Department of Cellular and Molecular Medicine, Glycobiology Research and Training Center, University of California San Diego, La Jolla, CA 92093, USA.
Zacharon Pharmaceuticals, Inc., San Diego, CA 92121, USA.
Mol Genet Metab. 2014 Feb;111(2):73-83. doi: 10.1016/j.ymgme.2013.07.016. Epub 2013 Jul 29.
The mucopolysaccharidoses (MPS) result from attenuation or loss of enzyme activities required for lysosomal degradation of the glycosaminoglycans, hyaluronan, heparan sulfate, chondroitin/dermatan sulfate, and keratan sulfate. This review provides a summary of glycan biomarkers that have been used to characterize animal models of MPS, for diagnosis of patients, and for monitoring therapy based on hematopoietic stem cell transplantation and enzyme replacement therapy. Recent advances have focused on the non-reducing terminus of the glycosaminoglycans that accumulate as biomarkers, using a combination of enzymatic digestion with bacterial enzymes followed by quantitative liquid chromatography/mass spectrometry. These new methods provide a simple, rapid diagnostic strategy that can be applied to samples of urine, blood, cerebrospinal fluid, cultured cells and dried blood spots from newborn infants. Analysis of the non-reducing end glycans provides a method for monitoring enzyme replacement and substrate reduction therapies and serves as a discovery tool for uncovering novel biomarkers and new forms of mucopolysaccharidoses.
黏多糖贮积症(MPS)是由于溶酶体降解糖胺聚糖、透明质酸、硫酸乙酰肝素、软骨素/硫酸皮肤素和硫酸角质素所需的酶活性减弱或丧失所致。这篇综述提供了一个总结,介绍了用于表征 MPS 动物模型、诊断患者以及基于造血干细胞移植和酶替代疗法监测治疗的聚糖生物标志物。最近的进展集中在作为生物标志物积累的糖胺聚糖的非还原末端上,使用细菌酶的酶消化组合,然后进行定量液相色谱/质谱分析。这些新方法提供了一种简单、快速的诊断策略,可应用于尿液、血液、脑脊液、培养细胞和新生儿干血斑样本。非还原末端聚糖的分析为监测酶替代和底物减少疗法提供了一种方法,并可作为发现新的生物标志物和新形式的黏多糖贮积症的发现工具。