Biotechnology and Applied Biochemistry · 2008 · 19 citations · 13 references
Life SciencesMolecular BiologyPathologyEnzymologyMolecular DiagnosticsMolecular PathologyBiomarkers In PathologyClinical EnzymologyEnzyme DeficienciesLysosomal Storage DisordersTherapeutic EnzymesBiomarker DetectionDermatan SulfateEnzyme Biomarkers In Disease DiagnosisEnzyme Replacement TherapyGlycosaminoglycan DegradationGlycosaminoglycan MetabolismLysosomal Storage DefectsMolecular Diagnostic Markers
MPS VI (mucopolysaccharidosis type VI) is a lysosomal storage disease in which deficient activity of the enzyme N-acetylgalactosamine 4-sulfatase [ASB (arylsulfatase B)] impairs the stepwise degradation of the GAG (glycosaminoglycan) dermatan sulfate. Clinical studies of ERT (enzyme replacement therapy) by using rhASB (recombinant human ASB) have been reported with promising results. The release of GAG into the urine is currently used as a biomarker of disease, reflecting in some cases disease severity and in all cases therapeutic responsiveness. Using RNA studies in four Italian patients undergoing ERT, we observed that TNFalpha (tumour necrosis factor alpha) might be a biomarker for MPS VI responsive to therapy. In addition to its role as a potential biomarker, TNFalpha expression could provide insights into the possible pathophysiological mechanisms underlying the mucopolysaccharidoses.
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The metabolic and molecular bases of inherited disease
Ying-Tsong Chen · Medical Entomology and Zoology · 2001 · 6.9K citations
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Enzyme replacement therapy in mucopolysaccharidosis VI (Maroteaux-Lamy syndrome)
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