XBB.1.5 monovalent booster improves antibody binding and neutralization against emerging SARS-CoV-2 Omicron variants
Shilpi JainiD, Sanjeev KumariD, Lilin LaiiD, Susanne L. LindermaniD, Ansa A. Malik, Madison Leigh EllisiD, Sucheta GodboleiD, Daniel SolisiD, Malaya Kumar SahooiD, Kareem BechnakiD, Isabel ParedesiD, Ralph Tanios, Bahaa KazziiD, Serena M. Dib, Matthew B. Litvack, Sonia Tandon WimalasenaiD, Caroline Rose Ciric, Christina A. RostadiD, Richard West, I‐Ting TengiD, Danyi WangiD, Sri Edupuganti, Peter D. KwongiD, Nadine RouphaeliD, Benjamin A. PinskyiD, , Mehul S. SuthariD
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.
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