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.
机构:
RUTGERS STATE UNIV,COLL PHARM,DEPT PHARM PRACTICE & ADM,PISCATAWAY,NJ 08854RUTGERS STATE UNIV,COLL PHARM,DEPT PHARM PRACTICE & ADM,PISCATAWAY,NJ 08854
HOGAN, KR
PETERS, MD
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RUTGERS STATE UNIV,COLL PHARM,DEPT PHARM PRACTICE & ADM,PISCATAWAY,NJ 08854RUTGERS STATE UNIV,COLL PHARM,DEPT PHARM PRACTICE & ADM,PISCATAWAY,NJ 08854
机构:
Ludwig Inst Canc Res, Melbourne Tumour Biol Branch, PO Royal Melbourne Hosp, Melbourne, Vic 3050, AustraliaLudwig Inst Canc Res, Melbourne Tumour Biol Branch, PO Royal Melbourne Hosp, Melbourne, Vic 3050, Australia
Nice, Edouard
Dempsey, Peter
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Ludwig Inst Canc Res, Melbourne Tumour Biol Branch, PO Royal Melbourne Hosp, Melbourne, Vic 3050, AustraliaLudwig Inst Canc Res, Melbourne Tumour Biol Branch, PO Royal Melbourne Hosp, Melbourne, Vic 3050, Australia
Dempsey, Peter
Layton, Judith
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Ludwig Inst Canc Res, Melbourne Tumour Biol Branch, PO Royal Melbourne Hosp, Melbourne, Vic 3050, AustraliaLudwig Inst Canc Res, Melbourne Tumour Biol Branch, PO Royal Melbourne Hosp, Melbourne, Vic 3050, Australia
Layton, Judith
Morstyn, George
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Ludwig Inst Canc Res, Melbourne Tumour Biol Branch, PO Royal Melbourne Hosp, Melbourne, Vic 3050, AustraliaLudwig Inst Canc Res, Melbourne Tumour Biol Branch, PO Royal Melbourne Hosp, Melbourne, Vic 3050, Australia
Morstyn, George
Cui, Da-Fu
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Walter & Eliza Hall Inst Med Res, Ludwig Inst Canc Res, Joint Prot Struct Lab, Melbourne, Vic 3050, AustraliaLudwig Inst Canc Res, Melbourne Tumour Biol Branch, PO Royal Melbourne Hosp, Melbourne, Vic 3050, Australia
Cui, Da-Fu
Simpson, Richard
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Walter & Eliza Hall Inst Med Res, Ludwig Inst Canc Res, Joint Prot Struct Lab, Melbourne, Vic 3050, AustraliaLudwig Inst Canc Res, Melbourne Tumour Biol Branch, PO Royal Melbourne Hosp, Melbourne, Vic 3050, Australia
Simpson, Richard
Fabri, Louis
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Ludwig Inst Canc Res, Melbourne Tumour Biol Branch, PO Royal Melbourne Hosp, Melbourne, Vic 3050, AustraliaLudwig Inst Canc Res, Melbourne Tumour Biol Branch, PO Royal Melbourne Hosp, Melbourne, Vic 3050, Australia
Fabri, Louis
Burgess, Antony
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Ludwig Inst Canc Res, Melbourne Tumour Biol Branch, PO Royal Melbourne Hosp, Melbourne, Vic 3050, AustraliaLudwig Inst Canc Res, Melbourne Tumour Biol Branch, PO Royal Melbourne Hosp, Melbourne, Vic 3050, Australia