Department of Neurology and Neuroscience Center, The First Hospital of Jilin University, Xinmin Street 71#, Changchun, 130021, China.
Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Mol Neurobiol. 2021 Dec;58(12):6249-6271. doi: 10.1007/s12035-021-02495-7. Epub 2021 Sep 3.
Multiple sclerosis (MS) is an autoimmunity-related chronic demyelination disease of the central nervous system (CNS), causing young disability. Currently, highly specific immunotherapies for MS are still lacking. Programmed cell death 1 (PD-1) is an immunosuppressive co-stimulatory molecule, which is expressed on activated T lymphocytes, B lymphocytes, natural killer cells, and other immune cells. PD-L1, the ligand of PD-1, is expressed on T lymphocytes, B lymphocytes, dendritic cells, and macrophages. PD-1/PD-L1 delivers negative regulatory signals to immune cells, maintaining immune tolerance and inhibiting autoimmunity. This review comprehensively summarizes current insights into the role of PD-1/PD-L1 signaling in MS and its animal model experimental autoimmune encephalomyelitis (EAE). The potentiality of PD-1/PD-L1 as biomarkers or therapeutic targets for MS will also be discussed.
多发性硬化症(MS)是一种与自身免疫有关的中枢神经系统(CNS)慢性脱髓鞘疾病,导致年轻人残疾。目前,针对 MS 的高度特异性免疫疗法仍然缺乏。程序性细胞死亡蛋白 1(PD-1)是一种免疫抑制性共刺激分子,在活化的 T 淋巴细胞、B 淋巴细胞、自然杀伤细胞和其他免疫细胞上表达。PD-1 的配体 PD-L1 在 T 淋巴细胞、B 淋巴细胞、树突状细胞和巨噬细胞上表达。PD-1/PD-L1 向免疫细胞传递负调节信号,维持免疫耐受并抑制自身免疫。这篇综述全面总结了 PD-1/PD-L1 信号在多发性硬化症及其动物模型实验性自身免疫性脑脊髓炎(EAE)中的作用的最新认识。还将讨论 PD-1/PD-L1 作为多发性硬化症生物标志物或治疗靶点的潜力。