| Literature DB >> 24717539 |
Takayuki Imanishi1, Chitose Ishihara1, Mohamed El Sherif Gadelhaq Badr1, Akiko Hashimoto-Tane1, Yayoi Kimura2, Taro Kawai3, Osamu Takeuchi3, Ken J Ishii4, Shun'ichiro Taniguchi5, Tetsuo Noda6, Hisashi Hirano2, Frank Brombacher7, Glen N Barber8, Shizuo Akira9, Takashi Saito10.
Abstract
While T-cell responses are directly modulated by Toll-like receptor (TLR) ligands, the mechanism and physiological function of nucleic acids (NAs)-mediated T cell costimulation remains unclear. Here we show that unlike in innate cells, T-cell costimulation is induced even by non-CpG DNA and by self-DNA, which is released from dead cells and complexes with antimicrobial peptides or histones. Such NA complexes are internalized by T cells and induce costimulatory responses independently of known NA sensors, including TLRs, RIG-I-like receptors (RLRs), inflammasomes and STING-dependent cytosolic DNA sensors. Such NA-mediated costimulation crucially induces Th2 differentiation by suppressing T-bet expression, followed by the induction of GATA-3 and Th2 cytokines. These findings unveil the function of NA sensing by T cells to trigger and amplify allergic inflammation.Entities:
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Year: 2014 PMID: 24717539 DOI: 10.1038/ncomms4566
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919