4.8 Article

MAIT cells contribute to protection against lethal influenza infection in vivo

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NATURE COMMUNICATIONS
卷 9, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-018-07207-9

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资金

  1. Royal Society [IE160540]
  2. People Programme (Marie Curie Actions) of the European Union's Seventh Framework Programme (FP7/2007-2013) under REA grant [608765]
  3. National Health and Medical Research Council of Australia (NHMRC) Program [1113293, 1071916, 1016629, 606788, 1120467]
  4. ARC
  5. ARC DECRA Fellowship
  6. Melbourne International Engagement Award (University of Melbourne)
  7. Melbourne International Research Scholarship
  8. Melbourne International Fee Remission Scholarship (University of Melbourne)
  9. Victoria India Doctoral Scholarship, University of Melbourne
  10. Melbourne International Fee Remission Scholarship, University of Melbourne
  11. Melbourne International Fee Remission Scholarships
  12. NHMRC Senior Principal Research Fellowship [1117766]
  13. Australian Research Council (ARC) [CE140100011]
  14. NIHR Senior Fellowship
  15. Oxford Martin School
  16. Wellcome Trust [WT109965MA, 104553/z/14/z]
  17. Sylvia and Charles Viertel fellowship
  18. National Health and Medical Research Council of Australia [1120467] Funding Source: NHMRC

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Mucosal associated invariant T (MAIT) cells are evolutionarily-conserved, innate-like lymphocytes which are abundant in human lungs and can contribute to protection against pulmonary bacterial infection. MAIT cells are also activated during human viral infections, yet it remains unknown whether MAIT cells play a significant protective or even detrimental role during viral infections in vivo. Using murine experimental challenge with two strains of influenza A virus, we show that MAIT cells accumulate and are activated early in infection, with upregulation of CD25, CD69 and Granzyme B, peaking at 5 days post-infection. Activation is modulated via cytokines independently of MR1. MAIT cell-deficient MR1(-/-)mice show enhanced weight loss and mortality to severe (H1N1) influenza. This is ameliorated by prior adoptive transfer of pulmonary MAIT cells in both immunocompetent and immunodeficient RAG2(-/-)gamma C-/- mice. Thus, MAIT cells contribute to protection during respiratory viral infections, and constitute a potential target for therapeutic manipulation.

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