Total plasma N-glycomic patterns of COVID-19 disease

Total plasma N-glycans alter in disease states, with few studies focused on COVID-19. A discovery cohort of 310 COVID-19 patients, replicated with 97 COVID-19 patients and tested with 100 COVID-19 patients, was used to unearth the N-glycans capable of distinguishing infection, as well as prognosis of intensive care unit (ICU) admission and mortality. All significant bisected glycans were decreased in patients compared to controls, whilst fucosylated tri-antennary glycans and sialylated tetra-antennary glycans were increased in patients. For both those admitted to the ICU and those who died, Peak 61 (A4G4S4F) was elevated in the more severe disease course, while Peak 29 (FA2G2S2) was lowered. Pinpointing specific glycosylation changes has alluded to a potential story of glycoprotein pathways in response to SARS-CoV-2 infection. This study could be further explored through deriving the glycoproteins associated with the glycans of interest and the glycosylation changes experienced on these proteins.

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Publication Details

Journal
Glycoconjugate Journal
Published
2026-01-20
DOI
https://doi.org/10.1007/s10719-025-10201-1
Primary Topic
Glycosylation and Glycoproteins Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Total plasma N-glycomic patterns of COVID-19 disease

Patrick Mallon, Marco P. Monopoli, Jack Cheeseman, Thomas Sénard et al.
Glycoconjugate Journal
Glycosylation and Glycoproteins Research
article

Total plasma N-glycomic patterns of COVID-19 disease

Patrick Mallon, Marco P. Monopoli, Jack Cheeseman, Thomas Sénard, Oleg A. Mayboroda, Georgia Elgood-Hunt, Daryl L. Fernandes, Cormac McCarthy, Richard A. Gardner, Craig P. Thompson, Paulina A. Urbanowicz, Alejandro A. Garcia Leon
article en

Abstract

Total plasma N-glycans alter in disease states, with few studies focused on COVID-19. A discovery cohort of 310 COVID-19 patients, replicated with 97 COVID-19 patients and tested with 100 COVID-19 patients, was used to unearth the N-glycans capable of distinguishing infection, as well as prognosis of intensive care unit (ICU) admission and mortality. All significant bisected glycans were decreased in patients compared to controls, whilst fucosylated tri-antennary glycans and sialylated tetra-antennary glycans were increased in patients. For both those admitted to the ICU and those who died, Peak 61 (A4G4S4F) was elevated in the more severe disease course, while Peak 29 (FA2G2S2) was lowered. Pinpointing specific glycosylation changes has alluded to a potential story of glycoprotein pathways in response to SARS-CoV-2 infection. This study could be further explored through deriving the glycoproteins associated with the glycans of interest and the glycosylation changes experienced on these proteins.

Glycoconjugate JournalVol. 43(1)
University College Dublin (IE), Royal College of Surgeons in Ireland (IE), Leiden University Medical Center (NL), University of Warwick (GB), Netherlands Metabolomics Centre (NL), St. Vincent's University Hospital (IE), Azienda USL di Bologna (IT), Ludger (United Kingdom) (GB)
University Hospitals Coventry and Warwickshire NHS Trust
Good health and well-being
Openalex Percentile: Top 84%
Glycosylation and Glycoproteins Research
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