Gene therapy to the kidney using viral vectors.

Paediatriki Pub Date : 2008-01-01
Talha Akbulut, Frank Park
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引用次数: 0

Abstract

Many pediatric diseases have reached a therapeutic plateau using currently available surgical and pharmacological approaches. Gene therapy has emerged as an exciting new technology to manipulate cells in the mammalian system, and in some cases, this method has achieved amazing therapeutic benefits. Compared to other organs, such as the brain, liver and lung, methods to genetically modify renal cells have received relatively little attention. The current review will discuss the challenges and important developments regarding gene therapy to the kidney, and relate the recent successes and failures to the future potential of gene therapy as a treatment modality in the context of pediatric disease.

利用病毒载体对肾脏进行基因治疗。
许多儿科疾病已经达到了目前可用的手术和药物治疗平台期。基因疗法已经成为一项令人兴奋的新技术来操纵哺乳动物系统中的细胞,在某些情况下,这种方法已经取得了惊人的治疗效果。与脑、肝和肺等其他器官相比,对肾细胞进行基因改造的方法受到的关注相对较少。当前的综述将讨论肾脏基因治疗的挑战和重要进展,并将最近的成功和失败与基因治疗作为儿科疾病治疗方式的未来潜力联系起来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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