XBB.1.5 monovalent booster improves antibody binding and neutralization against emerging SARS-CoV-2 Omicron variants.

Shilpi Jain,Sanjeev Kumar,Lilin Lai,Susanne Linderman, Ansa A Malik,Madison L Ellis,Sucheta Godbole,Daniel Solis,Malaya K Sahoo, Kareem Bechnak, Isabel Paredes, Ralph Tanios,Bahaa Kazzi, Serena M Dib, Matthew B Litvack, Sonia T Wimalasena, Caroline Ciric,Christina Rostad, Richard West,I-Ting Teng, Danyi Wang, Sri Edupuganti,Peter D Kwong,Nadine Rouphael,Benjamin A Pinsky,Daniel C Douek,Jens Wrammert,Alberto Moreno,Mehul S Suthar

bioRxiv : the preprint server for biology(2024)

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摘要
The rapid emergence of divergent SARS-CoV-2 variants has led to an update of the COVID-19 booster vaccine to a monovalent version containing the XBB.1.5 spike. To determine the neutralization breadth following booster immunization, we collected blood samples from 24 individuals pre- and post-XBB.1.5 mRNA booster vaccination (∼1 month). The XBB.1.5 booster improved both neutralizing activity against the ancestral SARS-CoV-2 strain (WA1) and the circulating Omicron variants, including EG.5.1, HK.3, HV.1, XBB.1.5 and JN.1. Relative to the pre-boost titers, the XBB.1.5 monovalent booster induced greater total IgG and IgG subclass binding, particular IgG4, to the XBB.1.5 spike as compared to the WA1 spike. We evaluated antigen-specific memory B cells (MBCs) using either spike or receptor binding domain (RBD) probes and found that the monovalent booster largely increases non-RBD cross-reactive MBCs. These data suggest that the XBB.1.5 monovalent booster induces cross-reactive antibodies that neutralize XBB.1.5 and related Omicron variants.
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