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A dynamic mucin mRNA signature associates with COVID-19 disease presentation and severity.
Smet, Annemieke; Breugelmans, Tom; Michiels, Johan; Lamote, Kevin; Arras, Wout; De Man, Joris G; Heyndrickx, Leo; Hauner, Anne; Huizing, Manon; Malhotra-Kumar, Surbhi; Lammens, Martin; Hotterbeekx, An; Kumar-Singh, Samir; Verstraeten, Aline; Loeys, Bart; Verhoeven, Veronique; Jacobs, Rita; Dams, Karolien; Coenen, Samuel; Ariën, Kevin K; Jorens, Philippe G; De Winter, Benedicte Y.
  • Smet A; Laboratory of Experimental Medicine and Pediatrics, Faculty of Medicine and Health Sciences, and.
  • Breugelmans T; Infla-med, Centre of Excellence, University of Antwerp, Antwerp, Belgium.
  • Michiels J; Laboratory of Experimental Medicine and Pediatrics, Faculty of Medicine and Health Sciences, and.
  • Lamote K; Infla-med, Centre of Excellence, University of Antwerp, Antwerp, Belgium.
  • Arras W; Virology Unit, Institute of Tropical Medicine Antwerp, Antwerp, Belgium.
  • De Man JG; Laboratory of Experimental Medicine and Pediatrics, Faculty of Medicine and Health Sciences, and.
  • Heyndrickx L; Infla-med, Centre of Excellence, University of Antwerp, Antwerp, Belgium.
  • Hauner A; Internal Medicine and Pediatrics, Ghent University, Ghent, Belgium.
  • Huizing M; Laboratory of Experimental Medicine and Pediatrics, Faculty of Medicine and Health Sciences, and.
  • Malhotra-Kumar S; Infla-med, Centre of Excellence, University of Antwerp, Antwerp, Belgium.
  • Lammens M; Laboratory of Experimental Medicine and Pediatrics, Faculty of Medicine and Health Sciences, and.
  • Hotterbeekx A; Infla-med, Centre of Excellence, University of Antwerp, Antwerp, Belgium.
  • Kumar-Singh S; Virology Unit, Institute of Tropical Medicine Antwerp, Antwerp, Belgium.
  • Verstraeten A; Virology Unit, Institute of Tropical Medicine Antwerp, Antwerp, Belgium.
  • Loeys B; Biobank Antwerpen, Antwerp University Hospital, Edegem, Belgium.
  • Verhoeven V; Laboratory of Medical Microbiology, Vaccine and Infectious Disease Institute, Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.
  • Jacobs R; Department of Histopathology, Antwerp University Hospital, Edegem, Belgium.
  • Dams K; Laboratory of Cell Biology and Histology, Molecular Pathology Group, Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.
  • Coenen S; Laboratory of Cell Biology and Histology, Molecular Pathology Group, Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.
  • Ariën KK; Center of Medical Genetics, University of Antwerp and Antwerp University Hospital, Antwerp, Belgium.
  • Jorens PG; Center of Medical Genetics, University of Antwerp and Antwerp University Hospital, Antwerp, Belgium.
  • De Winter BY; Department of Family Medicine and Population Health, Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.
JCI Insight ; 6(19)2021 10 08.
Article in English | MEDLINE | ID: covidwho-1376547
ABSTRACT
BACKGROUNDSARS-CoV-2 infection induces mucin overexpression, further promoting disease. Given that mucins are critical components of innate immunity, unraveling their expression profiles that dictate the course of disease could greatly enhance our understanding and management of COVID-19.METHODSUsing validated RT-PCR assays, we assessed mucin mRNA expression in the blood of patients with symptomatic COVID-19 compared with symptomatic patients without COVID-19 and healthy controls and correlated the data with clinical outcome parameters. Additionally, we analyzed mucin expression in mucus and lung tissue from patients with COVID-19 and investigated the effect of drugs for COVID-19 treatment on SARS-CoV-2-induced mucin expression in pulmonary epithelial cells.RESULTSWe identified a dynamic blood mucin mRNA signature that clearly distinguished patients with symptomatic COVID-19 from patients without COVID-19 based on expression of MUC1, MUC2, MUC4, MUC6, MUC13, MUC16, and MUC20 (AUCROC of 91.8%; sensitivity and specificity of 90.6% and 93.3%, respectively) and that discriminated between mild and critical COVID-19 based on the expression of MUC16, MUC20, and MUC21 (AUCROC of 89.1%; sensitivity and specificity of 90.0% and 85.7%, respectively). Differences in the transcriptional landscape of mucins in critical cases compared with mild cases identified associations with COVID-19 symptoms, respiratory support, organ failure, secondary infections, and mortality. Furthermore, we identified different mucins in the mucus and lung tissue of critically ill COVID-19 patients and showed the ability of baricitinib, tocilizumab, favipiravir, and remdesivir to suppress expression of SARS-CoV-2-induced mucins.CONCLUSIONThis multifaceted blood mucin mRNA signature showed the potential role of mucin profiling in diagnosing, estimating severity, and guiding treatment options in patients with COVID-19.FUNDINGThe Antwerp University Research and the Research Foundation Flanders COVID-19 funds.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: RNA, Messenger / COVID-19 / Mucins Type of study: Diagnostic study / Observational study / Prognostic study Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: English Year: 2021 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: RNA, Messenger / COVID-19 / Mucins Type of study: Diagnostic study / Observational study / Prognostic study Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: English Year: 2021 Document Type: Article