Multi-compartmental diversification of neutralizing antibody lineages dissected in SARS-CoV-2 spike-immunized macaques.
Mandolesi, M., Das, H., de Vries, L., Yang, Y., Kim, C., Dhinakaran, M., Castro Dopico, X., Fischbach, J., Kim, S., Guryleva, M.V., Adori, M., Chernyshev, M., Stalmarck, A., Hanke, L., McInerney, G.M., Sheward, D.J., Corcoran, M., Hallberg, B.M., Murrell, B., Karlsson Hedestam, G.B.(2024) Nat Commun 15: 6338-6338
- PubMed: 39068149
- DOI: https://doi.org/10.1038/s41467-024-50286-0
- Primary Citation of Related Structures:
8P5M, 8Q5Y - PubMed Abstract:
The continued evolution of SARS-CoV-2 underscores the need to understand qualitative aspects of the humoral immune response elicited by spike immunization. Here, we combine monoclonal antibody (mAb) isolation with deep B cell receptor (BCR) repertoire sequencing of rhesus macaques immunized with prefusion-stabilized spike glycoprotein. Longitudinal tracing of spike-sorted B cell lineages in multiple immune compartments demonstrates increasing somatic hypermutation and broad dissemination of vaccine-elicited B cells in draining and non-draining lymphoid compartments, including the bone marrow, spleen and, most notably, periaortic lymph nodes. Phylogenetic analysis of spike-specific monoclonal antibody lineages identified through deep repertoire sequencing delineates extensive intra-clonal diversification that shaped neutralizing activity. Structural analysis of the spike in complex with a broadly neutralizing mAb provides a molecular basis for the observed differences in neutralization breadth between clonally related antibodies. Our findings highlight that immunization leads to extensive intra-clonal B cell evolution where members of the same lineage can both retain the original epitope specificity and evolve to recognize additional spike variants not previously encountered.
Organizational Affiliation:
Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden. marco.mandolesi.job@gmail.com.