IL-22 induces Reg3γ and inhibits allergic inflammation in house dust mite-induced asthma models

被引:41
作者
Ito, Takashi [1 ]
Hirose, Koichi [1 ]
Saku, Aiko [1 ]
Kono, Kenta [1 ]
Takatori, Hiroaki [1 ]
Tamachi, Tomohiro [1 ]
Goto, Yoshiyuki [2 ]
Renauld, Jean-Christophe [4 ,5 ]
Kiyono, Hiroshi [3 ,6 ,7 ]
Nakajima, Hiroshi [1 ]
机构
[1] Chiba Univ, Grad Sch Med, Dept Allergy & Clin Immunol, Chiba, Japan
[2] Chiba Univ, Med Mycol Res Ctr, Div Mol Immunol, Chiba, Japan
[3] Chiba Univ, Grad Sch Med, Dept Immunol, Chiba, Japan
[4] Ludwig Inst Canc Res, Brussels Branch, Brussels, Belgium
[5] Catholic Univ Louvain, de Duve Inst, Brussels, Belgium
[6] Univ Tokyo, Int Res & Dev Ctr Mucosal Vaccines, Tokyo, Japan
[7] Univ Tokyo, Inst Med Sci, Div Mucosal Immunol, Tokyo, Japan
关键词
EPITHELIAL-CELLS; HOST-DEFENSE; AIRWAY INFLAMMATION; TH17; CELLS; INTERLEUKIN-22; MICE; DIFFERENTIATION; MACROPHAGES; MICROBIOTA; EXPRESSION;
D O I
10.1084/jem.20162108
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Previous studies have shown that IL-22, one of the Th17 cell-related cytokines, plays multiple roles in regulating allergic airway inflammation caused by antigen-specific Th2 cells; however, the underlying mechanism remains unclear. Here, we show that allergic airway inflammation and Th2 and Th17 cytokine production upon intratracheal administration of house dust mite (HDM) extract, a representative allergen, were exacerbated in IL-22-deficient mice. We also found that IL-22 induces Reg3. production from lung epithelial cells through STAT3 activation and that neutralization of Reg3. significantly exacerbates HDM-induced eosinophilic airway inflammation and Th2 cytokine induction. Moreover, exostatin-like 3 (EXTL3), a functional Reg3. binding protein, is expressed in lung epithelial cells, and intratracheal administration of recombinant Reg3. suppresses HDM-induced thymic stromal lymphopoietin and IL-33 expression and accumulation of type 2 innate lymphoid cells in the lung. Collectively, these results suggest that IL-22 induces Reg3. production from lung epithelial cells and inhibits the development of HDM-induced allergic airway inflammation, possibly by inhibiting cytokine production from lung epithelial cells.
引用
收藏
页码:3037 / 3050
页数:14
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