Litcius/Paper detail

Structure of a Vaccine-Induced, Germline-Encoded Human Antibody Defines a Neutralizing Epitope on the SARS-CoV-2 Spike N-Terminal Domain

Clara G. Altomare, Daniel C. Adelsberg, Juan Manuel Carreño, Iden A. Sapse, Fatima Amanat, Ali H. Ellebedy, Viviana Simon, Florian Krammer, Goran Bajic

2022mBio28 citationsDOIOpen Access PDF

Abstract

We report the first structure of a vaccine-induced antibody to SARS-CoV-2 spike isolated from plasmablasts 7 days after vaccination. The genetic sequence of the antibody PVI.V6-14 suggests that it is completely unmutated, meaning that this type of B cell did not undergo somatic hypermutation or affinity maturation; this cell was likely already present in the donor and was activated by the vaccine. This is, to our knowledge, also the first structure of an unmutated antibody in complex with its cognate antigen. PVI.V6-14 binds a novel, conserved epitope on the N-terminal domain (NTD) and neutralizes the original viral strain. PVI.V6-14 also binds the newly emerged variants B.1.1.7 (alpha), B.1.351 (beta), B.1.617.2 (delta), and B.1.1.529 (omicron). Given that this antibody was likely already present in the donor prior to vaccination, we believe that this antibody class could potentially "keep up" with the new variants, should they continue to emerge, by undergoing somatic hypermutation and affinity maturation.

Topics & Concepts

Somatic hypermutationVirologyAntibodyGermlineEpitopeBiologySpike ProteinSpike (software development)VaccinationGeneticsB cellGeneCoronavirus disease 2019 (COVID-19)MedicineDiseaseEconomicsManagementInfectious disease (medical specialty)PathologySARS-CoV-2 and COVID-19 ResearchAnimal Virus Infections StudiesViral gastroenteritis research and epidemiology