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酸性哺乳动物几丁质酶——哮喘治疗的潜在靶点。

Acidic mammalian chitinase--a potential target for asthma therapy.

作者信息

Donnelly Louise E, Barnes Peter J

机构信息

Thoracic Medicine, National Heart and Lung Institute, Dovehouse Street, London SW3 6LY, UK.

出版信息

Trends Pharmacol Sci. 2004 Oct;25(10):509-11. doi: 10.1016/j.tips.2004.08.002.

Abstract

Recently, inhibition of acidic mammalian chitinase in a murine asthmatic model was reported to have a profound anti-inflammatory effect, leading to the suggestion that this enzyme might be a novel therapeutic target for T helper 2-driven diseases such as asthma. The mechanism of action of such an enzyme in asthma pathology is unclear but the enzyme appears to mediate interleukin 13-dependent responses in a STAT6-independent manner. This observation has led to the proposal that chitinase family members are important mediators in allergic diseases including asthma.

摘要

最近,据报道在小鼠哮喘模型中抑制酸性哺乳动物几丁质酶具有显著的抗炎作用,这表明该酶可能是哮喘等由辅助性T细胞2驱动的疾病的新型治疗靶点。这种酶在哮喘病理中的作用机制尚不清楚,但该酶似乎以一种不依赖信号转导和转录激活因子6的方式介导白细胞介素13依赖性反应。这一观察结果促使人们提出,几丁质酶家族成员是包括哮喘在内的过敏性疾病的重要介质。

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