open access publication

Article, 2024

Simultaneous analysis of pMHC binding and reactivity unveils virus-specific CD8 T cell immunity to a concise epitope set

SCIENCE ADVANCES, ISSN 2375-2548, 2375-2548, Volume 10, 15, 10.1126/sciadv.adm8951

Contributors

Kristensen, Nikolaj Pagh 0000-0002-5073-7153 [1] Dionisio, E. [1] Bentzen, A. K. 0000-0002-5184-3054 [1] [2] [3] Tamhane, Tripti [1] Kemming, J. S. [1] Nos, Grigorii 0000-0002-8066-7424 [1] Voss, Lasse Frank 0000-0003-0904-6753 [1] Hansen, Ulla 0000-0001-9668-8038 [1] Lauer, Georg 0000-0002-9792-4271 [4] [5] [6] Hadrup, S. R. 0000-0002-5937-4344 (Corresponding author) [1]

Affiliations

  1. [1] Tech Univ Denmark DTU, Dept Hlth Technol, Sect Expt & Translat Immunol, Lyngby, Denmark
  2. [NORA names: DTU Technical University of Denmark; University; Denmark; Europe, EU; Nordic; OECD];
  3. [2] UCL Canc Inst, London, England
  4. [NORA names: United Kingdom; Europe, Non-EU; OECD];
  5. [3] UCL Canc Inst, London, England
  6. [NORA names: United Kingdom; Europe, Non-EU; OECD];
  7. [4] Harvard Med Sch, Boston, MA 02114 USA
  8. [NORA names: United States; America, North; OECD];
  9. [5] Harvard Med Sch, Boston, MA 02114 USA
  10. [NORA names: United States; America, North; OECD];

Abstract

CD8 T cells provide immunity to virus infection through recognition of epitopes presented by peptide major histocompatibility complexes (pMHCs). To establish a concise panel of widely recognized T cell epitopes from common viruses, we combined analysis of TCR down-regulation upon stimulation with epitope-specific enumeration based on barcode-labeled pMHC multimers. We assess CD8 T cell binding and reactivity for 929 previously reported epitopes in the context of 1 of 25 HLA alleles representing 29 viruses. The prevalence and magnitude of CD8 T cell responses were evaluated in 48 donors and reported along with 137 frequently recognized virus epitopes, many of which were underrepresented in the public domain. Eighty-four percent of epitope-specific CD8 T cell populations demonstrated reactivity to peptide stimulation, which was associated with effector and long-term memory phenotypes. Conversely, nonreactive T cell populations were associated primarily with naive phenotypes. Our analysis provides a reference map of epitopes for characterizing CD8 T cell responses toward common human virus infections.

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