| Literature DB >> 33643275 |
Adrien Breiman1,2, Nathalie Ruvoën-Clouet1,3, Marie Deleers4,5, Tiffany Beauvais1,2, Nicolas Jouand6, Jézabel Rocher1, Nicolai Bovin7, Nathalie Labarrière1, Hanane El Kenz4,5, Jacques Le Pendu1.
Abstract
Human serum contains large amounts of anti-carbohydrate antibodies, some of which may recognize epitopes on viral glycans. Here, we tested the hypothesis that such antibodies may confer protection against COVID-19 so that patients would be preferentially found among people with low amounts of specific anti-carbohydrate antibodies since individual repertoires vary considerably. After selecting glycan epitopes commonly represented in the human anti-carbohydrate antibody repertoire that may also be expressed on viral glycans, plasma levels of the corresponding antibodies were determined by ELISA in 88 SARS-CoV-2 infected individuals, including 13 asymptomatic, and in 82 non-infected controls. We observed that anti-Tn antibodies levels were significantly lower in patients as compared to non-infected individuals. This was not observed for any of the other tested carbohydrate epitopes, including anti-αGal antibodies used as a negative control since the epitope cannot be synthesized by humans. Owing to structural homologies with blood groups A and B antigens, we also observed that anti-Tn and anti-αGal antibodies levels were lower in blood group A and B, respectively. Analyses of correlations between anti-Tn and the other anti-carbohydrates tested revealed divergent patterns of correlations between patients and controls, suggesting qualitative differences in addition to the quantitative difference. Furthermore, anti-Tn levels correlated with anti-S protein levels in the patients' group, suggesting that anti-Tn might contribute to the development of the specific antiviral response. Overall, this first analysis allows to hypothesize that natural anti-Tn antibodies might be protective against COVID-19.Entities:
Keywords: COVID-19; O-glycans; Tn antigen; histo-blood group antigens; natural antibodies
Year: 2021 PMID: 33643275 PMCID: PMC7905038 DOI: 10.3389/fmicb.2021.641460
Source DB: PubMed Journal: Front Microbiol ISSN: 1664-302X Impact factor: 5.640