Iwakura Yoichiro
Center for Experimental Medicine, Institute of Medical Science, University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo 108-8639, Japan.
Cytokine Growth Factor Rev. 2002 Aug-Oct;13(4-5):341-55. doi: 10.1016/s1359-6101(02)00021-7.
Expression of inflammatory cytokines is augmented in the joints of patients with rheumatoid arthritis (RA). We found that cytokine levels are also elevated in the joints of a mouse arthritis model, human T-cell leukemia virus type I (HTLV-I) transgenic (Tg) mouse. Depletion of IL-1 by gene targeting greatly reduced the incidence of the disease, indicating the importance of this cytokine in the development of arthritis. Furthermore, IL-1 receptor antagonist (IL-1Ra)-deficient mice develop autoimmunity and arthritis spontaneously. These observations suggest that excess IL-1 signaling the causes autoimmunity. We show that IL-1 activates the immune system non-specifically by inducing CD40L and OX40 co-signaling molecules on T cells. In this review, the roles of IL-1 in the development of autoimmunity and arthritis in mouse models will be discussed.
类风湿性关节炎(RA)患者关节中炎症细胞因子的表达会增加。我们发现,在小鼠关节炎模型——人I型T细胞白血病病毒(HTLV-I)转基因(Tg)小鼠的关节中,细胞因子水平也会升高。通过基因靶向去除白细胞介素-1(IL-1)可大大降低疾病的发病率,这表明该细胞因子在关节炎发展过程中具有重要作用。此外,缺乏白细胞介素-1受体拮抗剂(IL-1Ra)的小鼠会自发出现自身免疫和关节炎。这些观察结果表明,过量的IL-1信号传导会导致自身免疫。我们发现,IL-1通过诱导T细胞上的CD40L和OX40共信号分子,非特异性地激活免疫系统。在这篇综述中,我们将讨论IL-1在小鼠模型自身免疫和关节炎发展过程中的作用。