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Plasma Gradient of Soluble Urokinase-Type Plasminogen Activator Receptor Is Linked to Pathogenic Plasma Proteome and Immune Transcriptome and Stratifies Outcomes in Severe COVID-19.

Authors :
Sarif J
Raychaudhuri D
D'Rozario R
Bandopadhyay P
Singh P
Mehta P
Hoque MA
Sinha BP
Kushwaha M
Sahni S
Devi P
Chattopadhyay P
Paul SR
Ray Y
Chaudhuri K
Banerjee S
Majumdar D
Saha B
Sarkar BS
Bhattacharya P
Chatterjee S
Paul S
Ghosh P
Pandey R
Sengupta S
Ganguly D
Source :
Frontiers in immunology [Front Immunol] 2021 Oct 28; Vol. 12, pp. 738093. Date of Electronic Publication: 2021 Oct 28 (Print Publication: 2021).
Publication Year :
2021

Abstract

Disease caused by SARS-CoV-2 coronavirus (COVID-19) led to significant morbidity and mortality worldwide. A systemic hyper-inflammation characterizes severe COVID-19 disease, often associated with acute respiratory distress syndrome (ARDS). Blood biomarkers capable of risk stratification are of great importance in effective triage and critical care of severe COVID-19 patients. Flow cytometry and next-generation sequencing were done on peripheral blood cells and urokinase-type plasminogen activator receptor (suPAR), and cytokines were measured from and mass spectrometry-based proteomics was done on plasma samples from an Indian cohort of COVID-19 patients. Publicly available single-cell RNA sequencing data were analyzed for validation of primary data. Statistical analyses were performed to validate risk stratification. We report here higher plasma abundance of suPAR, expressed by an abnormally expanded myeloid cell population, in severe COVID-19 patients with ARDS. The plasma suPAR level was found to be linked to a characteristic plasma proteome, associated with coagulation disorders and complement activation. Receiver operator characteristic curve analysis to predict mortality identified a cutoff value of suPAR at 1,996.809 pg/ml (odds ratio: 2.9286, 95% confidence interval 1.0427-8.2257). Lower-than-cutoff suPAR levels were associated with a differential expression of the immune transcriptome as well as favorable clinical outcomes, in terms of both survival benefit (hazard ratio: 0.3615, 95% confidence interval 0.1433-0.912) and faster disease remission in our patient cohort. Thus, we identified suPAR as a key pathogenic circulating molecule linking systemic hyperinflammation to the hypercoagulable state and stratifying clinical outcomes in severe COVID-19 patients with ARDS.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2021 Sarif, Raychaudhuri, D’Rozario, Bandopadhyay, Singh, Mehta, Hoque, Sinha, Kushwaha, Sahni, Devi, Chattopadhyay, Paul, Ray, Chaudhuri, Banerjee, Majumdar, Saha, Sarkar, Bhattacharya, Chatterjee, Paul, Ghosh, Pandey, Sengupta and Ganguly.)

Details

Language :
English
ISSN :
1664-3224
Volume :
12
Database :
MEDLINE
Journal :
Frontiers in immunology
Publication Type :
Academic Journal
Accession number :
34777349
Full Text :
https://doi.org/10.3389/fimmu.2021.738093