Multiplexed antigen panel analysis identifies B cell phenotype and receptor genetic contributions to antibody breadth

The cellular, immunogenetic, and antigenic factors affecting the breadth of viral antigen variants recognized by human antibody responses are poorly defined. We developed highly multiplexed panels of DNA-tagged SARS-CoV-2 antigens from up to 20 viral variants to label and sort 6,262 antigen-binding circulating B cells from previously naive mRNA vaccinees or infected patients, and from deceased organ donor lymphoid tissues, to enable antigen receptor and transcriptome sequencing. Atypical B cells and a subset of class-switched memory cells with evidence of recent germinal center exposure were enriched for antigen binding. In contrast to atypical B cells, post-germinal center B cells showed progressively increasing variant binding breadth and somatic hypermutation over time. Vaccination, compared with infection, preferentially stimulated B cells expressing antibodies with inherently high antigen-binding breadth. This large-scale analysis reveals key determinants of antigen-binding breadth, critical for understanding responses to viral infection and guiding vaccine development against rapidly mutating viruses.

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Publication Details

Journal
Immunity
Published
2026-04-01
DOI
https://doi.org/10.1016/j.immuni.2026.03.006
Citations
1
Primary Topic
T-cell and B-cell Immunology
Type
article
Field-Weighted Citation Impact
13.13

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article

Multiplexed antigen panel analysis identifies B cell phenotype and receptor genetic contributions to antibody breadth

Javaria Najeeb, Ana Rita Otrelo-Cardoso, Brandon Lam, Prasanti Kotagiri et al.
1 citations
Immunity
T-cell and B-cell Immunology
13.13
article

Multiplexed antigen panel analysis identifies B cell phenotype and receptor genetic contributions to antibody breadth

Javaria Najeeb, Ana Rita Otrelo-Cardoso, Brandon Lam, Prasanti Kotagiri, Jacob N. Wohlstadter, Emily Haraguchi, Jackson Schuetz, Donna Smith, Linda M. Liao, Bali Pulendran, Katharina Röltgen, Mark Davis, Evan Do, Prabhu S. Arunachalam, Erin Craig, Ramona A. Hoh, Stuart A. Scott, Taylor Pursell, Chandler Ho, Benjamin A. Pinsky, Scott D. Boyd, Jumana Afaghani, Sean Van Slyck, Claus U. Niemann, George B. Sigal, Oliver F. Wirz, Theodore S. Jardetzky, Jeremy Minshull, Sandra C. A. Nielsen, Andrea Fernandes, I. D. Chang, Molly Hunter, Kari C. Nadeau, Ji-Yeun Lee, Brian Ha, Fan Yang
article en
1 citations

Abstract

The cellular, immunogenetic, and antigenic factors affecting the breadth of viral antigen variants recognized by human antibody responses are poorly defined. We developed highly multiplexed panels of DNA-tagged SARS-CoV-2 antigens from up to 20 viral variants to label and sort 6,262 antigen-binding circulating B cells from previously naive mRNA vaccinees or infected patients, and from deceased organ donor lymphoid tissues, to enable antigen receptor and transcriptome sequencing. Atypical B cells and a subset of class-switched memory cells with evidence of recent germinal center exposure were enriched for antigen binding. In contrast to atypical B cells, post-germinal center B cells showed progressively increasing variant binding breadth and somatic hypermutation over time. Vaccination, compared with infection, preferentially stimulated B cells expressing antibodies with inherently high antigen-binding breadth. This large-scale analysis reveals key determinants of antigen-binding breadth, critical for understanding responses to viral infection and guiding vaccine development against rapidly mutating viruses.

Immunity
Swiss Tropical and Public Health Institute (CH), University of California, San Francisco (US), University of Basel (CH), Beth Israel Deaconess Hospital (US), Stanford Health Care (US), ATUM (United States) (US), Stanford Medicine (US), Shenzhen Institutes of Advanced Technology (CN), Sierra Engineering (United States) (US), Meso Scale Discovery (United States) (US), Monash University (AU), Stanford University (US)
Meso Scale Diagnostics, National Institutes of Health
Zero hunger
Openalex Percentile: Top 1%
T-cell and B-cell Immunology
13.13
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