IL-18 modulates chronic fungal asthma in a murine model; putative involvement of Toll-like receptor-2

被引:44
作者
Blease, K [1 ]
Kunkel, SL [1 ]
Hogaboam, CM [1 ]
机构
[1] Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA
关键词
infectious immunity; fungi; allergy; lung; inflammatory mediators;
D O I
10.1007/PL00000233
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Fungus-induced asthmatic disease is characterized by persistent airway hyperreactivity and remodeling. Objective and design: To determine the role of IL-18 in the allergic airway response to Aspergillus fumigatus conidia in a murine model of A. fumigatus-induced asthma. Methods: A. fumigatus-sensitized mice were depleted of IL-18 using a polyclonal anti-IL-18 antibody for 3 days after a conidia challenge. Results: Airway hyperresponsiveness and eosinophil numbers were significantly elevated 3-30 days after conidia challenge compared to the normal serum-treated group. Histological evidence showed retention of A. fumigatus conidia, airway remodeling, subepithelial fibrosis, and increased collagen deposition in the lungs of IL-18-depleted mice at day 30 after the conidia challenge. Prolonged retention of conidia in IL-18 depleted A. Jumigatus-sensitized mice was associated with decreased Toll-like receptor-2 (TLR-2) expression compared with the control group. Conclusions: IL-18 modulates the innate immune response against A. fumigatus conidia and prevents the development of severe fungus-induced asthmatic disease.
引用
收藏
页码:552 / 560
页数:9
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