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In vivo relationship between collagenase-2 and interleukin-8 but not tumour necrosis factor-α in chronic rhinosinusitis with nasal polyposis
被引:27
|作者:
Kostamo, K
Sorsa, T
Leino, M
Tervahartiala, T
Alenius, H
Richardson, M
Toskala, E
机构:
[1] Univ Helsinki, Cent Hosp, Dept Otorhinolaryngol, FIN-00029 Helsinki, Finland
[2] Univ Helsinki, Cent Hosp, Inst Dent, Dept Oral & Maxillofacial Dis, FIN-00029 Helsinki, Finland
[3] Univ Helsinki, Dept Occupat Med, Sect Otorhinolaryngol, Helsinki, Finland
[4] Univ Helsinki, Finnish Inst Occupat Hlth, Dept Toxicol, Helsinki, Finland
[5] Univ Helsinki, Haartman Inst, Dept Bacteriol & Immunol, Helsinki, Finland
来源:
关键词:
chronic rhinosinusitis;
interleukin-8;
matrix metalloproteinase-8;
nasal polyposis;
tumour necrosis factor-alpha;
D O I:
10.1111/j.1398-9995.2005.00888.x
中图分类号:
R392 [医学免疫学];
学科分类号:
100102 ;
摘要:
Background: The characteristic feature of chronic rhinosinusitis with nasal polyposis (CRSwNP) is eosinophilic inflammation of the sinus mucosa; a type of inflammation also seen in asthmatic airways. Similar histopathologic findings of airway remodelling are present in both diseases. Remodelling is tightly controlled by matrix metalloproteinases (MMP). Increase of collagenase-2 (MMP-8) expression in the bronchial epithelial cells has been described in asthmatic patients, but it has not been studied in CRSwNP. Methods: The concentrations and degree of activation of MMP-8 were analysed by immunofluorometric assay and Western blotting, respectively, in sinus mucus samples from CRSwNP patients and in nasal lavages from healthy controls in relation to inductive cytokines interleukin-8 (IL-8) and tumour necrosis factor-alpha (TNF-alpha). Results: Significantly elevated levels of MMP-8 and IL-8 but not TNF-alpha were found in CRSwNP patients relative to controls. In particular, the activation of mesenchymal-type MMP-8 but not polymorphonuclear-type MMP-8 was associated with elevated IL-8 levels. Conclusions: The IL-8 and MMP-8 seemingly form an inductive cytokine-proteinase cascade in CRSwNP pathogenesis. Together they provide a target for novel therapies and a diagnostic tool for monitoring CRSwNP treatment.
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页码:1275 / 1279
页数:5
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