Department of Medicine, Columbia University, New York, NY 10032, USA.
Immunol Rev. 2010 Jan;233(1):79-96. doi: 10.1111/j.0105-2896.2009.00864.x.
Accumulating evidence from murine and human studies supports a key role for interleukin-17 (IL-17) and IL-21 in the pathogenesis of inflammatory arthritis. The pathways and molecular mechanisms that underlie the production of IL-17 and IL-21 are being rapidly elucidated. This review focuses on interferon regulatory factor 4 (IRF4), a member of the IRF family of transcription factors, which has emerged as a crucial controller of both IL-17 and IL-21 production. We first outline the complex role of IRF4 in the function of CD4(+) T cells and then discuss recent studies from our laboratory that have revealed a surprising role for components of Rho GTPase-mediated pathways in controlling the activity of IRF4. A better understanding of these novel pathways will hopefully provide new insights into mechanisms responsible for the development of inflammatory arthritis and potentially guide the design of novel therapeutic approaches.
越来越多的来自于啮齿动物和人类的研究证据支持白细胞介素-17(IL-17)和白细胞介素-21(IL-21)在炎症性关节炎发病机制中的关键作用。目前正在快速阐明产生 IL-17 和 IL-21 的途径和分子机制。这篇综述重点关注干扰素调节因子 4(IRF4),它是转录因子 IRF 家族的成员,已成为 IL-17 和 IL-21 产生的关键调控因子。我们首先概述了 IRF4 在 CD4(+)T 细胞功能中的复杂作用,然后讨论了我们实验室的最新研究结果,这些结果揭示了 Rho GTPase 介导途径的成分在控制 IRF4 活性方面的惊人作用。更好地了解这些新途径有望为炎症性关节炎发展的机制提供新的见解,并可能指导新型治疗方法的设计。