Jagot Ferdinand, Davoust Nathalie
Département de biologie, École Normale Supérieure de Lyon, France.
Département de biologie, École Normale Supérieure de Lyon, France - Laboratoire de biologie et de modélisation de la cellule, UMR5239/École Normale Supérieure de Lyon, UMS 344 Biosciences Lyon Gerland, université de Lyon, France.
Med Sci (Paris). 2017 Jun-Jul;33(6-7):620-628. doi: 10.1051/medsci/20173306019. Epub 2017 Jul 19.
Multiple sclerosis (MS) is an auto-immune demyelinating disorder characterized by a chronic neuro-inflammatory process associated with an infiltration of the central nervous system (CNS) by autoreactive lymphocytes. The etiology of the disease remains unclear but the recent discovery of a dysregulated miRNA network in both cells and extracellular fluids of MS patients has brought new insights on the pathophysiological mechanisms involved in this disorder. miRNAs can induce a T cell polarization towards a pathological Th17 or Th1 phenotype and a deleterious activation of microglia, the CNS-resident macrophages. We provide here a review of the most recent data regarding miRNA dysregulation and pathophysiological roles in MS patients and in the animal model of MS, EAE (experimental autoimmune encephalomyelitis). Moreover, we discuss the putative clinical value of miRNAs as a novel biomarker and diagnostic tool for MS.
多发性硬化症(MS)是一种自身免疫性脱髓鞘疾病,其特征是慢性神经炎症过程,伴有自身反应性淋巴细胞浸润中枢神经系统(CNS)。该疾病的病因尚不清楚,但最近在MS患者的细胞和细胞外液中发现了失调的miRNA网络,这为该疾病所涉及的病理生理机制带来了新的见解。miRNA可诱导T细胞向病理性Th17或Th1表型极化,并激活小胶质细胞(中枢神经系统驻留巨噬细胞),产生有害作用。我们在此综述了有关MS患者和MS动物模型EAE(实验性自身免疫性脑脊髓炎)中miRNA失调及其病理生理作用的最新数据。此外,我们还讨论了miRNA作为MS新型生物标志物和诊断工具的潜在临床价值。