Dipartimento di Scienze Cliniche e Molecolari, Università Politecnica delle Marche, and Clinica Medica, Ospedali Riuniti, Ancona, Italy.
Clin Exp Rheumatol. 2013 Mar-Apr;31(2 Suppl 76):3-7. Epub 2013 Jul 22.
Systemic sclerosis or scleroderma (SSc) is a clinically heterogeneous disease of the connective tissue characterised by vascular, immune/inflammatory and fibrotic manifestations. Despite extensive investigations, the key pathogenic links between these disease hallmarks remain obscure, as well as the etiology underlying the beginning of this complex disorder. As for other diseases characterised by prominent autoimmune phenomena, the search for infectious agents responsible for immune tolerance breaks or molecular mimicry events has been a long-pursued issue. In this review, we summarise the current knowledge regarding the association of different viral infections with SSc, focusing mainly on those reports describing a mechanistic interplay between the viral agents and the pathogenesis of SSc. Moreover, we speculate on how viral infections may trigger additional pathogenic mechanisms recently proposed to contributing to SSc phenotype.
系统性硬化症或硬皮病(SSc)是一种临床异质性的结缔组织疾病,其特征为血管、免疫/炎症和纤维化表现。尽管进行了广泛的研究,但这些疾病特征之间的关键致病联系以及这种复杂疾病开始的病因仍然不清楚。对于其他以明显自身免疫现象为特征的疾病,寻找导致免疫耐受破坏或分子模拟事件的传染性病原体一直是一个长期追求的问题。在这篇综述中,我们总结了目前关于不同病毒感染与 SSc 相关性的知识,主要集中在那些描述病毒因子与 SSc 发病机制之间的机制相互作用的报告。此外,我们推测病毒感染如何触发最近提出的可能导致 SSc 表型的其他致病机制。