IgA血管炎和川崎病患者显示干扰素信号失调

IF 2 4区 医学 Q2 RHEUMATOLOGY
Sevki Erdem Varol, Cisem Cinar, Nihan Burtecene, Sezgin Sahin, Mehmet Yildiz, Kenan Barut, Haluk Cokugras, Sinem Firtina, Ozgur Kasapcopur, Ayca Kiykim
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引用次数: 0

摘要

目的IgA血管炎(IgAV)和川崎病(KD)是儿童最常见的血管炎。尽管病毒感染、遗传因素和环境因素等多种因素参与了这两种疾病的发展,但其发病机制尚不清楚。干扰素(IFN)信号反映了I型IFN信号通路的激活,是一种诊断和预后工具,对自身免疫性疾病的发病机制和治疗有重要贡献。在我们的研究中,我们旨在探讨IFN信号在IgAV和KD患者中的作用。材料与方法纳入32例IgAV患儿和4例KD患儿。分析所有受试者血清样本中IL-1、IL-6、IL-8、IL-10、IL-17、IL-18、TNF-α、TNF- r1、TNF- r2和IFN- γ水平,并检测患者和健康对照(n = 26)中IFN相关基因(STAT1、IFI27、IFI44、IFI44L、IFIT1和RSAD2)的表达,采用RT-PCR方法计算IFN评分。结果与对照组相比,IgAV和KD患者中3个基因(IFIT1、IFI44和IFI27)的表达显著增加,另外3个基因(RSAD2、STAT1和IFI44L)的表达显著降低。IFN评分(IFN > 3)在胃肠道受累患者、需要皮质类固醇治疗的患者和必须住院的患者中均显著升高。在肾脏受累和未受累的患者中,IFN水平无显著差异。IgAV伴有胃肠道症状的患者血清IL-1水平明显升高。诊断为KD的4例患者中有3例IFN评分较高。结论与对照组相比,IgAV和KD患者存在1型IFN信号失调。胃肠道受累的风险明显增加,需要皮质类固醇治疗,并且在诊断为IgAV且IFN水平高的患者中观察到住院治疗。这强调了IFN评分可以作为一个关键的预测指标的观点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Patients With IgA Vasculitis and Kawasaki Disease Show Dysregulated Interferon Signature

Patients With IgA Vasculitis and Kawasaki Disease Show Dysregulated Interferon Signature

Objective

IgA vasculitis (IgAV) and Kawasaki disease (KD) are the most common forms of childhood vasculitis. Although various factors such as viral infections, genetic factors, and environmental factors are involved in the development of both diseases, their pathogenesis remains unclear. The interferon (IFN) signature, which reflects the activation of type I IFN signaling pathways, is a diagnostic and prognostic tool that contributes significantly to the pathogenesis and management of autoimmune diseases. In our study, we aimed to investigate the role of the IFN signature in patients with IgAV and KD.

Material and Methods

Thirty-two children with IgAV and four patients diagnosed with KD were included in the study. Serum levels of IL-1, IL-6, IL-8, IL-10, IL-17, IL-18, TNF-α, TNF-R1, TNF-R2, and IFN-gamma were analyzed in the serum samples of all participants, and the expression of IFN-related genes (STAT1, IFI27, IFI44, IFI44L, IFIT1, and RSAD2) was assessed in the patients and healthy controls (n = 26) to calculate the IFN score by RT-PCR method.

Results

A significant increase in the expression of three genes (IFIT1, IFI44, and IFI27) and decreased expression of the other three genes (RSAD2, STAT1, and IFI44L) was found in patients with IgAV and KD compared to the control group. Significantly higher IFN scores (IFN > 3) were found in patients with gastrointestinal involvement, in patients who required corticosteroid therapy, and in patients who had to be hospitalized. No significant difference in IFN levels was found between patients with and without renal involvement. Significantly higher serum IL-1 levels were found in patients with gastrointestinal symptoms with IgAV. High IFN scores were found in three out of four patients diagnosed with KD.

Conclusion

A dysregulated type 1 IFN signature was found in patients with IgAV and KD compared to the control group. A significantly increased risk of gastrointestinal involvement required corticosteroid therapy, and hospitalization was observed in patients diagnosed with IgAV who had high IFN levels. This underlines the idea that the IFN score could serve as a crucial prognostic indicator.

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来源期刊
CiteScore
3.70
自引率
4.00%
发文量
362
审稿时长
1 months
期刊介绍: The International Journal of Rheumatic Diseases (formerly APLAR Journal of Rheumatology) is the official journal of the Asia Pacific League of Associations for Rheumatology. The Journal accepts original articles on clinical or experimental research pertinent to the rheumatic diseases, work on connective tissue diseases and other immune and allergic disorders. The acceptance criteria for all papers are the quality and originality of the research and its significance to our readership. Except where otherwise stated, manuscripts are peer reviewed by two anonymous reviewers and the Editor.
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