Relationships Between Eosinophilic Inflammation, Tissue Remodeling, and Fibrosis in Eosinophilic Esophagitis

被引:116
作者
Aceves, Seema S. [2 ,3 ,4 ]
Ackerman, Steven J. [1 ,5 ]
机构
[1] Univ Illinois, Coll Med, Dept Biochem & Mol Genet, Chicago, IL 60607 USA
[2] Rady Childrens Hosp, Div Allergy & Immunol, San Diego, CA 92123 USA
[3] Univ Calif, Dept Pediat, Div Allergy & Immunol, La Jolla, CA 92093 USA
[4] Univ Calif, Dept Med, Div Allergy & Immunol, La Jolla, CA 92093 USA
[5] Univ Illinois, Dept Med, Chicago, IL 60607 USA
基金
美国国家卫生研究院;
关键词
Eosinophilic esophagitis; Eosinophils; Inflammation; Remodeling; Fibrosis; Angiogenesis; Transforming growth factor-beta; MAJOR BASIC-PROTEIN; ENDOTHELIAL GROWTH-FACTOR; GASTROESOPHAGEAL-REFLUX DISEASE; ASTHMATIC AIRWAY INFLAMMATION; MUSCARINIC RECEPTOR FUNCTION; CHALLENGED GUINEA-PIGS; HUMAN ATOPIC SKIN; BRONCHIAL-ASTHMA; GENE-EXPRESSION; PULMONARY-FIBROSIS;
D O I
10.1016/j.iac.2008.10.003
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
The clinical and pathologic features of eosinophilic esophagitis (EE) include extensive tissue remodeling. Increasing evidence supports a key role for the eosinophil in multiple aspects of the esophageal remodeling and fibrosis seen in this allergic disease. This article reviews the clinical implications of esophageal remodeling and fibrosis in EE and discusses the possible pathogenic mechanisms inducing and regulating these responses. The focus is specifically on eosinophil and cytokine interactions with the esophageal epithelium, vascular enclothelium, resident fibroblasts, and smooth muscle. Current and potential therapeutic interventions are discussed that may impact the development or resolution of chronic esophageal remodeling and fibrosis in EE.
引用
收藏
页码:197 / +
页数:17
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