Mechanisms of eosinophilia in the pathogenesis of hypereosinophilic disorders

被引:91
作者
Ackerman, Steven J.
Bochner, Bruce S.
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Div Clin Immunol & Allergy, Baltimore, MD 21224 USA
[2] Univ Illinois, Coll Med, Dept Biochem & Mol Genet, Chicago, IL 60607 USA
关键词
FC-EPSILON-RI; MAJOR BASIC-PROTEIN; GROWTH-FACTOR-BETA; ANTI-IL-5 MEPOLIZUMAB THERAPY; COLONY-STIMULATING FACTOR; AFFINITY IGE RECEPTOR; BONE-MARROW; GENE-EXPRESSION; MURINE MODEL; IN-VITRO;
D O I
10.1016/j.iac.2007.07.004
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
The increased numbers of activated eosinophils in the blood and tissues that typically accompany hypereosinophilic disorders result from a variety of mechanisms. Exciting advances in translating discoveries achieved from mouse models and molecular strategies to the clinic have led to a flurry of new therapeutics specifically designed to target eosinophil-associated diseases. So far, this form of hypothesis testing in humans in vivo through pharmacology generally has supported the paradigms generated in vitro and in animal models, raising hopes that a spectrum of novel therapies soon may become available to help those who have eosinophil-associated diseases.
引用
收藏
页码:357 / +
页数:21
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