- Goswami, Sangeeta;
- Angkasekwinai, Pornpimon;
- Shan, Ming;
- Greenlee, Kendra J;
- Barranco, Wade T;
- Polikepahad, Sumanth;
- Seryshev, Alexander;
- Song, Li-zhen;
- Redding, David;
- Singh, Bhupinder;
- Sur, Sanjiv;
- Woodruff, Prescott;
- Dong, Chen;
- Corry, David B;
- Kheradmand, Farrah
The innate immune response of airway epithelial cells to airborne allergens initiates the development of T cell responses that are central to allergic inflammation. Although proteinase allergens induce the expression of interleukin 25, we show here that epithelial matrix metalloproteinase 7 (MMP7) was expressed during asthma and was required for the maximum activity of interleukin 25 in promoting the differentiation of T helper type 2 cells. Allergen-challenged Mmp7(-/-) mice had less airway hyper-reactivity and production of allergic inflammatory cytokines and higher expression of retinal dehydrogenase 1. Inhibition of retinal dehydrogenase 1 restored the asthma phenotype of Mmp7(-/-) mice and inhibited the responses of lung regulatory T cells, whereas exogenous administration of retinoic acid attenuated the asthma phenotype. Thus, MMP7 coordinates allergic lung inflammation by activating interleukin 25 while simultaneously inhibiting retinoid-dependent development of regulatory T cells.