Development of a Mouse Model for Chronic Cat Allergen-Induced Asthma

被引:10
|
作者
Grundstrom, Jeanette [1 ]
Saarne, Tiiu [1 ]
Kemi, Cecilia [2 ,3 ]
Gregory, Joshua A. [2 ,3 ]
Waden, Konrad [1 ]
Pils, Marina C. [5 ]
Adner, Mikael [2 ,3 ]
Gafvelin, Guro [1 ,4 ]
van Hage, Marianne [1 ]
机构
[1] Karolinska Univ Hosp, Karolinska Inst, Dept Med, Clin Immunol & Allergy Unit, SE-17176 Stockholm, Sweden
[2] Karolinska Inst, Inst Environm Med, S-10401 Stockholm, Sweden
[3] Ctr Allergy Res, Stockholm, Sweden
[4] Dept Clin Neurosci, Therapeut Immune Design Unit, Stockholm, Sweden
[5] Helmholtz Ctr Infect Res, Mouse Pathol Anim Expt Unit, Braunschweig, Germany
基金
瑞典研究理事会;
关键词
Asthma; Allergy; Mouse model; Cat allergen; Fel d 1; FEL D 1; DUST-MITE; AIRWAY INFLAMMATION; GROWTH-FACTOR; RESPONSES; IMMUNOTHERAPY; EXPOSURE; MICE; SENSITIZATION; CHALLENGE;
D O I
10.1159/000369066
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Allergic asthma is a chronic inflammatory airway disease caused by exposure to airborne allergens. In order to develop novel therapies for allergic asthma, models that are relevant to human disease are needed. Methods: Female BALB/c mice were presensitised subcutaneously with alum-adsorbed recombinant cat allergen Fel d 1, followed by intranasal challenges with cat dander extract spiked with recombinant Fel d 1 for 7 weeks. For reference, mice were presensitised and challenged with ovalbumin following the same protocol. Airway hyperresponsiveness, serum antibodies, airway inflammation and cell infiltration, and cytokines in lung tissue and bronchoalveolar lavage were measured. Results: Mice presensitised with recombinant Fel d 1 and challenged with cat dander extract or presensitised and challenged with ovalbumin showed airway hyperresponsiveness in response to metacholine. Mice of the cat allergen model showed influx of neutrophils, eosinophils and lymphocytes in bronchoalveolar lavage, combined with increased levels of IL-17a and increased IL-4 mRNA expression in lung tissue. In contrast, mice sensitised and challenged with ovalbumin showed a predominant influx of eosinophils in bronchoalveolar lavage and had an increased expression of IL-5 in lung tissue. Both protocols induced features of lung tissue remodelling and allergen-specific antibody responses. Conclusions: The presented mouse model for cat allergen-induced asthma exhibits hallmarks of chronic allergic asthma, like airway hyperresponsiveness, a mixed neutrophilic/eosinophilic infiltration in bronchoalveolar lavage, expression of IL-17a and signs of remodelling in lung tissue. The model will provide a relevant platform for the development of novel treatment strategies. (C) 2014 S. Karger AG, Basel
引用
收藏
页码:195 / 205
页数:11
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