4.7 Article

TH17 cells promote microbial killing and innate immune sensing of DNA via interleukin 26

Journal

NATURE IMMUNOLOGY
Volume 16, Issue 9, Pages 970-979

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/ni.3211

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Funding

  1. Swiss National Science Foundation [144072, 149511]
  2. National Cancer Institute [CA128913]
  3. DANA Foundation
  4. German Research Foundation
  5. research commission of the Medical Faculty of the University of Dusseldorf
  6. King Abdullah University of Science and Technology (KAUST)

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Interleukin 17-producing helper T cells (T(H)17 cells) have a major role in protection against infections and in mediating autoimmune diseases, yet the mechanisms involved are incompletely understood. We found that interleukin 26 (IL-26), a human T(H)17 cell-derived cytokine, is a cationic amphipathic protein that kills extracellular bacteria via membrane-pore formation. Furthermore, T(H)17 cell-derived IL-26 formed complexes with bacterial DNA and self-DNA released by dying bacteria and host cells. The resulting IL-26-DNA complexes triggered the production of type I interferon by plasmacytoid dendritic cells via activation of Toll-like receptor 9, but independently of the IL-26 receptor. These findings provide insights into the potent antimicrobial and proinflammatory function of T(H)17 cells by showing that IL-26 is a natural human antimicrobial that promotes immune sensing of bacterial and host cell death.

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