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

  • Stephan Meller
  • , Jeremy Di Domizio
  • , Kui S. Voo
  • , Heike C. Friedrich
  • , Georgios Chamilos
  • , Dipyaman Ganguly
  • , Curdin Conrad
  • , Josh Gregorio
  • , Didier Le Roy
  • , Thierry Roger
  • , John E. Ladbury
  • , Bernhard Homey
  • , Stanley Watowich
  • , Robert L. Modlin
  • , Dimitrios P. Kontoyiannis
  • , Yong Jun Liu
  • , Stefan T. Arold
  • , Michel Gilliet

Research output: Contribution to journalArticlepeer-review

Abstract

Interleukin 17-producing helper T cells (TH 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 TH17 cell-derived cytokine, is a cationic amphipathic protein that kills extracellular bacteria via membrane-pore formation. Furthermore, TH17 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 TH17 cells by showing that IL-26 is a natural human antimicrobial that promotes immune sensing of bacterial and host cell death.

Original languageEnglish (US)
Pages (from-to)970-979
Number of pages10
JournalNature Immunology
Volume16
Issue number9
DOIs
StatePublished - Aug 19 2015

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

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