Profiling antibody epitopes induced by mRNA-1273 vaccination and boosters

Front Immunol. 2024 Mar 18:15:1285278. doi: 10.3389/fimmu.2024.1285278. eCollection 2024.

Abstract

Background: Characterizing the antibody epitope profiles of messenger RNA (mRNA)-based vaccines against SARS-CoV-2 can aid in elucidating the mechanisms underlying the antibody-mediated immune responses elicited by these vaccines.

Methods: This study investigated the distinct antibody epitopes toward the SARS-CoV-2 spike (S) protein targeted after a two-dose primary series of mRNA-1273 followed by a booster dose of mRNA-1273 or a variant-updated vaccine among serum samples from clinical trial adult participants.

Results: Multiple S-specific epitopes were targeted after primary vaccination; while signal decreased over time, a booster dose after >6 months largely revived waning antibody signals. Epitope identity also changed after booster vaccination in some subjects, with four new S-specific epitopes detected with stronger signals after boosting than with primary vaccination. Notably, the strength of antibody responses after booster vaccination differed by the exact vaccine formulation, with variant-updated mRNA-1273.211 and mRNA-1273.617.2 booster formulations inducing significantly stronger S-specific signals than a mRNA-1273 booster.

Conclusion: Overall, these results identify key S-specific epitopes targeted by antibodies induced by mRNA-1273 primary and variant-updated booster vaccination.

Keywords: COVID-19; SARS-CoV-2; antibody profile; dosing regimen; mRNA-1273.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 2019-nCoV Vaccine mRNA-1273*
  • Adult
  • Antibodies
  • COVID-19 Vaccines*
  • Epitopes
  • Humans
  • RNA, Messenger / genetics
  • SARS-CoV-2
  • Vaccination
  • mRNA Vaccines

Substances

  • 2019-nCoV Vaccine mRNA-1273
  • COVID-19 Vaccines
  • Antibodies
  • Epitopes
  • RNA, Messenger
  • mRNA Vaccines

Grants and funding

The author(s) declare that financial support was received for the research, authorship, and/or publication of this article.