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A dynamic mucin mRNA signature associates with COVID-19 disease presentation and severity

Authors :
Annemieke Smet
Tom Breugelmans
Johan Michiels
Kevin Lamote
Wout Arras
Joris G. De Man
Leo Heyndrickx
Anne Hauner
Manon Huizing
Surbhi Malhotra-Kumar
Martin Lammens
An Hotterbeekx
Samir Kumar-Singh
Aline Verstraeten
Bart Loeys
Veronique Verhoeven
Rita Jacobs
Karolien Dams
Samuel Coenen
Kevin K. Ariën
Philippe G. Jorens
Benedicte Y. De Winter
Source :
JCI Insight, Vol 6, Iss 19 (2021)
Publication Year :
2021
Publisher :
American Society for Clinical investigation, 2021.

Abstract

BACKGROUND SARS-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.METHODS Using 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.RESULTS We 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.CONCLUSION This 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.FUNDING The Antwerp University Research and the Research Foundation Flanders COVID-19 funds.

Subjects

Subjects :
COVID-19
Medicine

Details

Language :
English
ISSN :
23793708
Volume :
6
Issue :
19
Database :
Directory of Open Access Journals
Journal :
JCI Insight
Publication Type :
Academic Journal
Accession number :
edsdoj.fdefd6254314adea1d02c9168043878
Document Type :
article
Full Text :
https://doi.org/10.1172/jci.insight.151777