Non-Viral Vectors for Gene Delivery

Aparna Bansal and Himanshu
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引用次数: 16

Abstract

Gene therapy has emerged out as a promising therapeutic pave for the treatment of genetic and acquired diseases. Gene transfection into target cells using naked DNA is a simple and safe approach which has been further improved by combining vectors or gene carriers. Both viral and non-viral approaches have achieved a milestone to establish this technique, but non-viral approaches have attained a significant attention because of their favourable properties like less immunotoxicity and biosafety, easy to produce with versatile surface modifications, etc. Literature is rich in evidences which revealed that undoubtedly, non–viral vectors have acquired a unique place in gene therapy but still there are number of challenges which are to be overcome to increase their effectiveness and prove them ideal gene vectors. To date, tissue specific expression, long lasting gene expression system, enhanced gene transfection efficiency has been achieved with improvement in delivery methods using non-viral vectors. This review mainly summarizes the various physical and chemical methods for gene transfer in vitro and in vivo.
基因传递的非病毒载体
基因治疗已成为治疗遗传性和获得性疾病的一种有前途的治疗手段。利用裸DNA将基因转染到靶细胞中是一种简单、安全的方法,目前已通过结合载体或基因载体进一步完善。病毒和非病毒方法都取得了建立该技术的里程碑,但非病毒方法由于其免疫毒性和生物安全性较低,易于使用多种表面修饰等有利特性而获得了极大的关注。文献中丰富的证据表明,毫无疑问,非病毒载体在基因治疗中已经获得了独特的地位,但仍有许多挑战需要克服,以提高其有效性并证明它们是理想的基因载体。迄今为止,随着非病毒载体传递方法的改进,已经实现了组织特异性表达、长效基因表达系统、提高基因转染效率。本文主要综述了体外和体内基因转移的各种物理和化学方法。
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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