# COVID-19 and blood group-related antigens: can natural anti-carbohydrate antibodies provide innate protection from symptomatic SARS-CoV-2 infection?

**Authors:** Tasnuva Ahmed, Adrien Breiman, Marjahan Akhtar, Golap Babu, Nasrin Pervin, Md Golam Firoj, Afroza Akter, Firdausi Qadri, Fahima Chowdhury, Taufiqur Rahman Bhuiyan, Jacques Le Pendu, Nathalie Ruvoën-Clouet

PMC · DOI: 10.3389/fmed.2025.1554785 · Frontiers in Medicine · 2025-04-30

## TL;DR

This study explores whether natural antibodies related to blood groups can protect against symptomatic SARS-CoV-2 infection and influence disease severity.

## Contribution

The study investigates the role of natural anti-carbohydrate antibodies in innate protection against symptomatic SARS-CoV-2 infection.

## Key findings

- Symptomatic patients had lower anti-A antibody titers compared to healthy controls.
- Anti-A and anti-B antibodies in asymptomatic patients showed higher trends up to three months post-infection.
- Gender and blood group differences suggest innate immune factors may influence disease severity.

## Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) primarily targets respiratory mucosa, causing coronavirus disease 2019 (COVID-19). Susceptibility and severity of COVID-19 may be influenced by predisposing factors including blood groups. In this study, we investigated whether natural anti-carbohydrate antibodies provide innate protection against SARS-CoV-2 and influence disease severity.

We used samples (plasma and saliva) from a longitudinal cohort study in Bangladesh that enrolled 100 COVID-19 symptomatic and asymptomatic patients. We also enrolled 21 and 38 healthy controls during the pandemic period and pre-pandemic period, respectively. We phenotype ABO blood grouping from blood and determined Lewis and secretor status (H antigen) from the saliva samples. We quantified natural anti-carbohydrate antibodies (anti-A, anti-B, anti-Tn-Mono and anti-αGal IgG, IgA, and IgM) from plasma collected at enrollment. We also explored the trend of natural anti-carbohydrate antibodies until 3 months of convalescence period among the COVID-19 patients (day 14 and day 90 from enrollment). Antibody quantification and ABH/Lewis phenotyping were performed using enzyme-linked immunosorbent assay (ELISA).

We included 99 COVID-19 patients and 59 healthy controls assessing the differences of natural antibody titer during enrollment, while 95 patients were analyzed exploring Lewis and secretor status with natural antibody titer and disease status. We did not find significant difference in the distribution for neither ABO blood groups nor non-secretors and Lewis-negative individuals among asymptomatic or symptomatic patients and healthy controls. Nonetheless, we observed lower anti-A antibody titers among symptomatic patients compared to healthy controls. We also identified slight differences in antibody titers linked to age and gender. Anti-A and anti-B antibodies among asymptomatic patients had a higher trend up to 3 months from infection compared to symptomatic patients.

Higher natural anti-A and anti-B antibody titers may offer protection against symptomatic COVID-19 infections. Gender and blood group differences indicate potential innate immune factors influencing disease severity, but larger studies are needed to confirm these findings.

## Linked entities

- **Diseases:** coronavirus disease 2019 (MONDO:0100096)

## Full-text entities

- **Genes:** ACE2 (angiotensin converting enzyme 2) [NCBI Gene 59272] {aka ACEH}, HBG1 (hemoglobin subunit gamma 1) [NCBI Gene 3047] {aka HBG-T2, HBGA, HBGR, HSGGL1, PRO2979}, MBOAT4 (membrane bound ghrelin O-acyltransferase MBOAT4) [NCBI Gene 619373] {aka FKSG89, GOAT, OACT4}, FUT4 (fucosyltransferase 4) [NCBI Gene 2526] {aka CD15, ELFT, FCT3A, FUC-TIV, FUTIV, LeX}, FUT2 (fucosyltransferase 2 (H blood group)) [NCBI Gene 2524] {aka B12QTL1, SE, SEC2, Se2, sej}, ALKBH1 (alkB homolog 1, histone H2A dioxygenase) [NCBI Gene 8846] {aka ABH, ABH1, ALKBH, alkB, hABH}, GAL (galanin and GMAP prepropeptide) [NCBI Gene 51083] {aka ETL8, GAL-GMAP, GALN, GLNN, GMAP}, FUT3 (fucosyltransferase 3 (Lewis blood group)) [NCBI Gene 2525] {aka CD174, FT3B, FucT-III, LE, Les}, CD79A (CD79a molecule) [NCBI Gene 973] {aka IGA, IGAlpha, MB-1, MB1}, ABO (ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase) [NCBI Gene 28] {aka A3GALNT, A3GALT1, GTA, GTB, NAGAT}, MUC5AC (mucin 5AC, oligomeric mucus/gel-forming) [NCBI Gene 4586] {aka MUC5, TBM, leB, mucin}, CLEC3B (C-type lectin domain family 3 member B) [NCBI Gene 7123] {aka MCDR4, TN, TNA}
- **Diseases:** viral diseases (MESH:D014777), gastroenteritis (MESH:D005759), infectious diseases (MESH:D003141), infected (MESH:D007239), rotavirus infection (MESH:D012400), Diarrhoeal Disease (MESH:D004194), COVID-19 (MESH:D000086382)
- **Chemicals:** carbohydrate (MESH:D002241), oxygen (MESH:D010100), trisaccharide (MESH:D014312), monosaccharide (MESH:D009005), phosphoric acid (MESH:C030242), T (MESH:D014316), GalNAcalpha1,3-(Fucalpha1,2)-Galss-PAA (-), saline (MESH:D012965), phosphate (MESH:D010710), 3,3',5,5'-tetramethylbenzidine (MESH:C021758), bicarbonate (MESH:D001639), alpha-gal (MESH:C055075), glycan (MESH:D011134), A-Tri (MESH:C069225), oligosaccharides (MESH:D009844), Tween 20 (MESH:D011136), carbonate (MESH:D002254), PBS (MESH:D007854), sugar (MESH:D000073893), phosphorous acid (MESH:C570063)
- **Species:** Rotavirus (genus) [taxon 10912], Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Severe acute respiratory syndrome-related coronavirus (no rank) [taxon 694009]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12074924/full.md

## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC12074924/full.md

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Source: https://tomesphere.com/paper/PMC12074924