Departments of Rheumatology and Immunology, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.
Semin Immunopathol. 2010 Mar;32(1):43-53. doi: 10.1007/s00281-009-0189-9. Epub 2010 Feb 4.
Th17 cells are implicated in human autoimmune diseases, such as rheumatoid arthritis (RA), although it has not been established whether this persistent destructive arthritis is driven by Th1 and/or Th17 cells. Interleukin-17A (IL-17A) contributes to the pathogenesis of arthritis as has been shown in several experimental arthritis models. Importantly, recent data from first clinical trials with anti-IL-17A antibody treatment in psoriatic arthritis patients and RA patients looks promising. This review summarizes the findings about the role of Th17 cells in arthritis and discusses the impact of the different Th17 cytokines in the pathogenesis of this disease. However, further studies are needed to unravel the interplay between IL-17A and other Th17 cytokines such as IL-17F, IL-22, and IL-21 in the pathoimmunological process of this crippling disease, in particular, whether regulating Th17 cell activity or specific combinations of Th17 cytokines will have additional value compared to neutralizing IL-17A activity alone. Moreover, tumor necrosis factor-positive Th17 cells are discussed as potential dangerous cells in driving persistent arthritis in human early RA.
Th17 细胞与人类自身免疫性疾病有关,如类风湿关节炎(RA),尽管尚未确定这种持续的破坏性关节炎是否由 Th1 和/或 Th17 细胞驱动。白介素-17A(IL-17A)在几种实验性关节炎模型中都有助于关节炎的发病机制。重要的是,最近在银屑病关节炎患者和 RA 患者的首次抗 IL-17A 抗体治疗临床试验中获得的数据显示出了希望。这篇综述总结了 Th17 细胞在关节炎中的作用的研究结果,并讨论了不同的 Th17 细胞因子在该疾病发病机制中的作用。然而,需要进一步的研究来阐明 IL-17A 和其他 Th17 细胞因子(如 IL-17F、IL-22 和 IL-21)在这种致残性疾病的病理免疫学过程中的相互作用,特别是调节 Th17 细胞活性或 Th17 细胞因子的特定组合是否会比单独中和 IL-17A 活性具有额外的价值。此外,还讨论了 TNF 阳性 Th17 细胞作为驱动人类早期 RA 持续关节炎的潜在危险细胞。