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  • 标题:SARS-CoV-2 Infection Boosts MX1 Antiviral Effector in COVID-19 Patients
  • 本地全文:下载
  • 作者:Juan Bizzotto ; Pablo Sanchis ; Mercedes Abbate
  • 期刊名称:iScience
  • 印刷版ISSN:2589-0042
  • 出版年度:2020
  • 卷号:23
  • 期号:10
  • 页码:1-21
  • DOI:10.1016/j.isci.2020.101585
  • 语种:English
  • 出版社:Elsevier
  • 摘要:SummaryIn a published case-control study (GSE152075) from SARS-CoV-2-positive (n = 403) and -negative patients (n = 50), we analyzed the response to infection assessing gene expression of host cell receptors and antiviral proteins. The expression analysis associated with reported risk factors for COVID-19 was also assessed. SARS-CoV-2 cases had higherACE2, but lowerTMPRSS2,BSG/CD147,andCTSBexpression compared with negative cases. COVID-19 patients' age negatively affectedACE2expression.MX1andMX2were higher in COVID-19 patients. A negative trend forMX1andMX2was observed as patients' age increased. Principal-component analysis determined thatACE2,MX1,MX2, andBSG/CD147expression was able to cluster non-COVID-19 and COVID-19 individuals. Multivariable regression showed thatMX1expression significantly increased for each unit of viral load increment. Altogether, these findings support differences inACE2,MX1,MX2, andBSG/CD147expression between COVID-19 and non-COVID-19 patients and point out toMX1as a critical responder in SARS-CoV-2 infection.Graphical AbstractDisplay OmittedHighlights•COVID-19 patients present a distinct expression pattern for antiviral genes•MX1antiviral gene expression is triggered by SARS-CoV-2•MX1 can be induced by hemin, an FDA-approved drug•MX1 rises as a potential druggable targetHealth Informatics; Virology
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