Author Identifier (ORCID)

wei wang

https://orcid.org/0000-0002-1430-1360

Abstract

Coronavirus disease 2019 (COVID-19) remains a major health challenge globally. Previous studies have suggested that changes in the glycosylation of IgG are closely associated with the severity of COVID-19. This study aimed to compare the profiles of IgG N-glycome between COVID-19 patients and healthy controls. A case-control study was conducted, in which 104 COVID-19 patients and 104 age- and sex-matched healthy individuals were recruited. Serum IgG N-glycome composition was analyzed by hydrophilic interaction liquid chromatography with the ultra-high-performance liquid chromatography (HILIC-UPLC) approach. COVID-19 patients have a decreased level of IgG fucosylation, which upregulates antibody-dependent cell cytotoxicity (ADCC) in acute immune responses. In severe cases, a low level of IgG sialylation contributes to the ADCC-regulated enhancement of inflammatory cytokines. The decreases in sialylation and galactosylation play a role in COVID-19 pathogenesis via the activation of the lectin-initiated alternative complement pathway. IgG N-glycosylation underlines the complex clinical phenotypes of SARS-CoV-2 infection.

Document Type

Journal Article

Date of Publication

2021

Publication Title

Frontiers in Immunology

Publisher

Frontiers Media S.A.

School

School of Medical and Health Sciences

RAS ID

37014

Funders

Edith Cowan University - Open Access Support Scheme 2021

National Health and Medical Research Council

National Natural Science Foundation of China

China-Australia International Collaborative Grant

European Commission Horizon 2020 Framework Program

Grant Number

NHMRC Number : APP1112767

Creative Commons License

Creative Commons Attribution 4.0 License
This work is licensed under a Creative Commons Attribution 4.0 License.

Comments

Hou, H., Yang, H., Liu, P., Huang, C., Wang, M., Li, Y., . . . Wang, W. (2021). Profile of immunoglobulin G N-glycome in COVID-19 patients: A case-control study. Frontiers in Immunology, 12, article 748566. https://doi.org/10.3389/fimmu.2021.748566

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Link to publisher version (DOI)

10.3389/fimmu.2021.748566