Vile R G, Tuszynski A, Castleden S
Imperial Cancer Research Fund Laboratory of Cancer Gene Therapy, Rayne Institute, St Thomas' Hospital, London.
Mol Biotechnol. 1996 Apr;5(2):139-58. doi: 10.1007/BF02789062.
The majority of clinical trials for gene therapy currently employ retroviral-mediated gene delivery. This is because the life cycle of the retrovirus is well understood and can be effectively manipulated to generate vectors that can be efficiently and safely packaged. Here, we review the molecular technology behind the generation of recombinant retroviral vectors. We also highlight the problems associated with the use of these viruses as gene therapy vehicles and discuss future developments that will be necessary to maintain retroviral vectors at the forefront of gene transfer technology.
目前,大多数基因治疗临床试验采用逆转录病毒介导的基因递送。这是因为逆转录病毒的生命周期已得到充分了解,并且可以有效地进行操控以生成能够高效、安全包装的载体。在此,我们综述了重组逆转录病毒载体生成背后的分子技术。我们还强调了将这些病毒用作基因治疗载体所存在的问题,并讨论了为使逆转录病毒载体保持在基因转移技术前沿而必需的未来发展方向。