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溶酶体贮积病动物模型酶替代试验中细胞和器官病理学的可逆性

Reversibility of cellular and organ pathology in enzyme replacement trials in animal models of lysosomal storage diseases.

作者信息

Gieselmann Volkmar

机构信息

Institut für Physiologische ChemieUniversität Bonn, Germany.

出版信息

Acta Paediatr Suppl. 2006 Apr;95(451):93-9. doi: 10.1111/j.1651-2227.2006.tb02397.x.

Abstract

UNLABELLED

Enzyme replacement therapy (ERT) has now become a feasible treatment option for several lysosomal storage diseases (LSDs). Although the rationale behind this approach is straightforward, there are many factors that may influence the efficacy of treatment. The reversibility of cellular and organ pathology depends on several factors including the particular organ targeted, the dose and biodistribution of enzyme, the accessibility of the target cell to the infused enzyme, the abundance of receptors for mannose-6-phosphate and other ligands in the target tissue and the activity of endocytosis. In addition, each lysosomal enzyme is unique and its ability to reverse pathology must be individually determined according to source, glycosylation and phosphorylation status. The extent to which cellular pathology may be corrected depends upon the delivery of sufficient enzyme to the diseased tissues.

CONCLUSION

Studies in animal models have identified numerous factors that influence the therapeutic efficacy of ERT. This would suggest that in patients affected by LSDs rigorous evaluation of each therapeutic preparation will be needed.

摘要

未标注

酶替代疗法(ERT)现已成为多种溶酶体贮积症(LSD)的一种可行治疗选择。尽管这种方法背后的基本原理很简单,但有许多因素可能会影响治疗效果。细胞和器官病理的可逆性取决于多个因素,包括靶向的特定器官、酶的剂量和生物分布、靶细胞对注入酶的可及性、靶组织中甘露糖 - 6 - 磷酸和其他配体受体的丰度以及内吞作用的活性。此外,每种溶酶体酶都是独特的,其逆转病理的能力必须根据来源、糖基化和磷酸化状态单独确定。细胞病理可被纠正的程度取决于向患病组织输送足够的酶。

结论

动物模型研究已经确定了许多影响ERT治疗效果的因素。这表明对于受LSD影响的患者,需要对每种治疗制剂进行严格评估。

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