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作为再生医学的眼部基因治疗?来自RPE65基因治疗莱伯先天性黑蒙的经验教训。

Gene therapy for eye as regenerative medicine? Lessons from RPE65 gene therapy for Leber's Congenital Amaurosis.

作者信息

Rakoczy Elizabeth P, Narfström Kristina

机构信息

Centre for Ophthalmology and Visual Sciences, The University of Western Australia, Crawley, 6009, Western Australia, Australia.

College of Veterinary Medicine, University of Missouri, Columbia, MO, USA.

出版信息

Int J Biochem Cell Biol. 2014 Nov;56:153-7. doi: 10.1016/j.biocel.2014.09.022. Epub 2014 Oct 5.

Abstract

Recombinant virus mediated gene therapy of Leber's Congenital Amaurosis has provided a wide range of data on the utility of gene replacement therapy for recessive diseases. Studies to date demonstrate that gene therapy in the eye is safe and can result in long-term recovery of visual function, but they also highlight that further research is required to identify optimum intervention time-points, target populations and the compatibility of associate therapies. This article is part of a directed issue entitled: Regenerative Medicine: the challenge of translation.

摘要

重组病毒介导的莱伯先天性黑蒙基因治疗已提供了大量关于基因替代疗法治疗隐性疾病效用的数据。迄今为止的研究表明,眼部基因治疗是安全的,并且可导致视觉功能的长期恢复,但这些研究也强调,需要进一步开展研究以确定最佳干预时间点、目标人群以及联合疗法的兼容性。本文是名为《再生医学:转化的挑战》的定向专题文章的一部分。

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