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J Med Virol . Neutralization of SARS-CoV-2 Omicron XBB.1.5 and JN.1 variants after COVID-19 booster-vaccination and infection

tetano

Editor, Senior Moderator
J Med Virol


. 2024 Jul;96(7):e29801.
doi: 10.1002/jmv.29801. Neutralization of SARS-CoV-2 Omicron XBB.1.5 and JN.1 variants after COVID-19 booster-vaccination and infection

David N Springer[SUP] 1 [/SUP], Jeremy V Camp[SUP] 1 [/SUP], Stephan W Aberle[SUP] 1 [/SUP], Josef Deutsch[SUP] 2 [/SUP], Oliver Lammel[SUP] 3 [/SUP], Lukas Weseslindtner[SUP] 1 [/SUP], Karin Stiasny[SUP] 1 [/SUP], Judith H Aberle[SUP] 1 [/SUP]



Affiliations
Abstract

SARS-CoV-2 Omicron lineages continue to emerge and evolve into new sublineages, causing infection waves throughout 2022 and 2023, which has been attributed to immune escape. We examined neutralizing antibody responses to the recently emerged SARS-CoV-2 JN.1 variant in comparison to ancestral D614G and Omicron BA.1, BA.2, BA.5, and XBB.1.5 variants. We tested 79 human sera from cohorts with different combinations of vaccinations and infections, including 23 individuals who had been repeatedly exposed to Omicron. Individuals with a monovalent XBB.1.5 vaccine booster or XBB.1.5 breakthrough infection had robust antibody levels against all variants tested; however, JN.1 evaded antibodies in individuals after single Omicron BA.1, BA.2 or BA.5 breakthrough infections. Moreover, in the non-vaccinated cohort, serum antibodies demonstrated almost no cross-neutralization activities against D614G, XBB.1.5 and JN.1. after infections with earlier Omicron variants. These findings show that SARS-CoV-2-immunity is heterogeneous, depending on different combinations of vaccinations and infections, and emphasize the importance of considering different immune-backgrounds when evaluating novel variants.

Keywords: JN.1; Omicron 2.86; Omicron breakthrough infection; XBB; neutralizing antibodies.

 
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