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类风湿关节炎中的基因、环境、微生物群与黏膜免疫耐受

Gene, environment, microbiome and mucosal immune tolerance in rheumatoid arthritis.

作者信息

Catrina Anca I, Deane Kevin D, Scher Jose U

机构信息

Rheumatology Unit, Department of Medicine, Karolinska University Hospital and Institutet, Stockholm, Sweden,

Division of Rheumatology, University of Colorado, School of Medicine, Aurora, CO and.

出版信息

Rheumatology (Oxford). 2016 Mar;55(3):391-402. doi: 10.1093/rheumatology/keu469. Epub 2014 Dec 23.

Abstract

RA is a complex multifactorial chronic disease that transitions through several stages. Multiple studies now support that there is a prolonged phase in early RA development during which there is serum elevation of RA-related autoantibodies including RF and ACPAs in the absence of clinically evident synovitis. This suggests that RA pathogenesis might originate in an extra-articular location, which we hypothesize is a mucosal site. In discussing this hypothesis, we will present herein the current understanding of mucosal immunology, including a discussion about the generation of autoimmune responses at these surfaces. We will also examine how other factors such as genes, microbes and other environmental toxins (including tobacco smoke) could influence the triggering of autoimmunity at mucosal sites and eventually systemic organ disease. We will also propose a research agenda to improve our understanding of the role of mucosal inflammation in the development of RA.

摘要

类风湿关节炎(RA)是一种复杂的多因素慢性疾病,经历多个阶段。现在多项研究支持,在早期类风湿关节炎发展过程中有一个延长阶段,在此期间,在没有临床明显滑膜炎的情况下,类风湿关节炎相关自身抗体(包括类风湿因子(RF)和抗环瓜氨酸肽抗体(ACPA))的血清水平会升高。这表明类风湿关节炎的发病机制可能起源于关节外部位,我们推测是一个黏膜部位。在讨论这一假说时,我们将在此介绍对黏膜免疫学的当前认识,包括对这些表面自身免疫反应产生的讨论。我们还将研究其他因素,如基因、微生物和其他环境毒素(包括烟草烟雾)如何影响黏膜部位自身免疫的触发以及最终的全身器官疾病。我们还将提出一项研究议程,以增进我们对黏膜炎症在类风湿关节炎发展中作用的理解。

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