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用于治疗黏多糖贮积症II型的艾度硫酸酯酶

Idursulfase for the treatment of mucopolysaccharidosis II.

作者信息

Clarke Lorne A

机构信息

University of British Columbia and the Child and Family Research Institute, Department of Medical Genetics, 4500 Oak Street, Vancouver, British Columbia, Canada.

出版信息

Expert Opin Pharmacother. 2008 Feb;9(2):311-7. doi: 10.1517/14656566.9.2.311.

Abstract

Human recombinant proteins are being used to treat an increasing number of disorders. Advances in the large scale production of recombinant proteins and the understanding of glycosylation and its importance for protein targeting and function have led to the development of recombinant enzyme-replacement regimens for a number of human lysosomal storage diseases. The latest addition to this group is mucopolysaccharidosis II or Hunter syndrome. Purified human recombinant idursulfase has been shown to alter disease manifestations in individuals with Hunter syndrome. The recent approval in the US, Europe, Canada and Japan of idursulfase for the treatment of Hunter syndrome introduces the first pharmacologic agent and indeed the first specific treatment directed towards this devastating genetic disease.

摘要

重组人蛋白正被用于治疗越来越多的疾病。重组蛋白大规模生产技术的进步以及对糖基化及其在蛋白质靶向和功能方面重要性的认识,促使了针对多种人类溶酶体贮积病的重组酶替代疗法的发展。这一疗法中的最新成员是黏多糖贮积症II型,即亨特综合征。纯化的重组人艾杜糖硫酸酯酶已被证明可改变亨特综合征患者的疾病表现。最近,艾杜糖硫酸酯酶在美国、欧洲、加拿大和日本被批准用于治疗亨特综合征,这引入了第一种针对这种毁灭性遗传病的药物,也是第一种特异性治疗方法。

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