibitory and co-stimulatory immune checkpoint receptors are required for full T-cell activation and effector functions such as the production of cytokines. In autoimmune rheumatic diseases, impaired tolerance leads to the development of diseases such as rheumatoid arthritis, systemic lupus erythematosus, and Sjogren's syndrome. Targeting the pathways of the inhibitory immune checkpoint molecules CD152 (cytotoxic T lymphocyte antigen-4) and CD279 (programmed death-1) in cancer shows robust anti-tumor responses and tumor regression. This observation suggests that, in autoimmune diseases, the converse strategy of engaging these molecules may alleviate inflammation owing to the success of abatacept (CD152-Ig) in rheumatoid arthritis patients. We review the preclinical and clinical developments in targeting immune checkpoint regulators in rheumatic disease.
免疫检查点调节因子是免疫系统的关键调节因子,可启动有效的免疫反应并预防自身免疫的发生。共抑制性和共刺激性免疫检查点受体是T细胞完全激活和效应功能(如细胞因子产生)所必需的。在自身免疫性风湿性疾病中,耐受性受损会导致类风湿性关节炎、系统性红斑狼疮和干燥综合征等疾病的发展。在癌症中,靶向抑制性免疫检查点分子CD152(细胞毒性T淋巴细胞抗原4)和CD279(程序性死亡1)的途径显示出强大的抗肿瘤反应和肿瘤消退。这一观察结果表明,在自身免疫性疾病中,由于阿巴西普(CD152-Ig)在类风湿性关节炎患者中的成功应用,激活这些分子的相反策略可能会减轻炎症。我们综述了在风湿性疾病中靶向免疫检查点调节因子的临床前和临床进展。