Cornetta Kenneth, Reeves Lilith, Cross Scott
Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN, USA.
Methods Mol Biol. 2008;433:17-32. doi: 10.1007/978-1-59745-237-3_2.
Retroviral vectors were the first viral vectors to enter clinical trials and continue to be attractive candidates for applications where integration of the transgene is required. While these vectors are versatile and are used widely in the research setting, large-scale production for human use poses various challenges to insure quality and high titer. Our vector production facility has produced and certified over 20 vectors for clinical use and continues to be challenged to adapt the ever-changing vector technology to a method of production that complies with Good Manufacturing Practice (GMP). We describe two manufacturing methods for producing material for Phase I/II clinical trials and suggest ways for investigators to adapt these methods for multiple applications.
逆转录病毒载体是首批进入临床试验的病毒载体,对于需要转基因整合的应用而言,它们仍然是颇具吸引力的候选载体。虽然这些载体用途广泛,在研究领域得到了广泛应用,但用于人类的大规模生产对确保质量和高滴度提出了各种挑战。我们的载体生产设施已生产并认证了20多种用于临床的载体,并且仍面临着将不断变化的载体技术调整为符合药品生产质量管理规范(GMP)的生产方法的挑战。我们描述了两种用于生产I/II期临床试验材料的制造方法,并为研究人员提出了将这些方法应用于多种用途的建议。