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在初始酶替代治疗期间,MIP-1β和壳三糖苷酶呈现不同的剂量依赖性校正。

Different dose-dependent correction of MIP-1beta and chitotriosidase during initial enzyme replacement therapy.

作者信息

van Breemen M J, de Fost M, Maas M, Wiersma M G, Hollak C E M, Poll L W, Vom Dahl S, Boot R G, Aerts J M F G

机构信息

Department of Medical Biochemistry, K1-262, University of Amsterdam, Academic Medical Center, 1105 AZ, Amsterdam, The Netherlands.

出版信息

J Inherit Metab Dis. 2009 Apr;32(2):274-9. doi: 10.1007/s10545-009-1064-5. Epub 2009 Mar 4.

Abstract

In tissue lesions of type I Gaucher patients, characteristic lipid-laden macrophages, 'Gaucher cells', are surrounded by inflammatory phagocytes. Gaucher cells secrete the elevated plasma chitotriosidase. The elevated plasma MIP-1beta in Gaucher patients stems from the phagocytes surrounding the Gaucher cells. Plasma chitotriosidase and MIP-1beta decrease upon successful enzyme replacement therapy (ERT) with mannose-terminated recombinant glucocerebrosidase (alglucerase). Previous histochemical analysis of Gaucher spleens revealed that Gaucher cells express little mannose receptor, in contrast to surrounding phagocytes. We therefore investigated the corrective effects of ERT on plasma MIP-1beta and chitotriosidase in more detail. We also compared effects of one year of treatment with a relatively low dose and a relatively high dose of ERT. A more rapid correction in plasma MIP-1beta, compared to chitotriosidase, was observed in most patients on low-dose ERT. Correction of plasma MIP-1beta and chitotriosidase levels was more pronounced in the higher-dosed patient group. Upon prolonged treatment, differences in the effects of enzyme dose were no longer significant. Normalization of plasma MIP-1beta and chitotriosidase levels was attained in the majority of patients. In conclusion, ERT with mannose-terminated gluocerebrosidase results in prominent corrections of plasma chitotriosidase, a marker of Gaucher cells, and in particular of plasma MIP-1beta, a marker of inflammatory phagocytes. The sharper response in plasma MIP-1beta to ERT is in line with the observation that especially phagocytes surrounding Gaucher cells express mannose-receptors.

摘要

在I型戈谢病患者的组织病变中,特征性的富含脂质的巨噬细胞,即“戈谢细胞”,被炎性吞噬细胞所包围。戈谢细胞分泌升高的血浆壳三糖苷酶。戈谢病患者血浆中升高的MIP-1β源于围绕戈谢细胞的吞噬细胞。用甘露糖末端重组葡萄糖脑苷脂酶(阿糖苷酶)进行成功的酶替代疗法(ERT)后,血浆壳三糖苷酶和MIP-1β会降低。先前对戈谢病脾脏的组织化学分析显示,与周围的吞噬细胞相比,戈谢细胞表达很少的甘露糖受体。因此,我们更详细地研究了ERT对血浆MIP-1β和壳三糖苷酶的纠正作用。我们还比较了用相对低剂量和相对高剂量的ERT治疗一年的效果。在大多数接受低剂量ERT治疗的患者中,观察到血浆MIP-1β比壳三糖苷酶有更快的纠正。在高剂量患者组中,血浆MIP-1β和壳三糖苷酶水平的纠正更为明显。经过长期治疗,酶剂量效应的差异不再显著。大多数患者的血浆MIP-1β和壳三糖苷酶水平恢复正常。总之,用甘露糖末端葡萄糖脑苷脂酶进行ERT可显著纠正血浆壳三糖苷酶(戈谢细胞的标志物),特别是血浆MIP-1β(炎性吞噬细胞的标志物)。血浆MIP-1β对ERT的反应更明显,这与观察到的特别是围绕戈谢细胞的吞噬细胞表达甘露糖受体的现象一致。

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