Epinastine inhibits eosinophil chemotaxis and adhesion molecules in atopic dermatitis

被引:11
作者
Matsukura, M
Yajima, A
Yamazaki, F
Yudate, T
Yamada, H
Tezuka, T
机构
[1] Kinki Univ, Sch Med, Dept Dermatol, Osaka 5898511, Japan
[2] Kinki Univ, Nara Hosp, Dept Dermatol, Nara 631, Japan
来源
SKIN PHARMACOLOGY AND APPLIED SKIN PHYSIOLOGY | 2003年 / 16卷 / 06期
关键词
adhesion molecule; antiallergic drug; atopic dermatitis; CD11b; chemotaxis; cyokine; eosinophils; eotaxin; epinastine; interleukin-5;
D O I
10.1159/000072936
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Purpose: To investigate the effects of epinastine on eosinophil chemotaxis and changes in eosinophil adhesion molecules induced by epinastine and three other antiallergic agents, using eosinophils of atopic dermatitis (AD) patients. Results: Epinastine reduced eosinophil chemotaxis toward eotaxin when the eosinophils had been prestimulated with interleukin (IL)-5, but given alone it did not alter eosinophil chemotaxis toward IL-5. CD11b expression was inhibited when peripheral blood was prestimulated with IL-5, but eosinophil adhesion molecule expression was not altered. Conclusions: Epinastine suppresses allergic inflammation not only through its strong antihistamine and antimediator effects, but also by inhibiting eosinophilic chemotaxis and the expression of adhesion molecules involved in chemotaxis, especially CD11b. Copyright (C) 2003 S. Karger AG, Basel.
引用
收藏
页码:405 / 410
页数:6
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