Eliahu R, Sekeles E, Cohen R, Bach G
Am J Hum Genet. 1981 Jul;33(4):576-83.
The exogenous addition of iduronate sulfate sulfatase to cultured fibroblasts of Hunter patients resulted in a full correction of the metabolic defect as demonstrated by chemical and ultrastructural analyses. As little as 25% of the normal fibroblasts' enzyme levels were sufficient for this correction. The half-disappearance time of the internalized enzyme was 3-4 days. Prolonged incubation of corrected cells resulted in a gradual reaccumulation of mucopolysaccharides.
向亨特综合征患者的培养成纤维细胞中外源添加艾杜糖醛酸硫酸酯酶,经化学和超微结构分析表明,代谢缺陷得到了完全纠正。正常成纤维细胞酶水平低至25%就足以实现这种纠正。内化酶的半衰期为3 - 4天。对纠正后的细胞进行长时间培养会导致黏多糖逐渐重新积累。