Goins William F, Krisky David M, Wechuck James B, Huang Shaohua, Glorioso Joseph C
Department of Molecular Genetics and Biochemistry, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Methods Mol Biol. 2008;433:97-113. doi: 10.1007/978-1-59745-237-3_6.
Virus vectors have been employed as gene transfer vehicles for various pre-clinical and clinical gene therapy applications. Replication-competent herpes simplex virus (HSV) vectors that replicate specifically in actively dividing glial tumor cells have been used in Phase I-II human trials in patients with glioblastoma multiforme (GBM), a fatal form of brain cancer. Research during the last decade on the development of HSV vectors has resulted in the engineering of recombinant vectors that are totally replication defective, non-toxic, and capable of long-term transgene expression. This chapter describes methods for the construction of recombinant genomic HSV vectors based on the HSV-1 replication-defective vector backbones, steps in their purification, and their small-scale production for use in cell culture experiments as well as studies in animals.
病毒载体已被用作基因传递工具,用于各种临床前和临床基因治疗应用。具有复制能力的单纯疱疹病毒(HSV)载体可在活跃分裂的胶质细胞瘤细胞中特异性复制,已用于多形性胶质母细胞瘤(GBM,一种致命的脑癌形式)患者的I-II期人体试验。过去十年中关于HSV载体开发的研究已导致构建出完全复制缺陷、无毒且能够长期转基因表达的重组载体。本章描述了基于HSV-1复制缺陷载体骨架构建重组基因组HSV载体的方法、其纯化步骤以及用于细胞培养实验和动物研究的小规模生产方法。