Type I Interferons in Systemic Autoimmune Rheumatic Diseases: Pathogenesis, Clinical Features and Treatment Options.

Q4 Medicine Mediterranean Journal of Rheumatology Pub Date : 2024-06-30 eCollection Date: 2024-06-01 DOI:10.31138/mjr.270324.tis
Konstantinos Drougkas, Charalampos Skarlis, Clio Mavragani
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Abstract

Type I interferon (IFN) pathway dysregulation plays a crucial role in the pathogenesis of several systemic autoimmune rheumatic diseases (SARDs), including systemic lupus erythematosus (SLE), Sjögren's disease (SjD), systemic sclerosis (SSc), dermatomyositis (DM) and rheumatoid arthritis (RA). Genetic and epigenetic alterations have been involved in dysregulated type I IFN responses in systemic autoimmune disorders. Aberrant type I IFN production and secretion have been associated with distinct clinical phenotypes, disease activity, and severity as well as differentiated treatment responses among SARDs. In this review, we provide an overview of the role of type I IFNs in systemic autoimmune diseases including SLE, RA, SjD, SSc, and DM focusing on pathophysiological, clinical, and therapeutical aspects.

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系统性自身免疫性风湿病中的 I 型干扰素:发病机制、临床特征和治疗方案。
I型干扰素(IFN)通路失调在多种系统性自身免疫性风湿病(SARDs)的发病机制中起着至关重要的作用,包括系统性红斑狼疮(SLE)、斯约格伦病(SjD)、系统性硬化症(SSc)、皮肌炎(DM)和类风湿性关节炎(RA)。遗传和表观遗传的改变与系统性自身免疫性疾病中失调的 I 型 IFN 反应有关。I 型 IFN 的产生和分泌异常与不同的临床表型、疾病活动性和严重程度以及系统性自身免疫性疾病之间不同的治疗反应有关。在这篇综述中,我们概述了 I 型FN 在系统性自身免疫疾病(包括系统性红斑狼疮、关节炎、SjD、SSc 和 DM)中的作用,重点关注病理生理学、临床和治疗方面。
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CiteScore
2.00
自引率
0.00%
发文量
42
审稿时长
8 weeks
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