Key mediators in the immunopathogenesis of allergic asthma

被引:106
作者
Hall, Sannette
Agrawal, Devendra K.
机构
[1] Creighton Univ, Sch Med, Dept Biomed Sci, Omaha, NE 68178 USA
[2] Creighton Univ, Sch Med, Ctr Clin &Translat Sci, Omaha, NE 68178 USA
基金
美国国家卫生研究院;
关键词
Airway epithelium; Airway hyper-responsiveness; Allergic airway inflammation; Asthma; Innate lymphoid cells; Th17; cells; INNATE LYMPHOID-CELLS; REGULATORY T-CELLS; THYMIC STROMAL LYMPHOPOIETIN; SURFACTANT-PROTEIN-D; EOSINOPHILIC AIRWAY INFLAMMATION; HISTAMINE H-4 RECEPTOR; GROWTH-FACTOR-BETA; MAST-CELLS; DENDRITIC CELLS; ACTIVIN-A;
D O I
10.1016/j.intimp.2014.05.034
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Asthma is described as a chronic inflammatory disorder of the conducting airways. It is characterized by reversible airway obstruction, eosinophil and Th2 infiltration, airway hyper-responsiveness and airway remodeling. Our findings to date have largely been dependent on work done using animal models, which have been instrumental in broadening our understanding of the mechanism of the disease. However, using animals to model a uniquely human disease is not without its drawbacks. This review aims to examine some of the key mediators and cells of allergic asthma learned from animal models and shed some light on emerging mediators in the pathogenesis allergic airway inflammation in acute and chronic asthma. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:316 / 329
页数:14
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