Literature DB >> 15463816

Cell and cytokine profile in nasal secretions in cystic fibrosis.

Cyrille Bergoin1, Philippe Gosset, Catherine Lamblin, Florence Bolard, Dominique Turck, André Bernard Tonnel, Benoît Wallaert.   

Abstract

BACKGROUND: Nasal polyposis (NP) frequently complicates the course of cystic fibrosis (CF). The aim of this study was to determine the pattern of inflammatory cells and mediators in nasal secretions from patients with or without NP compared to patients with idiopathic NP and healthy controls.
METHODS: Eighteen CF patients with NP (NP+ group: 6 untreated, 12 treated with nasal steroids), and 15 without NP (NP- group) were included in this prospective study and compared to 9 patients with idiopathic NP and 12 healthy controls. Differential cell count eosinophil cationic protein (ECP), interleukin-5 (IL-5) and IL-8 were determined in nasal lavage fluids.
RESULTS: The total cell count, the number and the percentage of neutrophils and eosinophils, the levels of IL-8, IL-5 and ECP were significantly higher in nasal secretions from both NP+ and NP- as compared with controls. No difference was found between untreated and treated CF patients with NP. No difference was found between NP+ and NP- groups. Compared to idiopathic NP group, both NP+ and NP- groups had higher percentage of neutrophils and lower percentage of eosinophils. There were no differences according to the use of topical steroids, systemic antibiotherapy, or the type of mutation. CF patients with positive nasal culture had a higher percentage of neutrophils than those with negative culture. CF patients with atopy had a higher percentage of eosinophils than non-atopic patients.
CONCLUSION: Our results demonstrate that nasal inflammation is a prominent feature in patients with CF and does not differ according to the presence of NP. IL-8 and IL-5 may play crucial roles in recruitment and activation of neutrophils and eosinophils in upper airways of CF patients.

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Year:  2002        PMID: 15463816     DOI: 10.1016/s1569-1993(02)00072-3

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.482


  10 in total

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2.  Cystic fibrosis: ultrastructural changes of nasal mucosa.

Authors:  Stephan Knipping; Hans Juergen Holzhausen; Andreas Riederer; Marc Bloching
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3.  Quantitative analysis of nasal transcripts reveals potential biomarkers for Parkinson's disease.

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4.  Salivary Cytokines and Airways Disease Severity in Patients with Cystic Fibrosis.

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Review 5.  Mechanisms of the noxious inflammatory cycle in cystic fibrosis.

Authors:  Mathilde Rottner; Jean-Marie Freyssinet; M Carmen Martínez
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6.  Reduced nasal nitric oxide production in cystic fibrosis patients with elevated systemic inflammation markers.

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7.  Dynamics of soluble and cellular inflammatory markers in nasal lavage obtained from cystic fibrosis patients during intravenous antibiotic treatment.

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8.  Neutrophil extracellular traps are present in the airways of ENaC-overexpressing mice with cystic fibrosis-like lung disease.

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9.  Copper-Associated Oxidative Stress Contributes to Cellular Inflammatory Responses in Cystic Fibrosis.

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Journal:  Biomedicines       Date:  2021-03-24

10.  Cytokine profile in subjects with Cystic Fibrosis and nasal polyposis compared to patients with no nasal disorders.

Authors:  Flávio Barbosa Nunes; Mirian Cabral Moreira de Castro; Tacimara Moreira da Silva; Ricardo Nascimento Araújo; Helena Maria Gonçalves Becker; Paulo Fernando Tormin Borges Crosara; Roberto Eustáquio Santos Guimarães
Journal:  Braz J Otorhinolaryngol       Date:  2010 Jan-Feb
  10 in total

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