Neutralizing Antibody Against Granulocyte/Macrophage Colony-Stimulating Factor Inhibits Inflammatory Response in Experimental Otitis Media

被引:9
|
作者
Kariya, Shin [1 ]
Okano, Mitsuhiro [1 ]
Higaki, Takaya [1 ]
Makihara, Seiichiro [1 ]
Haruna, Takenori [1 ]
Eguchi, Motoharu [1 ]
Nishizaki, Kazunori [1 ]
机构
[1] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Otolaryngol Head & Neck Surg, Okayama 7008558, Japan
来源
LARYNGOSCOPE | 2013年 / 123卷 / 06期
关键词
Granulocyte/macrophage colony-stimulating factor; middle ear; otitis; cytokine; chemokine; lipopolysaccharide; endotoxin; GM-CSF; EFFUSION; CYTOKINES; MICE; CELLS; TNF;
D O I
10.1002/lary.23795
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Objectives/Hypothesis: Granulocyte/macrophage colony-stimulating factor is important in the pathogenesis of acute and chronic inflammatory disease. We hypothesized that granulocyte/macrophage colony-stimulating factor plays a pivotal role in middle ear inflammation and that neutralization of granulocyte/macrophage colony-stimulating factor would inhibit neutrophil migration into the middle ear and production of inflammatory mediators. Study Design: Animal experiment. Methods: We used transtympanic administration of lipopolysaccharide, a major component of gram-negative bacteria, into mice to induce an experimental otitis media. Control mice received injection of phosphate-buffered saline into the middle ear cavity. Mice were systemically treated with granulocyte/macrophage colony-stimulating factor neutralizing antibody or control immunoglobulin G via intraperitoneal injection 2 hours before transtympanic injection of lipopolysaccharide or phosphate-buffered saline. Middle ear effusions were collected. Concentrations of interleukin (IL)-1 beta, tumor necrosis factor (TNF)-alpha, keratinocyte chemoattractant, and macrophage inflammatory protein-2 in middle ear effusions were measured by enzyme-linked immunosorbent assay. Histologic examination of the middle ear was also performed. Results: Transtympanic injection of lipopolysaccharide upregulated levels of granulocyte/macrophage colony-stimulating factor, IL-1 beta, TNF-alpha, keratinocyte chemoattractant, and macrophage inflammatory protein-2 in the middle ear. Concentrations of cytokines and chemokines were significantly decreased in mice injected with granulocyte/macrophage colony-stimulating factor neutralizing antibody. Infiltration of inflammatory cells into the middle ear cavity induced by lipopolysaccharide was also significantly reduced by neutralization of granulocyte/macrophage colony-stimulating factor. Conclusions: Systemic injection of granulocyte/macrophage colony-stimulating factor neutralizing antibody inhibits the middle ear inflammation induced by lipopolysaccharide in mice. Our findings suggest that granulocyte/macrophage colony-stimulating factor may offer a novel therapeutic target for the management of intractable otitis media.
引用
收藏
页码:1514 / 1518
页数:5
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