系统性红斑狼疮患者的I型干扰素水平

C. Erramuspe, M. Racca, M. Siemsen, M. Pelosso, M. Quaglia, Y. Tissera, C. Alonso, V. Savio, J. Albiero, C. Gobbi, P. Alba, L. Boffelli, M. Maccioni, M. Demarchi
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引用次数: 0

摘要

I型干扰素(IFN)是一种细胞因子,在系统性红斑狼疮(SLE)的发病机制中起着重要作用。不同水平的细胞因子可以解释这种病理的异质性,并有助于评估其活性。目的:确定SLE患者血清I型IFN水平,并评估其作为活性生物标志物的有效性。材料和方法:16例SLE患者(ACR 1997)和16例对照。方法:疾病活动性(SLEDAI-2K)、器官损害(SLICC)、I型IFN (HEK-Blue- IFNα/β)、抗dsdna抗体(间接免疫荧光)、抗ena抗体(ELISA)、C3-C4(免疫比浊法)。统计:InfoStat / Instat / MedCalc。P值<0.05,差异有统计学意义。结果:SLE组IFN浓度较对照组升高(p <0.05)。IFN值高于临界值的患者与存在抗dsdna抗体相关(OR: 13.33;p < 0.05)。补体不足患者和SLEDAI-2K评分大于8的患者IFN水平分别高于补体正常患者和指数评分较低的患者(p<0.05)。结论:这些结果提示了IFN I型的测定对SLE活动监测的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Levels of type I interferon in patients with systemic lupus erythematosus
Introduction: type I interferon (IFN) is a cytokine that plays a fundamental role in the pathogenesis of Systemic Lupus Erythematosus (SLE). Different levels of this cytokine could explain the heterogeneity of this pathology and be useful to evaluate its activity. Objectives: to determine the serum type I IFN levels in patients with SLE and evaluate its usefulness as a biomarker of activity. Material and Method: 16 patients with SLE (ACR 1997) and 16 controls. Methods: Disease activity (SLEDAI-2K), organ damage (SLICC), type I IFN (HEK-Blue- IFNα/β), anti-dsDNA antibodies (Indirect Immunofluorescence), anti-ENA antibodies (ELISA), C3-C4 (Immunoturbidimetry). Statistics: InfoStat/Instat/MedCalc. P values <0.05 were statistically significant. Results: an increase in IFN concentration was observed in the SLE group respect to the control (p <0.05). Patients with IFN values above the cut-off point were associated with the presence of anti-dsDNA antibodies (OR: 13.33; p<0.05). Hypocomplementemic patients and those with a SLEDAI-2K score greater than 8 had higher IFN levels compared to patients with normal complement and a lower index score, respectively (p<0.05). Conclusions: these results suggest the importance that the determination of IFN type I could have for the monitoring of SLE activity.
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