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


Autoria(s): Meller S.; Di Domizio J.; Voo K.S.; Friedrich H.C.; Chamilos G.; Ganguly D.; Conrad C.; Gregorio J.; Le Roy D.; Roger T.; Ladbury J.E.; Homey B.; Watowich S.; Modlin R.L.; Kontoyiannis D.P.; Liu Y.J.; Arold S.T.; Gilliet M.
Data(s)

2015

Resumo

Interleukin 17-producing helper T cells (TH17 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.

Identificador

http://serval.unil.ch/?id=serval:BIB_8915C0704772

isbn:1529-2916 (Electronic)

pmid:26168081

doi:10.1038/ni.3211

isiid:000359876900015

Idioma(s)

en

Fonte

Nature Immunology, vol. 16, no. 9, pp. 970-979

Tipo

info:eu-repo/semantics/article

article