Genetic markers of enhanced functional antibody responses to COVID-19 vaccination
Journal Title
Vaccine
Publication Type
Research article
Abstract
INTRODUCTION: Substantial population-level variation in vaccine-specific antibody responses has been observed following global coronavirus disease 2019 (COVID-19) vaccination efforts. Beyond the influence of clinical and demographic features, immunogenetic variation is suggested to underlie divergent serological responses following COVID-19 vaccination of distinct populations. METHODS: Immunoglobulin G1 (IgG1) allotypic markers (G1m) for 121 COVID-19 vaccinated healthy adults were genotyped via Sanger sequencing. Vaccine-specific IgG and Fc gamma receptor (FcγR) engagement were characterised via bead-based multiplex array. RESULTS: Following two COVID-19 vaccine doses, G1m1,17(+/+) compared to G1m-1,3(+/+) vaccinees had increased IgG and FcγR engagement specific for the antigenically conserved SARS-CoV-2 Spike 2 (S2) domain. IgG targeting antigenically novel SARS-CoV-2 receptor binding domain (RBD) trended higher in G1m1,17(+/+) vaccinees, facilitating increased RBD-specific FcγR2a-R131 and FcγR2b binding. CONCLUSION: Primary COVID-19 vaccination induced increased S2-specific IgG in G1m1,17(+/+) vaccinees, facilitating enhanced anti-viral FcγR engagement and suggesting immunogenetics may be a valuble consideration for next-generation vaccine design.
Keywords
Fc functions; FcγR polymorphism; IgG Allotype; Immunogenetics; SARS-CoV-2; Vaccine
Department(s)
Infectious Diseases
Open Access at Publisher's Site
https://doi.org/10.1016/j.vaccine.2025.127379
Terms of Use/Rights Notice
Refer to copyright notice on published article.


Creation Date: 2025-08-08 07:40:11
Last Modified: 2025-08-08 07:42:02
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