| Literature DB >> 28714991 |
Simon Rauber1, Markus Luber1, Stefanie Weber1, Lisa Maul1, Alina Soare1, Thomas Wohlfahrt1, Neng-Yu Lin1, Katharina Dietel1, Aline Bozec1, Martin Herrmann1, Mark H Kaplan2, Benno Weigmann3, Mario M Zaiss1, Ursula Fearon4, Douglas J Veale5, Juan D Cañete6, Oliver Distler7, Felice Rivellese8, Costantino Pitzalis8, Markus F Neurath3, Andrew N J McKenzie9, Stefan Wirtz3, Georg Schett1, Jörg H W Distler1, Andreas Ramming1.
Abstract
Inflammatory diseases such as arthritis are chronic conditions that fail to resolve spontaneously. While the cytokine and cellular pathways triggering arthritis are well defined, those responsible for the resolution of inflammation are incompletely characterized. Here we identified interleukin (IL)-9-producing type 2 innate lymphoid cells (ILC2s) as the mediators of a molecular and cellular pathway that orchestrates the resolution of chronic inflammation. In mice, the absence of IL-9 impaired ILC2 proliferation and activation of regulatory T (Treg) cells, and resulted in chronic arthritis with excessive cartilage destruction and bone loss. In contrast, treatment with IL-9 promoted ILC2-dependent Treg activation and effectively induced resolution of inflammation and protection of bone. Patients with rheumatoid arthritis in remission exhibited high numbers of IL-9+ ILC2s in joints and the circulation. Hence, fostering IL-9-mediated ILC2 activation may offer a novel therapeutic approach inducing resolution of inflammation rather than suppression of inflammatory responses.Entities:
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Year: 2017 PMID: 28714991 PMCID: PMC5575995 DOI: 10.1038/nm.4373
Source DB: PubMed Journal: Nat Med ISSN: 1078-8956 Impact factor: 53.440