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单基因疾病基因治疗研究的未来方向展望。

A look to future directions in gene therapy research for monogenic diseases.

作者信息

Porteus Matthew H, Connelly Jon P, Pruett Shondra M

出版信息

PLoS Genet. 2006 Sep 29;2(9):e133. doi: 10.1371/journal.pgen.0020133.

Abstract

The concept of gene therapy has long appealed to biomedical researchers and clinicians because it promised to treat certain diseases at their origins. In the last several years, there have been several trials in which patients have benefited from gene therapy protocols. This progress, however, has revealed important problems, including the problem of insertional oncogenesis. In this review, which focuses on monogenic diseases, we discuss the problem of insertional oncogenesis and identify areas for future research, such as developing more quantitative assays for risk and efficacy, and ways of minimizing the genotoxic effects of gene therapy protocols, which will be important if gene therapy is to fulfill its conceptual promise.

摘要

基因治疗的概念长期以来一直吸引着生物医学研究人员和临床医生,因为它有望从根源上治疗某些疾病。在过去几年里,已经进行了几项试验,患者从基因治疗方案中受益。然而,这一进展也揭示了一些重要问题,包括插入性致癌问题。在这篇专注于单基因疾病的综述中,我们讨论了插入性致癌问题,并确定了未来研究的领域,比如开发更具定量性的风险和疗效检测方法,以及将基因治疗方案的基因毒性影响降至最低的方法。如果基因治疗要实现其概念上的前景,这些方法将至关重要。

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