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本文引用的文献

1
Viral vectors for therapy of neurologic diseases.用于治疗神经疾病的病毒载体。
Neuropharmacology. 2017 Jul 1;120:63-80. doi: 10.1016/j.neuropharm.2016.02.013. Epub 2016 Feb 21.
2
Mutation Update of ARSA and PSAP Genes Causing Metachromatic Leukodystrophy.导致异染性脑白质营养不良的ARSA和PSAP基因的突变更新
Hum Mutat. 2016 Jan;37(1):16-27. doi: 10.1002/humu.22919. Epub 2015 Nov 4.
3
Outcome of Early Juvenile Onset Metachromatic Leukodystrophy After Unrelated Cord Blood Transplantation: A Case Series and Review of the Literature.无关脐血移植后早发型幼年型异染性脑白质营养不良的结局:病例系列及文献综述
J Child Neurol. 2016 Mar;31(3):338-44. doi: 10.1177/0883073815595078. Epub 2015 Jul 17.
4
Expanded newborn screening by mass spectrometry: New tests, future perspectives.通过质谱法进行的扩大新生儿筛查:新检测方法与未来展望
Mass Spectrom Rev. 2016 Jan-Feb;35(1):71-84. doi: 10.1002/mas.21463. Epub 2015 May 7.
5
Intracerebral Gene Therapy Using AAVrh.10-hARSA Recombinant Vector to Treat Patients with Early-Onset Forms of Metachromatic Leukodystrophy: Preclinical Feasibility and Safety Assessments in Nonhuman Primates.使用AAVrh.10-hARSA重组载体进行脑内基因治疗以治疗早发型异染性脑白质营养不良患者:非人灵长类动物的临床前可行性和安全性评估
Hum Gene Ther Clin Dev. 2015 Jun;26(2):113-24. doi: 10.1089/humc.2014.139. Epub 2015 Apr 28.
6
Disease specific therapies in leukodystrophies and leukoencephalopathies.脑白质营养不良和脑白质病的疾病特异性疗法。
Mol Genet Metab. 2015 Apr;114(4):527-36. doi: 10.1016/j.ymgme.2015.01.014. Epub 2015 Feb 7.
7
A clinical approach to the diagnosis of patients with leukodystrophies and genetic leukoencephelopathies.白质营养不良和遗传性脑白质病患者的临床诊断方法
Mol Genet Metab. 2015 Apr;114(4):501-515. doi: 10.1016/j.ymgme.2014.12.434. Epub 2014 Dec 29.
8
Case definition and classification of leukodystrophies and leukoencephalopathies.脑白质营养不良和脑白质病的病例定义与分类
Mol Genet Metab. 2015 Apr;114(4):494-500. doi: 10.1016/j.ymgme.2015.01.006. Epub 2015 Jan 29.
9
The leukodystrophies.脑白质营养不良症
Semin Neurol. 2014 Jul;34(3):312-20. doi: 10.1055/s-0034-1386769. Epub 2014 Sep 5.
10
Comparative efficacy and safety of multiple routes of direct CNS administration of adeno-associated virus gene transfer vector serotype rh.10 expressing the human arylsulfatase A cDNA to nonhuman primates.将表达人芳基硫酸酯酶A cDNA的腺相关病毒基因转移载体血清型rh.10直接脑内给药的多种途径对非人灵长类动物的疗效和安全性比较
Hum Gene Ther Clin Dev. 2014 Sep;25(3):164-77. doi: 10.1089/humc.2013.239. Epub 2014 Aug 21.

用于异染性脑白质营养不良的基因治疗。

Gene therapy for metachromatic leukodystrophy.

作者信息

Rosenberg Jonathan B, Kaminsky Stephen M, Aubourg Patrick, Crystal Ronald G, Sondhi Dolan

机构信息

Department of Genetic Medicine, Weill Cornell Medical College, New York, New York.

INSERM U1169, Paris, France.

出版信息

J Neurosci Res. 2016 Nov;94(11):1169-79. doi: 10.1002/jnr.23792.

DOI:10.1002/jnr.23792
PMID:27638601
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5027970/
Abstract

Leukodystrophies (LDs) are rare, often devastating genetic disorders with neurologic symptoms. There are currently no disease-specific therapeutic approaches for these diseases. In this review we use metachromatic leukodystrophy as an example to outline in the brief the therapeutic approaches to MLD that have been tested in animal models and in clinical trials, such as enzyme-replacement therapy, bone marrow/umbilical cord blood transplants, ex vivo transplantation of genetically modified hematopoietic stem cells, and gene therapy. These studies suggest that to be successful the ideal therapy for MLD must provide persistent and high level expression of the deficient gene, arylsulfatase A in the CNS. Gene therapy using adeno-associated viruses is therefore the ideal choice for clinical development as it provides the best balance of potential for efficacy with reduced safety risk. Here we have summarized the published preclinical data from our group and from others that support the use of a gene therapy with AAVrh.10 serotype for clinical development as a treatment for MLD, and as an example of the potential of gene therapy for LDs especially for Krabbe disease, which is the focus of this special issue. © 2016 Wiley Periodicals, Inc.

摘要

脑白质营养不良(LDs)是一类罕见的、通常具有毁灭性的伴有神经症状的遗传性疾病。目前针对这些疾病尚无疾病特异性的治疗方法。在本综述中,我们以异染性脑白质营养不良为例,简要概述了在动物模型和临床试验中已得到测试的针对MLD的治疗方法,如酶替代疗法、骨髓/脐带血移植、基因改造造血干细胞的体外移植以及基因治疗。这些研究表明,要取得成功,针对MLD的理想疗法必须在中枢神经系统中持续且高水平地表达缺陷基因芳基硫酸酯酶A。因此,使用腺相关病毒的基因治疗是临床开发的理想选择,因为它在疗效潜力与降低的安全风险之间提供了最佳平衡。在此,我们总结了我们团队以及其他团队已发表的临床前数据,这些数据支持使用血清型为AAVrh.10的基因治疗进行临床开发,作为治疗MLD的方法,并且作为基因治疗对LDs尤其是对克拉伯病(本特刊的重点)潜力的一个示例。© 2016威利期刊公司