Literature DB >> 17347573

Age-related difference in the persistency of allergic airway inflammation and bronchial hyperresponsiveness in a murine model of asthma.

Hiroo Mayuzumi1, Yasushi Ohki, Kenichi Tokuyama, Akira Sato, Takahisa Mizuno, Hirokazu Arakawa, Hiroyuki Mochizuki, Akihiro Morikawa.   

Abstract

AIM: Asthmatic children are more likely to outgrow their symptoms than adult patients. Thus, we wanted to know whether there were any age-related differences in the time course of the allergic airway inflammation.
METHODS: BALB/C mice at different ages (young: 3 days after birth, and mature: 8 weeks of age) were sensitized with ovalbumin (OVA). Subsequently, animals were challenged with aerosolized OVA during 1, 2, 4 or 8 consecutive weeks. Bronchial hyperresponsiveness (BHR), serum IgE levels, the degrees of inflammatory cell infiltration (ICI) and goblet cell metaplasia (GCM) in the airways, and the number of eosinophils and cytokine levels in bronchoalveolar lavage fluid (BALF) were examined.
RESULTS: At 1 week, airway inflammation and BHR occurred similarly between young and mature mice. However, BHR disappeared at 4 weeks in young, whereas it persisted even at 8 weeks in mature mice. GCM, ICI and eosinophilia in BALF attenuated with time, with more remarkable reduction in young mice. The BALF IL-4 level was high during the first 2 weeks in both groups, while the IL-2 level was significantly increased at 2 weeks solely in young mice.
CONCLUSION: Different time courses in airway inflammation and in BHR may relate to the different prognoses between childhood and adult asthma. The understanding of the mechanisms underlying this age-related differences may be helpful to induce remission in asthmatic patients. Copyright 2007 S. Karger AG, Basel.

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Year:  2007        PMID: 17347573     DOI: 10.1159/000100570

Source DB:  PubMed          Journal:  Int Arch Allergy Immunol        ISSN: 1018-2438            Impact factor:   2.749


  1 in total

1.  Pathophysiological features of asthma develop in parallel in house dust mite-exposed neonatal mice.

Authors:  Sejal Saglani; Sara A Mathie; Lisa G Gregory; Matthew J Bell; Andrew Bush; Clare M Lloyd
Journal:  Am J Respir Cell Mol Biol       Date:  2009-01-16       Impact factor: 6.914

  1 in total

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