Patients with severe COVID-19 do not have elevated autoantibodies against common diagnostic autoantigens

Antigona Ulndreaj, Mingyue Wang, S. Misaghian, L. Paone, G. Sigal, M. Stengelin, C. Campbell, Logan R. Van Nynatten, A. Soosaipillai, Atefeh Ghorbani, A. Mathew, D. Fraser, E. Diamandis, I. Prassas
{"title":"Patients with severe COVID-19 do not have elevated autoantibodies against common diagnostic autoantigens","authors":"Antigona Ulndreaj, Mingyue Wang, S. Misaghian, L. Paone, G. Sigal, M. Stengelin, C. Campbell, Logan R. Van Nynatten, A. Soosaipillai, Atefeh Ghorbani, A. Mathew, D. Fraser, E. Diamandis, I. Prassas","doi":"10.1515/cclm-2022-0239","DOIUrl":null,"url":null,"abstract":"Abstract Objectives Infection by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), the causative pathogen of coronavirus disease 2019 (COVID-19) presents occasionally with an aberrant autoinflammatory response, including the presence of elevated circulating autoantibodies in some individuals. Whether the development of autoantibodies against self-antigens affects COVID-19 outcomes remains unclear. To better understand the prognostic role of autoantibodies in COVID-19, we quantified autoantibodies against 23 markers that are used for diagnosis of autoimmune disease. To this end, we used serum samples from patients with severe [intensive care unit (ICU)] and moderate (ward) COVID-19, across two to six consecutive time points, and compared autoantibody levels to uninfected healthy and ICU controls. Methods Acute and post-acute serum (from 1 to 26 ICU days) was collected from 18 ICU COVID-19-positive patients at three to six time points; 18 ICU COVID-19-negative patients (sampled on ICU day 1 and 3); 21 ward COVID-19-positive patients (sampled on hospital day 1 and 3); and from 59 healthy uninfected controls deriving from two cohorts. Levels of IgG autoantibodies against 23 autoantigens, commonly used for autoimmune disease diagnosis, were measured in serum samples using MSD® U-PLEX electrochemiluminescence technology (MSD division Meso Scale Discovery®), and results were compared between groups. Results There were no significant elevations of autoantibodies for any of the markers tested in patients with severe COVID-19. Conclusions Sample collections at longer time points should be considered in future studies, for assessing the possible development of autoantibody responses following infection with SARS-CoV-2.","PeriodicalId":10388,"journal":{"name":"Clinical Chemistry and Laboratory Medicine (CCLM)","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2022-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Chemistry and Laboratory Medicine (CCLM)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1515/cclm-2022-0239","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3

Abstract

Abstract Objectives Infection by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), the causative pathogen of coronavirus disease 2019 (COVID-19) presents occasionally with an aberrant autoinflammatory response, including the presence of elevated circulating autoantibodies in some individuals. Whether the development of autoantibodies against self-antigens affects COVID-19 outcomes remains unclear. To better understand the prognostic role of autoantibodies in COVID-19, we quantified autoantibodies against 23 markers that are used for diagnosis of autoimmune disease. To this end, we used serum samples from patients with severe [intensive care unit (ICU)] and moderate (ward) COVID-19, across two to six consecutive time points, and compared autoantibody levels to uninfected healthy and ICU controls. Methods Acute and post-acute serum (from 1 to 26 ICU days) was collected from 18 ICU COVID-19-positive patients at three to six time points; 18 ICU COVID-19-negative patients (sampled on ICU day 1 and 3); 21 ward COVID-19-positive patients (sampled on hospital day 1 and 3); and from 59 healthy uninfected controls deriving from two cohorts. Levels of IgG autoantibodies against 23 autoantigens, commonly used for autoimmune disease diagnosis, were measured in serum samples using MSD® U-PLEX electrochemiluminescence technology (MSD division Meso Scale Discovery®), and results were compared between groups. Results There were no significant elevations of autoantibodies for any of the markers tested in patients with severe COVID-19. Conclusions Sample collections at longer time points should be considered in future studies, for assessing the possible development of autoantibody responses following infection with SARS-CoV-2.
重症COVID-19患者针对常见诊断性自身抗原的自身抗体未升高
【摘要】目的冠状病毒病2019 (COVID-19)的病原——严重急性呼吸综合征冠状病毒-2 (SARS-CoV-2)感染偶尔会出现异常的自身炎症反应,包括部分个体存在循环自身抗体升高。针对自身抗原的自身抗体的产生是否会影响COVID-19的结局尚不清楚。为了更好地了解自身抗体在COVID-19中的预后作用,我们对用于自身免疫性疾病诊断的23种标志物的自身抗体进行了量化。为此,我们使用了重症[ICU]和中度(病房)COVID-19患者连续2至6个时间点的血清样本,并将自身抗体水平与未感染的健康和ICU对照进行比较。方法采集18例ICU covid -19阳性患者3 ~ 6个时间点急性及急性后血清(1 ~ 26 ICU d);ICU covid -19阴性患者18例(在ICU第1天和第3天取样);21例病区covid -19阳性患者(住院第1天和第3天取样);以及来自两个队列的59名健康未感染对照。采用MSD®U-PLEX电化学发光技术(MSD division Meso Scale Discovery®)检测血清样本中针对23种自身抗原的IgG自身抗体水平,并比较两组结果。结果重症COVID-19患者各项指标自身抗体均无明显升高。结论在未来的研究中应考虑在更长的时间点采集样本,以评估感染SARS-CoV-2后可能出现的自身抗体反应。
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 求助全文
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信