Long-Term Exposure to House Dust Mite Leads to the Suppression of Allergic Airway Disease Despite Persistent Lung Inflammation

被引:33
作者
Bracken, Sonali J. [1 ]
Adami, Alexander J. [1 ]
Szczepanek, Steven M. [3 ]
Ehsan, Mohsin [2 ]
Natarajan, Prabitha [1 ]
Guernsey, Linda A. [1 ]
Shahriari, Neda [1 ]
Rafti, Ektor [4 ]
Matson, Adam P. [4 ]
Schramm, Craig M. [4 ]
Thrall, Roger S. [1 ,2 ]
机构
[1] Univ Connecticut, Ctr Hlth, Dept Immunol, Farmington, CT 06030 USA
[2] Univ Connecticut, Ctr Hlth, Dept Med, Farmington, CT 06030 USA
[3] Univ Connecticut, Ctr Hlth, Neag Comprehens Canc Ctr, Farmington, CT 06030 USA
[4] Connecticut Childrens Med Ctr, Dept Pediat, Hartford, CT USA
关键词
Airway eosinophilia; Airway hyperreactivity; Chronic allergen challenge; House dust mite; Macrophages; REGULATORY T-CELLS; MURINE ASTHMA MODEL; MULTINUCLEATED GIANT-CELLS; COLONY-STIMULATING FACTOR; INHALATIONAL TOLERANCE; LYMPH-NODES; MICE; ANTIGEN; RESPONSES; HYPERRESPONSIVENESS;
D O I
10.1159/000381058
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Allergic asthma is a major cause of worldwide morbidity and results from inadequate immune regulation in response to innocuous, environmental antigens. The need exists to understand the mechanisms that promote nonreactivity to human-relevant allergens such as house dust mite (HDM) in order to develop curative therapies for asthma. The aim of our study was to compare the effects of short-, intermediate-and long-term HDM administration in a murine asthma model and determine the ability of long-term HDM exposure to suppress allergic inflammation. Methods: C57BL/6 mice were intranasally instilled with HDM for short-term (2 weeks), intermediate-term (5 weeks) and long-term (11 weeks) periods to induce allergic airway disease (AAD). The severity of AAD was compared across all stages of the model via both immunological and pulmonary parameters. Results: Short-and intermediate-term HDM exposure stimulated the development of AAD that included eosinophilia in the bronchoalveolar lavage fluid (BALF), pronounced airway hyperreactivity (AHR) and evidence of lung inflammation. Long-term HDM exposure promoted the suppression of AAD, with a loss of BALF eosinophilia and AHR despite persistent mononuclear inflammation in the lungs. Suppression of AAD with long-term HDM exposure was associated with an increase in both Foxp3+ regulatory T cells and IL-10-positive alveolar macrophages at the site of inflammation. Conclusions: This model recapitulates the key features of human asthma and may facilitate investigation into the mechanisms that promote immunological tolerance against clinically relevant aeroallergens. (C) 2015 S. Karger AG, Basel
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收藏
页码:243 / 258
页数:16
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