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底物减少疗法

Substrate reduction therapy.

作者信息

Platt Frances M, Jeyakumar Mylvaganam

机构信息

Department of Pharmacology, University of Oxford, Mansfield Road, Oxford, UK.

出版信息

Acta Paediatr. 2008 Apr;97(457):88-93. doi: 10.1111/j.1651-2227.2008.00656.x.

Abstract

UNLABELLED

The therapeutic options for lysosomal storage diseases (LSDs) have expanded greatly over the past decade, although for many disorders there is still no effective treatment. Given that the majority of LSDs involve pathological changes in both the brain and peripheral tissues, effective treatment of central nervous system (CNS) and peripheral manifestations still remains a considerable technical challenge. Type 1 Gaucher disease has two approved treatment modalities - enzyme replacement therapy (ERT) and substrate reduction therapy (SRT) - which have unique, independent and potentially complementary mechanisms of action. The availability of these two therapies has greatly increased the options for the effective clinical management of type 1 Gaucher disease. ERT involves the intravenous administration of fully functional enzyme that is taken up by cells and delivered to the lysosome, where it can compensate for the underlying enzyme deficiency. SRT uses an orally available, small molecule drug that inhibits the first committed step in glycosphingolipid biosynthesis. The aim is to reduce the rate of biosynthesis of glycosphingolipids to offset the catabolic defect, restoring the balance between the rate of biosynthesis and the rate of catabolism. SRT also has the potential to treat LSDs with CNS pathology, as the drug in clinical use (miglustat, Zavesca; Actelion Pharmaceuticals Ltd, Allschwil, Switzerland) crosses the blood-brain barrier. In this review, the current status of SRT for the treatment of Gaucher disease and other LSDs will be discussed, based upon preclinical and clinical studies.

CONCLUSION

SRT is an oral alternative treatment option for patients with type 1 Gaucher disease unwilling or unable to receive ERT. With the recent reports of clinical improvement/stabilization of CNS manifestations following SRT in patients with Niemann-Pick disease type C, miglustat may also have a role to play in the management of patients with glycosphingolipid storage in the brain. Furthermore, as SRT synergises with other therapeutic modalities, it may also prove to be a key component of combination therapies in the future.

摘要

未标注

在过去十年中,溶酶体贮积症(LSDs)的治疗选择有了很大扩展,尽管对于许多疾病仍没有有效的治疗方法。鉴于大多数LSDs涉及大脑和外周组织的病理变化,有效治疗中枢神经系统(CNS)和外周表现仍然是一项相当大的技术挑战。1型戈谢病有两种已获批的治疗方式——酶替代疗法(ERT)和底物减少疗法(SRT)——它们具有独特、独立且可能互补的作用机制。这两种疗法的可用性大大增加了1型戈谢病有效临床管理的选择。ERT涉及静脉注射全功能酶,该酶被细胞摄取并输送到溶酶体,在那里它可以弥补潜在的酶缺乏。SRT使用一种口服的小分子药物,该药物抑制糖鞘脂生物合成中的第一个关键步骤。目的是降低糖鞘脂的生物合成速率,以抵消分解代谢缺陷,恢复生物合成速率与分解代谢速率之间的平衡。SRT也有治疗伴有CNS病理的LSDs的潜力,因为临床使用的药物(米格列醇,Zavesca;Actelion制药有限公司,瑞士阿尔施维尔)可穿过血脑屏障。在本综述中,将基于临床前和临床研究讨论SRT治疗戈谢病和其他LSDs的现状。

结论

SRT是不愿或无法接受ERT的1型戈谢病患者的一种口服替代治疗选择。随着最近关于C型尼曼-匹克病患者接受SRT后CNS表现临床改善/稳定的报道,米格列醇在治疗大脑中糖鞘脂贮积患者方面可能也发挥作用。此外,由于SRT与其他治疗方式协同作用,它未来可能也会被证明是联合治疗的关键组成部分。

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