Rosenberg Jonathan B, Kaminsky Stephen M, Aubourg Patrick, Crystal Ronald G, Sondhi Dolan
Department of Genetic Medicine, Weill Cornell Medical College, New York, New York.
INSERM U1169, Paris, France.
J Neurosci Res. 2016 Nov;94(11):1169-79. doi: 10.1002/jnr.23792.
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.
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