4.8 Article

MAIT cells are activated during human viral infections

Journal

NATURE COMMUNICATIONS
Volume 7, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/ncomms11653

Keywords

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Funding

  1. NIHR Biomedical Research Program (Oxford)
  2. Wellcome Trust [WT091663MA]
  3. National Institutes for Health Research Biomedical Research Centre (Imperial College)
  4. NIH [U19AI082630]
  5. Oxford Martin School
  6. Wellcome Trust programme Grant [PS2186_WMII]
  7. Medical Research Council
  8. MRC programme Grant [MR/K000241/1]
  9. MRC Project [G0600371]
  10. MRC intermediate fellowship programme
  11. MRC [G0600371, MC_UU_12014/9, G1100247, MC_PC_12020, MR/K01532X/1, G0400720, G1002552, MR/K000241/1, MR/K010239/1, G0801508] Funding Source: UKRI
  12. Medical Research Council [MC_PC_12020, MR/K000241/1, G1002552, MR/K010239/1, G0801508, G0400720, MR/K01532X/1, G0600000, G0600371] Funding Source: researchfish
  13. National Institute for Health Research [NF-SI-0515-10005] Funding Source: researchfish
  14. Wellcome Trust [109965/Z/15/Z] Funding Source: researchfish

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Mucosal-associated invariant T (MAIT) cells are abundant in humans and recognize bacterial ligands. Here, we demonstrate that MAIT cells are also activated during human viral infections in vivo. MAIT cells activation was observed during infection with dengue virus, hepatitis C virus and influenza virus. This activation-driving cytokine release and Granzyme B upregulation-is TCR-independent but dependent on IL-18 in synergy with IL-12, IL-15 and/or interferon-alpha/beta. IL-18 levels and MAIT cell activation correlate with disease severity in acute dengue infection. Furthermore, HCV treatment with interferon-alpha leads to specific MAIT cell activation in vivo in parallel with an enhanced therapeutic response. Moreover, TCR-independent activation of MAIT cells leads to a reduction of HCV replication in vitro mediated by IFN-gamma. Together these data demonstrate MAIT cells are activated following viral infections, and suggest a potential role in both host defence and immunopathology.

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