Dornburg R
UMDNJ Robert Wood Johnson Medical School, Department of Molecular Genetics and Microbiology, Piscataway 08854-5635, USA.
Gene Ther. 1995 Jul;2(5):301-10.
In most human gene therapy trials, the tools of gene delivery are retroviral vectors. All current vectors are derived from murine leukemia virus (MLV). Although this system is suitable for delivering a large variety of genes into different tissues, it also has its limitations and is not adequate for all potential applications of human gene therapy. Thus, attempts are underway in many laboratories to develop other gene delivery tools. Potential agents range from non-viral based gene delivery systems (eg liposomes) to other viral vectors such as those derived from adenoviruses, adeno-associated viruses, herpes simplex virus, and several other viruses. Furthermore, the development of other, non-MLV retroviral vector systems, including one derived from HIV, is in progress in several laboratories. In this article, reticuloendotheliosis viruses and their vector systems are reviewed, and their possible use in human gene therapy is discussed.
在大多数人类基因治疗试验中,基因递送工具是逆转录病毒载体。所有当前的载体都源自鼠白血病病毒(MLV)。尽管该系统适用于将多种基因递送至不同组织,但它也有其局限性,并不适用于人类基因治疗的所有潜在应用。因此,许多实验室正在尝试开发其他基因递送工具。潜在的载体从基于非病毒的基因递送系统(如脂质体)到其他病毒载体,如源自腺病毒、腺相关病毒、单纯疱疹病毒和其他几种病毒的载体。此外,其他非MLV逆转录病毒载体系统的开发,包括一种源自HIV的系统,正在几个实验室中进行。在本文中,对网状内皮增生症病毒及其载体系统进行了综述,并讨论了它们在人类基因治疗中的可能用途。