Fucosylated N-glycans as early biomarkers of COVID-19 severity

The pathological mechanisms of SARS-CoV-2 in humans remain unclear and the unpredictability of COVID-19 progression may be attributed to the absence of biomarkers that contribute to the prognosis of this disease. Therefore, the discovery of biomarkers is needed for reliable risk stratification and t...

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Published inFrontiers in immunology Vol. 14; p. 1204661
Main Authors Paton, Beatrix, Herrero, Pol, Peraire, Joaquim, del Pino, Antoni, Chafino, Silvia, Martinez-Picado, Javier, Gómez-Bertomeu, Fréderic, Rull, Anna, Canela, Núria, Suárez, Manuel
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 05.06.2023
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ISSN1664-3224
1664-3224
DOI10.3389/fimmu.2023.1204661

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Summary:The pathological mechanisms of SARS-CoV-2 in humans remain unclear and the unpredictability of COVID-19 progression may be attributed to the absence of biomarkers that contribute to the prognosis of this disease. Therefore, the discovery of biomarkers is needed for reliable risk stratification and to identify patients who are more likely to progress to a critical stage. Aiming to identify new biomarkers we analysed N-glycan traits in plasma from 196 patients with COVID-19. Samples were classified into three groups according to their severity (mild, severe and critical) and obtained at diagnosis (baseline) and at 4 weeks of follow-up (postdiagnosis), to evaluate their behaviour through disease progression. N-glycans were released with PNGase F and labelled with Rapifluor-MS, followed by their analysis by LC-MS/MS. The Simglycan structural identification tool and Glycostore database were employed to predict the structure of glycans. We determined that plasma from SARS-CoV-2-infected patients display different N-glycosylation profiles depending on the disease severity. Specifically, levels of fucosylation and galactosylation decreased with increasing severity and Fuc1Hex5HexNAc5 was identified as the most suitable biomarker to stratify patients at diagnosis and distinguish mild from critical outcomes. In this study we explored the global plasma glycosignature, reflecting the inflammatory state of the organs during the infectious disease. Our findings show the promising potential of glycans as biomarkers of COVID-19 severity.
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Reviewed by: Jennifer Serwanga, Uganda Virus Research Institute (UVRI), Uganda; Valeria De Giorgi, National Institutes of Health (NIH), United States
Edited by: Prof. Pei-Hui Wang, Shandong University, China
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2023.1204661