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