Joe B, Griffiths M M, Remmers E F, Wilder R L
Inflammatory Joint Diseases Section, Arthritis and Rheumatism Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institute of Health, Building 10, Room 9N240, 9000 Rockville Pike, Bethesda, MD 20892, USA.
Curr Rheumatol Rep. 1999 Dec;1(2):139-48. doi: 10.1007/s11926-999-0011-7.
The major, extensively studied, experimentally-induced rat and mouse models of arthritis with features resembling rheumatoid arthritis are reviewed here. Etiopathogenetic studies that were recently published are emphasized. In summary, multiple triggering stimuli can induce disease in genetically-prone strains of inbred rats and mice. Multiple genetic loci, including both MHC and non-MHC, regulate disease expression in these animals. By comparison with other models of autoimmune disease, clustering of regulatory loci within and among species is increasingly becoming evident. At the cellular level, both innate and acquired immune systems are involved in the disease manifestations. At the molecular level, unbalanced chronic production of tumor necrosis factor-alpha (TNF-alpha), interleukin (IL)-1, IL-6 and IL-12, as opposed to IL-4 and IL-10, is correlated with arthritis disease susceptibility and severity.
本文综述了主要的、经过广泛研究的、实验诱导的具有类风湿关节炎特征的大鼠和小鼠关节炎模型。重点介绍了最近发表的病因学研究。总之,多种触发刺激可在近交系大鼠和小鼠的遗传易感性品系中诱发疾病。多个基因位点,包括主要组织相容性复合体(MHC)和非MHC基因位点,调节这些动物的疾病表达。与其他自身免疫性疾病模型相比,物种内和物种间调节位点的聚集越来越明显。在细胞水平上,先天性和获得性免疫系统均参与疾病表现。在分子水平上,与白细胞介素(IL)-4和IL-10相反,肿瘤坏死因子-α(TNF-α)、IL-1、IL-6和IL-12的慢性不平衡产生与关节炎疾病易感性和严重程度相关。