Okazaki Taku, Wang Jian
Graduate School of Medicine, Kyoto University, Department of Medical Chemistry, Sakyo-ku, Kyoto 606-8501, Japan.
Autoimmunity. 2005 Aug;38(5):353-7. doi: 10.1080/08916930500124072.
Programmed cell death 1 (PD-1) was isolated in 1992 by subtractive-hybridization technique, as a molecule whose expression is enhanced by apoptotic stimuli. Since then we have been analyzing the function of PD-1 in the regulation of immune responses. Generation of PD-1 deficient mice, pathophysiological analyses of autoimmune diseases in PD-1 deficient mice, identification of two ligands, and analyses of downstream events of PD-1 revealed that PD-1 prevents autoimmunity by inhibiting activation of self-reactive lymphocytes. These findings were further applied on human autoimmune diseases and single nucleotide polymorphisms (SNPs) on human PD-1 gene have been reported to link with systemic lupus erythematosus (SLE), rheumatoid arthritis (RA) and type I diabetes.
程序性细胞死亡蛋白1(PD-1)于1992年通过消减杂交技术分离得到,是一种其表达受凋亡刺激增强的分子。从那时起,我们一直在分析PD-1在免疫反应调节中的功能。通过生成PD-1缺陷小鼠、对PD-1缺陷小鼠自身免疫性疾病进行病理生理学分析、鉴定两种配体以及分析PD-1的下游事件,发现PD-1通过抑制自身反应性淋巴细胞的激活来预防自身免疫。这些发现进一步应用于人类自身免疫性疾病,并且据报道人类PD-1基因上的单核苷酸多态性(SNP)与系统性红斑狼疮(SLE)、类风湿性关节炎(RA)和I型糖尿病有关。