Authors:
TYF Halim, BMJ Rana, JA Walker, B Kerscher, MD Knolle, HE Jolin, EM Serrao, L Haim-Vilmovsky, SA Teichmann, H-R Rodewald, M Botto, TJ Vyse, PG Fallon, Z Li, DR Withers, ANJ McKenzie
Journal name: 
Immunity
Citation info: 
48(6):1195-1207.e6
Abstract: 
The local regulation of type 2 immunity relies on dialog between the epithelium and the innate and adaptive immune cells. Here we found that alarmin-induced expression of the co-stimulatory molecule OX40L on group 2 innate lymphoid cells (ILC2s) provided tissue-restricted T cell co-stimulation that was indispensable for Th2 and regulatory T (Treg) cell responses in the lung and adipose tissue. Interleukin (IL)-33 administration resulted in organ-specific surface expression of OX40L on ILC2s and the concomitant expansion of Th2 and Treg cells, which was abolished upon deletion of OX40L on ILC2s (Il7raCre/+Tnfsf4fl/fl mice). Moreover, Il7raCre/+Tnfsf4fl/fl mice failed to mount effective Th2 and Treg cell responses and corresponding adaptive type 2 pulmonary inflammation arising from Nippostrongylus brasiliensis infection or allergen exposure. Thus, the increased expression of OX40L in response to IL-33 acts as a licensing signal in the orchestration of tissue-specific adaptive type 2 immunity, without which this response fails to establish.
DOI: 
http://doi.org/10.1016/j.immuni.2018.05.003
Research group: 
Halim Group
E-pub date: 
19 Jun 2018