bioRxiv · 10.1101/2021.09.09.459504
Differential antibody dynamics to SARS-CoV-2 infection and vaccination
Abstract
Optimal immune responses furnish long-lasting (durable) antibodies protective across dynamically mutating viral variants (broad). To assess robustness of mRNA vaccine-induced immunity, we compared antibody durability and breadth after SARS-CoV-2 infection and vaccination. While vaccination delivered robust initial virus-specific antibodies with some cross-variant coverage, pre-variant SARS-CoV-2 infection-induced antibodies, while modest in magnitude, showed highly stable long-term antibody dynamics. Vaccination after infection induced maximal antibody magnitudes with enhanced longitudinal stability while infection-naive vaccinee antibodies fell with time to post-infection-alone levels. The composition of antibody neutralizing activity to variant relative to original virus also differed between groups, with infection-induced antibodies demonstrating greater relative breadth. Differential antibody durability trajectories favored COVID-19-recovered subjects with dual memory B cell features of greater early antibody somatic mutation and cross-coronavirus reactivity. By illuminating an infection-mediated antibody breadth advantage and an anti-SARS-CoV-2 antibody durability-enhancing function conferred by recalled immunity, these findings may serve as guides for ongoing vaccine strategy improvement.
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Chen, Y., Tong, P., Whiteman, N. B., Moghaddam, A. S., Zuiani, A., Habibi, S., Gautam, A., Xiao, T., Cai, Y., Chen, B., Wesemann, D. R.. 2021-09-10. Differential antibody dynamics to SARS-CoV-2 infection and vaccination. https://doi.org/10.1101/2021.09.09.459504
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