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

Journal: BioRxiv : The Preprint Server For Biology
Published:
Abstract

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.

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