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10.3389/fimmu.2021.748566

http://scihub22266oqcxt.onion/10.3389/fimmu.2021.748566
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suck abstract from ncbi


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pmid34630427      Front+Immunol 2021 ; 12 (ä): 748566
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  • Profile of Immunoglobulin G N-Glycome in COVID-19 Patients: A Case-Control Study #MMPMID34630427
  • Hou H; Yang H; Liu P; Huang C; Wang M; Li Y; Zhu M; Wang J; Xu Y; Wang Y; Ma Q; Li D; Liao P; Wang W
  • Front Immunol 2021[]; 12 (ä): 748566 PMID34630427show ga
  • 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.
  • |Adult[MESH]
  • |Antibody-Dependent Cell Cytotoxicity[MESH]
  • |COVID-19/*metabolism[MESH]
  • |Case-Control Studies[MESH]
  • |Chromatography, High Pressure Liquid[MESH]
  • |Complement Pathway, Mannose-Binding Lectin[MESH]
  • |Female[MESH]
  • |Glycosylation[MESH]
  • |Humans[MESH]
  • |Immunoglobulin G/*metabolism[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Phenotype[MESH]


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