iScience (Apr 2025)

BA.1 breakthrough infection elicits distinct antibody and memory B cell responses in vaccinated-only versus hybrid immunity individuals

  • Carla Saade,
  • Timothée Bruel,
  • Lou-Léna Vrignaud,
  • Martin Killian,
  • Annabelle Drouillard,
  • Véronique Barateau,
  • Maxime Espi,
  • Natacha Mariano,
  • Charlotte Mignon,
  • Lily Bruyère,
  • Liliane Khoryati,
  • William Henry Bolland,
  • Olivier Schwartz,
  • Bruno Lina,
  • Martine Valette,
  • Olivier Thaunat,
  • Jean-Baptiste Fassier,
  • Bruno Pozzetto,
  • Stéphane Paul,
  • Thierry Walzer,
  • Sophie Trouillet-Assant,
  • Nicolas Guibert,
  • Gregory Destras,
  • Dulce Alfaiate,
  • Amélie Massardier-Pilonchery,
  • Antonin Bal,
  • Hélène Lozano,
  • Bouchra Mokdad,
  • Kahina Saker,
  • Cécile Barnel,
  • Caroline Dupré,
  • Fanny Joubert,
  • Camille Mena,
  • Virginie Pitiot,
  • Vanessa Escuret,
  • Florence Morfin,
  • Mary-Anne Trabaud,
  • Laurence Josset,
  • Antonin Bal

DOI
https://doi.org/10.1016/j.isci.2025.111962
Journal volume & issue
Vol. 28, no. 4
p. 111962

Abstract

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Summary: Immune memory is influenced by the frequency and type of antigenic challenges. Here, we performed a cross-sectional comparison of immune parameters following a BA.1 breakthrough infection in individuals with prior hybrid immunity (conferred by infection and vaccination) versus those solely vaccinated in a cohort of health care workers in Lyon, France. The results showed higher levels of serum anti-receptor binding domain (RBD) antibodies and neutralizing antibodies against BA.1 post-infection in the vaccine-only group. Individuals in this group also showed a decrease in memory B cells against the ancestral strain but an increase in those specific and cross-reactive to BA.1, suggesting a more limited immune imprinting. Conversely, hybrid immunity prevents the decrease in antibody dependent cellular cytotoxicity (ADCC) response, possibly by limiting IgG4 class-switching and enhanced anti-N responses post-infection. This highlights that BA.1 breakthrough infection induces different immune responses depending on prior history of vaccination and infection, which should be considered for further vaccination guidelines.

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