Department of Musculoskeletal Biology, MRC Arthritis Research UK Centre for Integrated Research into Musculoskeletal Ageing, Institute of Ageing and Chronic Disease, University of Liverpool, Liverpool, UK.
Ann Rheum Dis. 2015 Jul;74(7):1340-6. doi: 10.1136/annrheumdis-2014-207172. Epub 2015 Apr 28.
The idiopathic inflammatory myopathies (IIMs) are a group of rare autoimmune disorders, collectively known as myositis. Affected patients present with proximal muscle weakness, which usually improves following treatment with immunosuppressants, but often incompletely so, thus many patients remain weak. IIMs are characterised histologically by inflammatory cell infiltrates into skeletal muscle and overexpression of major histocompatibility complex I on muscle cell surfaces. Although inflammatory cell infiltrates represent a major feature of myositis there is growing evidence that muscle weakness correlates only poorly with the degree of cellular infiltration, while weakness may in fact precede such infiltrations. The mechanisms underpinning such non-immune cell mediated weakness in IIM are poorly understood. Activation of the endoplasmic reticulum stress pathways appears to be a potential contributor. Data from non-muscle cells indicate that endoplasmic reticulum stress results in altered redox homeostasis capable of causing oxidative damage. In myopathological situations other than IIM, as seen in ageing and sepsis, evidence supports an important role for reactive oxygen species (ROS). Modified ROS generation is associated with mitochondrial dysfunction, depressed force generation and activation of muscle catabolic and autophagy pathways. Despite the growing evidence demonstrating a key role for ROS in skeletal muscle dysfunction in myopathologies other than IIM, no research has yet investigated the role of modified generation of ROS in inducing the weakness characteristic of IIM. This article reviews current knowledge regarding muscle weakness in the absence of immune cells in IIM, and provides a background to the potential role of modified ROS generation as a mechanism of muscle dysfunction. The authors suggest that ROS-mediated mechanisms are potentially involved in non-immune cell mediated weakness seen in IIM and outline how these mechanisms might be investigated in this context. This appears a timely strategy, given recent developments in targeted therapies which specifically modify ROS generation.
特发性炎性肌病(IIM)是一组罕见的自身免疫性疾病,统称为肌炎。受影响的患者表现为进行性肌无力,通常在免疫抑制剂治疗后会有所改善,但往往改善不完全,因此许多患者仍存在肌无力。IIM 在组织学上的特征是炎症细胞浸润骨骼肌和主要组织相容性复合体 I 在肌肉细胞膜表面的过度表达。尽管炎症细胞浸润是肌炎的主要特征,但越来越多的证据表明,肌肉无力与细胞浸润的程度相关性很差,而肌无力实际上可能先于这种浸润。IIM 中非免疫细胞介导的肌无力的机制尚不清楚。内质网应激途径的激活似乎是一个潜在的贡献因素。来自非肌肉细胞的数据表明,内质网应激会导致氧化还原稳态改变,从而导致氧化损伤。在除 IIM 以外的肌肉病理情况下,如衰老和败血症中,有证据支持活性氧(ROS)的重要作用。ROS 生成的改变与线粒体功能障碍、肌力生成减少以及肌肉分解代谢和自噬途径的激活有关。尽管越来越多的证据表明 ROS 在除 IIM 以外的肌肉病变中的骨骼肌功能障碍中起着关键作用,但目前还没有研究调查 ROS 生成的改变在诱导 IIM 特征性肌无力中的作用。本文综述了 IIM 中无免疫细胞时肌肉无力的现有知识,并为 ROS 生成的改变作为肌肉功能障碍的机制提供了背景。作者提出,ROS 介导的机制可能与 IIM 中非免疫细胞介导的肌无力有关,并概述了在这种情况下如何研究这些机制。鉴于最近针对特定 ROS 生成的靶向治疗的发展,这似乎是一种及时的策略。