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Gender comparison in a murine model of allergen-driven airway inflammation and the response to budesonide treatment

BACKGROUND: Evidence suggests that gender differences exist in the severity of many immunological diseases and their response to glucocorticosteroid treatment. In this report, we have used a murine model of ovalbumin-induced lung inflammation to address whether gender could affect the systemic respo...

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Autores principales: Corteling, Randolph, Trifilieff, Alexandre
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC406499/
https://www.ncbi.nlm.nih.gov/pubmed/15086961
http://dx.doi.org/10.1186/1471-2210-4-4
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author Corteling, Randolph
Trifilieff, Alexandre
author_facet Corteling, Randolph
Trifilieff, Alexandre
author_sort Corteling, Randolph
collection PubMed
description BACKGROUND: Evidence suggests that gender differences exist in the severity of many immunological diseases and their response to glucocorticosteroid treatment. In this report, we have used a murine model of ovalbumin-induced lung inflammation to address whether gender could affect the systemic response, airway inflammation and hyperreactivity and their responses to budesonide. RESULTS: Following an acute ovalbumin challenge, actively sensitised BALB/c mice developed a time-dependent increase in interleukin-4 and interleukin-5 production and inflammatory cell influx into bronchoalveolar lavage fluid. Apart from an increased number of lymphocytes in female mice at day 3 post-challenge, none of the above parameters were affected by gender. Blood leukocyte numbers were also unaffected, whereas a two-fold increase in total serum immunoglobulin E was observed in female mice. Budesonide, given intranasally, did not affect the blood parameters, but dose-dependently inhibited the pulmonary inflammation and airway hyperreactivity in both male and female mice. Female mice were slightly less sensitive to budesonide's inhibitory action on interleukin-5 production and the development of airway hyperreactivity. CONCLUSIONS: Our results suggest that, apart from a 2-fold increase in serum immunoglobulin E levels observed in female mice, gender is not a major factor in the present murine model of ovalbumin-induced lung inflammation. In contrast, gender might slightly influence the potency of test compounds such as steroids.
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spelling pubmed-4064992004-05-13 Gender comparison in a murine model of allergen-driven airway inflammation and the response to budesonide treatment Corteling, Randolph Trifilieff, Alexandre BMC Pharmacol Research Article BACKGROUND: Evidence suggests that gender differences exist in the severity of many immunological diseases and their response to glucocorticosteroid treatment. In this report, we have used a murine model of ovalbumin-induced lung inflammation to address whether gender could affect the systemic response, airway inflammation and hyperreactivity and their responses to budesonide. RESULTS: Following an acute ovalbumin challenge, actively sensitised BALB/c mice developed a time-dependent increase in interleukin-4 and interleukin-5 production and inflammatory cell influx into bronchoalveolar lavage fluid. Apart from an increased number of lymphocytes in female mice at day 3 post-challenge, none of the above parameters were affected by gender. Blood leukocyte numbers were also unaffected, whereas a two-fold increase in total serum immunoglobulin E was observed in female mice. Budesonide, given intranasally, did not affect the blood parameters, but dose-dependently inhibited the pulmonary inflammation and airway hyperreactivity in both male and female mice. Female mice were slightly less sensitive to budesonide's inhibitory action on interleukin-5 production and the development of airway hyperreactivity. CONCLUSIONS: Our results suggest that, apart from a 2-fold increase in serum immunoglobulin E levels observed in female mice, gender is not a major factor in the present murine model of ovalbumin-induced lung inflammation. In contrast, gender might slightly influence the potency of test compounds such as steroids. BioMed Central 2004-04-15 /pmc/articles/PMC406499/ /pubmed/15086961 http://dx.doi.org/10.1186/1471-2210-4-4 Text en Copyright © 2004 Corteling and Trifilieff; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Research Article
Corteling, Randolph
Trifilieff, Alexandre
Gender comparison in a murine model of allergen-driven airway inflammation and the response to budesonide treatment
title Gender comparison in a murine model of allergen-driven airway inflammation and the response to budesonide treatment
title_full Gender comparison in a murine model of allergen-driven airway inflammation and the response to budesonide treatment
title_fullStr Gender comparison in a murine model of allergen-driven airway inflammation and the response to budesonide treatment
title_full_unstemmed Gender comparison in a murine model of allergen-driven airway inflammation and the response to budesonide treatment
title_short Gender comparison in a murine model of allergen-driven airway inflammation and the response to budesonide treatment
title_sort gender comparison in a murine model of allergen-driven airway inflammation and the response to budesonide treatment
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC406499/
https://www.ncbi.nlm.nih.gov/pubmed/15086961
http://dx.doi.org/10.1186/1471-2210-4-4
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