Effect of suplatast tosilate, a Th2 cytokine inhibitor, on cough variant asthma
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- 作者：Takanobu Shioya ; Masahiro Satake ; Masaaki Sano ; Manabu Kagaya ; Akiko Watanabe ; Kazuhiro Sato ; Takeshi Ito ; Nobuaki Ito ; Masahiro Sasaki and Mamoru Miura
- 刊名：European Journal of Clinical Pharmacology
- 出版时间：June 2002
- 出版年：2002
- 期刊代码：82_0031-6970
- 类别：bio
- 卷：58
- 期：3
- 页码：171-176
- 数据来源：sp
摘要
Study objective. Th2 cytokines play an important role in the pathogenesis of asthma. Our study objective was to determine the effect of suplatast tosilate, a Th2 cytokine inhibitor, on patients with cough-variant asthma. Methods. Twenty patients with cough-variant asthma (CVA) were assigned to a suplatast tosilate (100 mg three times daily) group or a placebo group for 6 weeks in a double-blind randomized study. The cough scores, medication scores, pulmonary function, bronchial hyperresponsiveness to methacholine, cough threshold for capsaicin, percentage of eosinophils and concentrations of eosinophilic cationic protein (ECP) in hypertonic saline-induced (induced) sputum were evaluated. The main outcome measures were capsaicin cough threshold and concentrations of ECP in induced sputum. Results. In the suplatast group, the cough scores and the medication scores decreased significantly over time. The percentage of eosinophils in induced sputum significantly decreased from 53.5LJ.6%to 13.6DŽ.6%. The cough threshold for capsaicin improved significantly from 2.72Dž.41 µM to 39.7ᆪ.7 µM in the suplatast group. The concentrations of ECP in induced sputum decreased significantly from 435끃 µg/l to 56ᆶ µg/l in the suplatast group. The bronchial responsiveness to methacholine changed from 8.45Dž.43 units to 11.4Dž.76 units in the suplatast group. Conclusions. Suplatast improved the cough scores and the cough threshold for capsaicin in patients with CVA without significant side effects, suggesting the effectiveness of suplatast in the treatment of CVA. Suplatast also decreased the percentage of eosinophils and concentrations of ECP in induced sputum, suggesting improvement in eosinophilic inflammation in patients with CVA. Further pharmacodynamic research is needed to explain the precise mechanism.