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血友病基因治疗:从实验室到临床的新进展。

Hemophilia Gene Therapy: New Development from Bench to Bed Side.

机构信息

Geno-immune Medical Institute, Shenzhen, China.

PKU-HKUST Shenzhen-Hong Kong Institution, Shenzhen, China.

出版信息

Curr Gene Ther. 2019;19(4):264-273. doi: 10.2174/1566523219666190924121836.

Abstract

Novel gene therapy strategies have changed the prognosis of many inherited diseases in recent years. New development in genetic tools and study models has brought us closer to a complete cure for hemophilia. This review will address the latest gene therapy research in hemophilia A and B including gene therapy tools, genetic strategies and animal models. It also summarizes the results of recent clinical trials. Potential solutions are discussed regarding the current barriers in gene therapy for hemophilia.

摘要

近年来,新型基因治疗策略改变了许多遗传性疾病的预后。基因工具和研究模型的新发展使我们更接近于实现血友病的完全治愈。本文将讨论血友病 A 和 B 的最新基因治疗研究,包括基因治疗工具、基因治疗策略和动物模型。还总结了最近临床试验的结果。本文还讨论了目前血友病基因治疗中存在的障碍的潜在解决方案。

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