Institute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, Scotland, UK.
Immunol Cell Biol. 2012 Mar;90(3):288-92. doi: 10.1038/icb.2011.114. Epub 2012 Jan 17.
Elucidating pathways that regulate cytokine production in the context of autoimmune disease will likely lead to the development of novel therapeutics. Herein, we review data suggesting that microRNAs (miRs) represent one such level of regulatory activity, with particular emphasis on the pathogenesis of rheumatoid arthritis (RA). A series of miRs have been identified to be dysregulated in cell subsets within the articular compartment of patients with RA. These have a critical role in regulating cartilage-invading phenotype of RA synovial fibroblasts. More recently, several studies suggest that miRs also regulate leukocyte activation and cytokine production that in turn contribute to the immunologic component of effector synovial pathology. Together, these observations open an exciting new vista of understanding and therapeutic opportunity for this difficult and common disease.
阐明自身免疫性疾病中细胞因子产生的调节途径可能会导致新的治疗方法的发展。在此,我们综述了一些数据,这些数据表明 microRNAs(miRs)是一种调节活性,尤其强调了类风湿关节炎(RA)的发病机制。已经确定了一系列在 RA 患者关节腔内细胞亚群中失调的 miRs。它们在调节 RA 滑膜成纤维细胞的软骨侵袭表型方面起着关键作用。最近,几项研究表明,miRs 还调节白细胞的激活和细胞因子的产生,进而有助于效应性滑膜病理的免疫学成分。总的来说,这些观察结果为这种困难且常见的疾病提供了一个令人兴奋的新的理解和治疗机会。