The Glycosylation of Serum IgG Antibodies in Post-COVID-19 and Post-Vaccination Patients.

Publication date: Jan 18, 2025

The signature of human serum IgG glycosylation is critical in the defense against pathogens. Alterations of IgG N-glycome were associated with COVID-19 (Coronavirus disease 2019) severity, although knowledge on the response to vaccination is limited. IgG N-glycome was analyzed in this study in post-COVID-19 and post-vaccination patients to reveal potential glycosylation-based alterations using hydrophilic interaction liquid chromatography (HILIC-UPLC) with fluorescence (FLR) and mass-spectrometric (MS) detection. IgG antibodies were purified from serum samples through protein G affinity chromatography followed by PNGase F digestion-based deglycosylation. The released glycans were fluorescently derivatized by procainamide labeling and purified via solid-phase extraction. Higher levels of sialylation and afucosylation were identified in post-COVID-19 patients, which was further expanded by vaccination, but only in those who were previously SARS-CoV-2 (Severe acute respiratory syndrome coronavirus 2) infected.

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Concepts Keywords
Chromatography Adult
Coronavirus Aged
Covid Antibodies, Viral
Vaccination Antibodies, Viral
antibody glycosylation
COVID-19
COVID-19
COVID-19 Vaccines
COVID-19 Vaccines
Female
Glycoproteins
Glycoproteins
glycosylated IgG
Glycosylation
Humans
Immunoglobulin G
Immunoglobulin G
liquid chromatography
Male
Middle Aged
Polysaccharides
Polysaccharides
SARS-CoV-2
Vaccination
vaccination

Semantics

Type Source Name
disease MESH COVID-19
disease IDO protein
pathway REACTOME Digestion
drug DRUGBANK Procainamide
disease IDO blood
pathway REACTOME Immune System
disease MESH viral infections
disease IDO production
drug DRUGBANK L-Asparagine
disease MESH infection
drug DRUGBANK Coenzyme M
drug DRUGBANK Hexocyclium
drug DRUGBANK Formic Acid
drug DRUGBANK Acetic acid
drug DRUGBANK Dimethyl sulfoxide
drug DRUGBANK Water
drug DRUGBANK Flunarizine
disease MESH Allergy
disease MESH bacterial diseases
disease IDO intervention

Original Article

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