Pear W S, Nolan G P, Scott M L, Baltimore D
Rockefeller University, New York, NY 10021.
Proc Natl Acad Sci U S A. 1993 Sep 15;90(18):8392-6. doi: 10.1073/pnas.90.18.8392.
The generation of high-titer, helper-free retroviruses by transient transfection has been achieved by using the highly transfectable 293T cell line into which are stably introduced constructs that express retroviral packaging functions. The resulting ecotropic virus packaging cell line BOSC 23 produces infectious retrovirus at > 10(6) infectious units/ml of supernatant within 72 hr after CaPO4-mediated transfection. A stringent assay for replication-competent virus showed that no helper virus was present. The system can produce high titers of retroviral vectors expressing genes that are extremely difficult to propagate at high titer in stable producer lines. This method should facilitate and extend the use of helper-free retroviral gene transfer, as well as be useful for gene therapy.
通过瞬时转染产生高滴度、无辅助病毒的逆转录病毒,这是通过使用高度可转染的293T细胞系实现的,在该细胞系中稳定导入了表达逆转录病毒包装功能的构建体。由此产生的嗜亲性病毒包装细胞系BOSC 23在磷酸钙介导的转染后72小时内,能产生滴度大于10(6)感染单位/毫升上清液的传染性逆转录病毒。一项针对具有复制能力病毒的严格检测表明不存在辅助病毒。该系统能够产生高滴度的逆转录病毒载体,这些载体所表达的基因在稳定的生产细胞系中极难高滴度繁殖。这种方法应能促进和扩展无辅助病毒逆转录病毒基因转移的应用,并且对基因治疗也很有用。