Andersson Anna K, Li Ching, Brennan Fionula M
Kennedy Institute of Rheumatology, Imperial College Faculty of Medicine, 1 Aspenlea Road, London W6 8LH, UK.
Arthritis Res Ther. 2008;10(2):204. doi: 10.1186/ar2370. Epub 2008 Mar 14.
Progress into the understanding of immunopathology in rheumatoid arthritis is reviewed in the present article with regard to pro-inflammatory cytokine production, cell activation and recruitment, and osteoclastogenesis. Studies highlight the potential importance of T helper 17 cells and regulatory T cells in driving and suppressing inflammation in rheumatoid arthritis, respectively, and highlight other potential T-cell therapeutic targets. The genetic associations of the HLA shared epitope alleles with antibodies to citrullinated peptides in rheumatoid arthritis patients indicate that T cells are providing help to B cells to produce autoantibodies, and there is increasing evidence that these autoantibodies are pathogenic in rheumatoid arthritis.
本文就促炎细胞因子产生、细胞活化与募集以及破骨细胞生成方面,对类风湿关节炎免疫病理学的认识进展进行了综述。研究强调了辅助性T细胞17和调节性T细胞在类风湿关节炎中分别驱动和抑制炎症的潜在重要性,并突出了其他潜在的T细胞治疗靶点。类风湿关节炎患者中HLA共享表位等位基因与瓜氨酸化肽抗体的遗传关联表明,T细胞正在辅助B细胞产生自身抗体,并且越来越多的证据表明这些自身抗体在类风湿关节炎中具有致病性。