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Measurements from normal umbilical cord blood of four lysosomal enzymatic activities: alpha-L-iduronidase (Hurler), galactocerebrosidase (globoid cell leukodystrophy), arylsulfatase A (metachromatic leukodystrophy), arylsulfatase B (Maroteaux-Lamy).

作者信息

deGasperi R, Raghavan S S, Sosa M G, Kolodny E H, Carrier C, Rubenstein P, Peters C, Wagner J, Kurtzberg J, Krivit W

机构信息

Department of Neurology, New York University School of Medicine, New York, NY, USA.

出版信息

Bone Marrow Transplant. 2000 Mar;25(5):541-4. doi: 10.1038/sj.bmt.1702185.

DOI:10.1038/sj.bmt.1702185
PMID:10713632
Abstract

Umbilical cord blood (UCB) has received increasing attention as a source of unrelated hematopoietic stem cells for transplantation. Lysosomal diseases have been effectively treated and normal enzymatic activity has occurred subsequent to engraftment using UCB. The use of donor cells with normal amounts of enzyme, rather than those from carriers whose level may be 50% or less, is an obvious goal. The frequency of such heterozygotes varies from 1:10 to 1:140 or lower depending upon the disease at issue. We assayed the levels of lysosomal enzymes in normal UCB in random samples as well as those used for transplantation. We measured the following enzymatic activities: alpha-l-iduronidase (Hurler), galactocerebrosidase (globoid cell leuko- dystrophy) and arylsulfatase A (metachromatic leukodystrophy). For the latter, levels of activity in UCB are comparable to those found in adult blood. In the case of arylsulfatase B (Maroteaux-Lamy) a level lower than adult level was found. An informed choice by the transplanting physician based on the activity of the relevant enzyme in the UCB donor will provide a better opportunity for an improved prognosis for more complete correction of the recipient's primary disease. Bone Marrow Transplantation (2000) 25, 541-544.

摘要

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Bone Marrow Transplant. 2000 Mar;25(5):541-4. doi: 10.1038/sj.bmt.1702185.
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引用本文的文献

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Blood. 2008 Oct 1;112(7):2979-89. doi: 10.1182/blood-2008-03-140830. Epub 2008 Jun 27.
2
Globoid cell leukodystrophy (Krabbe disease): normal umbilical cord blood galactocerebrosidase activity and polymorphic mutations.球状细胞脑白质营养不良症(克拉伯病):正常脐带血半乳糖脑苷脂酶活性及多态性突变
J Inherit Metab Dis. 2005;28(6):1005-9. doi: 10.1007/s10545-005-4138-z.
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Allogeneic stem cell transplantation for the treatment of lysosomal and peroxisomal metabolic diseases.
异基因干细胞移植治疗溶酶体和过氧化物酶体代谢疾病。
Springer Semin Immunopathol. 2004 Nov;26(1-2):119-32. doi: 10.1007/s00281-004-0166-2. Epub 2004 Sep 25.