摘要
慢性病毒是基因投递强大的工具,被广泛用于复制和静止状态细胞中基因功能的剖析。近来,慢性病毒也被用于基因疗法中的投递目标序列。尽管慢性病毒系统提供持续的外源基因表达,但由于其有害的插入介导诱变效应从而导致一些非目标基因沉默或激活,引发了严重的担忧。因此,大量的修饰原始的载体可能降低风险。在这里,我们简要回顾整合酶蛋白的结构,这是一个必需蛋白质用于病毒嵌入和整合;整合酶介导整合的机制;对整合酶修饰的影响。此外,我们讨论了整合酶的修饰具有的优势和未来的应用。综上所述,整合酶缺失的慢性病毒的出现不仅为我们提供了一个机会减少病毒介导插入的风险,这将提高基因治疗的安全性,而且也有利于基因修正和疫苗开发。
关键词: 基因投递,基因治疗,基因操控,整合酶缺失的慢性病毒,非整合的慢性病毒载体
Current Gene Therapy
Title:Integrase-Deficient Lentivirus: Opportunities and Challenges for Human Gene Therapy
Volume: 14 Issue: 5
Author(s): Kuan-Can Liu, Bao-Shun Lin, An-Ding Gao, Hong-Yu Ma, Meng Zhao, Rui Zhang, Hui-Hui Yan, Xun-Fei Yi, Si-Jie Lin, Jian-Wen Que and Xiao-Peng Lan
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关键词: 基因投递,基因治疗,基因操控,整合酶缺失的慢性病毒,非整合的慢性病毒载体
摘要: Lentiviruses are powerful tools for gene delivery and have been widely used for the dissection of gene functions in both replicating and quiescent cells. Recently, lentiviruses have also been used for delivering target sequences in gene therapy. Although the lentiviral system provides sustained exogenous gene expression, serious concerns have been raised due to its unfavorable insertion-mediated mutagenesis effect, thereby resulting in the silencing or activation of some unexpected genes. Thus, an array of modifications of the original vectors may reduce risks. Here, we briefly review the structure of the integrase protein, which is an essential protein for viral insertion and integration; the mechanisms of integrase-mediated integration; and the effects of the modifications of integrase. Moreover, we discuss the advantages resulting from integrase modifications and their future applications. Taken together, the generation of integrase-deficient lentivirus (IDLV) not only provides us with an opportunity to reduce the risk of virus-mediated insertions, which would improve the safety of gene therapy, but also favors gene correction and vaccine development.
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Liu Kuan-Can, Lin Bao-Shun, Gao An-Ding, Ma Hong-Yu, Zhao Meng, Zhang Rui, Yan Hui-Hui, Yi Xun-Fei, Lin Si-Jie, Que Jian-Wen and Lan Xiao-Peng, Integrase-Deficient Lentivirus: Opportunities and Challenges for Human Gene Therapy, Current Gene Therapy 2014; 14 (5) . https://dx.doi.org/10.2174/1566523214666140825124311
DOI https://dx.doi.org/10.2174/1566523214666140825124311 |
Print ISSN 1566-5232 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5631 |
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