Journal
SCIENCE IMMUNOLOGY
Volume 7, Issue 67, Pages -Publisher
AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/sciimmunol.abk3070
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Funding
- Mark and Lisa Schwartz Foundation
- Massachusetts Consortium for Pathogen Readiness
- Ragon Institute of MGH, MIT, and Harvard
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HLA genotype conditions the CD8(+) T cell response to SARS-CoV-2, influencing epitope specificity, TCR sequence diversity, and utilization of immune memory T cells. Single-cell transcriptomics revealed functional diversity of SARS-CoV-2-reactive T cells associated with disease stage and epitope specificity.
Effective presentation of antigens by human leukocyte antigen (HLA) class I molecules to CD8(+) T cells is required for viral elimination and generation of long-term immunological memory. In this study, we applied a single-cell, multiomic technology to generate a unified ex vivo characterization of the CD8(+) T cell response to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) across four major HLA class I alleles. We found that HLA genotype conditions key features of epitope specificity, TCR alpha/beta sequence diversity, and the utilization of pre-existing SARS-CoV-2-reactive memory T cell pools. Single-cell transcriptomics revealed functionally diverse T cell phenotypes of SARS-CoV-2-reactive T cells, associated with both disease stage and epitope specificity. Our results show that HLA variations notably influence the CD8(+) T cell repertoire shape and utilization of immune recall upon SARS-CoV-2 infection.
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