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- W2024994505 endingPage "989" @default.
- W2024994505 startingPage "973" @default.
- W2024994505 abstract "After two decades of ups and downs, gene therapy has recently achieved a milestone in treating patients with Leber's congenital amaurosis (LCA). LCA is a group of inherited blinding diseases with retinal degeneration and severe vision loss in early infancy. Mutations in several genes, including RPE65, cause the disease. Using adenoassociated virus as a vector, three independent teams of investigators have recently shown that RPE65 can be delivered to retinal pigment epithelial cells of LCA patients by subretinal injections resulting in clinical benefits without side effects. However, considering the whole field of gene therapy, there are still major obstacles to clinical applications for other diseases. These obstacles include innate and immune barriers to vector delivery, toxicity of vectors and the lack of sustained therapeutic gene expression. Therefore, new strategies are needed to overcome these hurdles for achieving safe and effective gene therapy. In this article, we shall review the major advancements over the past two decades and, using lung gene therapy as an example, discuss the current obstacles and possible solutions to provide a roadmap for future gene therapy research." @default.
- W2024994505 created "2016-06-24" @default.
- W2024994505 creator A5081199306 @default.
- W2024994505 creator A5086356122 @default.
- W2024994505 creator A5090971530 @default.
- W2024994505 date "2011-12-01" @default.
- W2024994505 modified "2023-10-18" @default.
- W2024994505 title "Gene therapy: light is finally in the tunnel" @default.
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