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吡嘧司特治疗慢性 GM2 神经节苷脂病(Tay-Sachs 或桑德霍夫变异型)患者的开放标签 I/II 期临床试验。

An open-label Phase I/II clinical trial of pyrimethamine for the treatment of patients affected with chronic GM2 gangliosidosis (Tay-Sachs or Sandhoff variants).

机构信息

Research Institute, Hospital for Sick Children, Toronto, Ontario, Canada.

出版信息

Mol Genet Metab. 2011 Jan;102(1):6-12. doi: 10.1016/j.ymgme.2010.09.004. Epub 2010 Sep 17.

Abstract

Late-onset GM2 gangliosidosis is an autosomal recessive, neurodegenerative, lysosomal storage disease, caused by deficiency of ß-hexosaminidase A (Hex A), resulting from mutations in the HEXA (Tay-Sachs variant) or the HEXB (Sandhoff variant) genes. The enzyme deficiency in many patients with juvenile or adult onset forms of the disease results from the production of an unstable protein, which becomes targeted for premature degradation by the quality control system of the smooth endoplasmic reticulum and is not transported to lysosomes. In vitro studies have shown that many mutations in either the α or β subunit of Hex A can be partially rescued, i.e. enhanced levels of both enzyme protein and activity in lysosomes, following the growth of patient cells in the presence of the drug, pyrimethamine. The objectives of the present clinical trial were to establish the tolerability and efficacy of the treatment of late-onset GM2 gangliosidosis patients with escalating doses of pyrimethamine, to a maximum of 100 mg per day, administered orally in a single daily dose, over a 16-week period . The primary objective, tolerability, was assessed by regular clinical examinations, along with a panel of hematologic and biochemical studies. Although clinical efficacy could not be assessed in this short trial, treatment efficacy was evaluated by repeated measurements of leukocyte Hex A activity, expressed relative to the activity of lysosomal ß-glucuronidase. A total of 11 patients were enrolled, 8 males and 3 females, aged 23 to 50 years. One subject failed the initial screen, another was omitted from analysis because of the large number of protocol violations, and a third was withdrawn very early as a result of adverse events which were not drug-related. For the remaining 8 subjects, up to a 4-fold enhancement of Hex A activity at doses of 50 mg per day or less was observed. Additionally marked individual variations in the pharmacokinetics of the drug among the patients were noted. However, the study also found that significant side effects were experienced by most patients at or above 75 mg pyrimethamine per day. We concluded that pyrimethamine treatment enhances leukocyte Hex A activity in patients with late-onset GM2 gangliosidosis at doses lower than those associated with unacceptable side effects. Further plans are underway to extend these trials and to develop methods to assess clinical efficacy.

摘要

晚发性 GM2 神经节苷脂贮积症是一种常染色体隐性遗传、神经退行性、溶酶体贮积病,由β-己糖胺酶 A(Hex A)缺乏引起,这是由于 HEXA(Tay-Sachs 变异型)或 HEXB(桑德霍夫变异型)基因突变所致。许多青少年或成年起病形式的疾病患者的酶缺乏是由于产生不稳定的蛋白质所致,这种蛋白质成为内质网光滑区质量控制系统靶向的过早降解物,无法转运至溶酶体。体外研究表明,Hex A 的α或β亚单位的许多突变可以部分恢复,即在药物存在的情况下,患者细胞生长后,溶酶体中既增加了酶蛋白水平,又增加了酶活性。本临床试验的目的是确定递增剂量的嘧啶甲胺治疗晚发性 GM2 神经节苷脂贮积症患者的耐受性和疗效,最高剂量为每天 100mg,每日口服一次,共 16 周。主要目标是耐受性,通过定期临床检查和一系列血液学和生化学研究进行评估。尽管在这个短期试验中无法评估临床疗效,但通过白细胞 Hex A 活性的重复测量来评估治疗效果,该活性相对于溶酶体β-葡糖醛酸酶的活性进行表达。共纳入 11 例患者,男 8 例,女 3 例,年龄 23 至 50 岁。1 例患者初始筛选失败,另 1 例因违反方案规定的内容过多而被排除分析,还有 1 例患者因与药物无关的不良事件而很早就退出。对于其余 8 例患者,在每天 50mg 或更低剂量时观察到 Hex A 活性增强了 4 倍。此外,还注意到药物在患者之间的药代动力学存在明显的个体差异。然而,研究还发现,大多数患者在每天 75mg 嘧啶甲胺或更高剂量时会出现明显的副作用。我们的结论是,在低于与不可接受的副作用相关的剂量时,嘧啶甲胺治疗可增强晚发性 GM2 神经节苷脂贮积症患者的白细胞 Hex A 活性。正在计划进一步扩展这些试验并开发评估临床疗效的方法。

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