Levels of type I interferon in patients with systemic lupus erythematosus

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
{"title":"Levels of type I interferon in patients with systemic lupus erythematosus","authors":"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","doi":"10.47196/rar.v32i1.365","DOIUrl":null,"url":null,"abstract":"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.\nObjectives: 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.\nResults: 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).\nConclusions: these results suggest the importance that the determination of IFN type I could have for the monitoring of SLE activity.","PeriodicalId":249076,"journal":{"name":"Revista Argentina de Reumatología","volume":"1 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Revista Argentina de Reumatología","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.47196/rar.v32i1.365","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

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.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
系统性红斑狼疮患者的I型干扰素水平
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。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Insuficiencia suprarrenal aguda secundaria a hemorragia adrenal espontánea por síndrome antifosfolipídico: serie de casos Linfoma y granulomatosis eosinofílica con poliangeitis (síndrome de Churg-Strauss): reporte de un caso Linfoma y granulomatosis eosinofílica con poliangeitis (síndrome de Churg-Strauss): reporte de un caso Insuficiencia suprarrenal aguda secundaria a hemorragia adrenal espontánea por síndrome antifosfolipídico: serie de casos Características de los pacientes con artritis reumatoide que impactan en la satisfacción y la adherencia al tratamiento: subanálisis de los datos de Argentina, Chile y Uruguay del estudio SENSE
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1