Epinastine inhibits eosinophil chemotaxis and adhesion molecules in atopic dermatitis.

M Matsukura, A Yajima, F Yamazaki, T Yudate, H Yamada, T Tezuka
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引用次数: 13

Abstract

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.

Epinastine在特应性皮炎中抑制嗜酸性粒细胞趋化和粘附分子。
目的:以特应性皮炎(AD)患者嗜酸性粒细胞为研究对象,探讨嗜酸性粒细胞趋化性和嗜酸性粒细胞粘附分子变化对嗜酸性粒细胞和其他3种抗过敏药物的影响。结果:嗜酸性粒细胞在白细胞介素(IL)-5预刺激下,Epinastine降低嗜酸性粒细胞对eotaxin的趋化性,但单独给予Epinastine不改变嗜酸性粒细胞对IL-5的趋化性。白细胞介素-5预刺激外周血可抑制CD11b的表达,但不改变嗜酸性粒细胞粘附分子的表达。结论:Epinastine不仅通过其强大的抗组胺和抗介质作用抑制变应性炎症,而且通过抑制嗜酸性趋化和参与趋化的粘附分子尤其是CD11b的表达来抑制变应性炎症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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