Allergic airway inflammation

被引:24
作者
Agrawal, DK
Bharadwaj, A
机构
[1] Creighton Univ, Sch Med, Dept Biomed Sci, Omaha, NE 68178 USA
[2] Creighton Univ, Sch Med, Dept Med, Omaha, NE 68178 USA
[3] Creighton Univ, Sch Med, Dept Med Microbiol & Immunol, Omaha, NE 68178 USA
关键词
D O I
10.1007/s11882-005-0088-7
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Several genes, including ADAM33, DPP10, PHFI I, GPRA, and TIM-I, have been implicated in the pathogenesis and susceptibility to atopy and asthma. Advances have been made in defining the mechanism for the control of allergic airway inflammation in response to inhaled antigens. There is growing evidence that associates asthma with a systemic propensity for allergic type 2 T-cell cytokines. Disordered coagulation and fibrinolysis could also exacerbate asthma symptoms. Major emphasis on immunotherapy for asthma during the past decade has been to direct the immune response to a type I response. Recent literature supports the pivotal role of plasmacytoid dendritic cells and allergen-specific T-regulatory cells in the development of tolerance to allergens. In this review article, we discuss the current information on the pathogenesis of allergic airway inflammation and potential allergen immunotherapies, which could be beneficial in the treatment of airway inflammation, allergy, and asthma.
引用
收藏
页码:142 / 148
页数:7
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