4.7 Article

Human CD8+ T cell cross-reactivity across influenza A, B and C viruses

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NATURE IMMUNOLOGY
卷 20, 期 5, 页码 613-+

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NATURE PUBLISHING GROUP
DOI: 10.1038/s41590-019-0320-6

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资金

  1. Australian National Health and Medical Research Council (NHMRC) NHMRC Program Grant [1071916]
  2. Melbourne International research scholarship
  3. Victoria India doctoral scholarship
  4. ARC laureate fellowship
  5. Australian Government Department of Health
  6. NHMRC principal research fellowship [1137739]
  7. NHMRC project grant [1085018]
  8. US National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health, Department of Health and Human Services [HHSN272201400006C]
  9. NHMRC Peter Doherty fellowship [1072159]
  10. St. Jude Center of Excellence for Influenza Research and Surveillance (NIAID) [HHSN27220140006C]
  11. American Lebanese Syrian Associated Charities
  12. JDRF Career Development award [5-CDA2014210-A-N]
  13. NHMRC Project [GNT 1123586]
  14. Melbourne International fee remission scholarship
  15. Melbourne International fee remission scholarship, University of Melbourne
  16. [R01AI107625]
  17. [R01AI136514]
  18. National Health and Medical Research Council of Australia [1072159, 1085018] Funding Source: NHMRC

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Influenza A, B and C viruses (IAV, IBV and ICV, respectively) circulate globally and infect humans, with IAV and IBV causing the most severe disease. CD8(+) T cells confer cross-protection against IAV strains, however the responses of CD8(+) T cells to IBV and ICV are understudied. We investigated the breadth of CD8(+) T cell cross-recognition and provide evidence of CD8(+) T cell cross-reactivity across IAV, IBV and ICV. We identified immunodominant CD8(+) T cell epitopes from IBVs that were protective in mice and found memory CD8(+) T cells directed against universal and influenza-virus-type-specific epitopes in the blood and lungs of healthy humans. Lung-derived CD8(+) T cells displayed tissue-resident memory phenotypes. Notably, CD38(+)Ki67(+)CD8(+) effector T cells directed against novel epitopes were readily detected in IAV- or IBV-infected pediatric and adult subjects. Our study introduces a new paradigm whereby CD8(+) T cells confer unprecedented cross-reactivity across all influenza viruses, a key finding for the design of universal vaccines.

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