Ohba Kenji, Sehara Yoshihide, Enoki Tatsuji, Mineno Junichi, Ozawa Keiya, Mizukami Hiroaki
Division of Genetic Therapeutics, Center for Molecular Medicine, Jichi Medical University, Shimotsuke, Tochigi 329-0498, Japan.
CDM Center, TAKARA Bio Inc., Kusatsu, Shiga 525-0058, Japan.
iScience. 2023 Mar 23;26(4):106487. doi: 10.1016/j.isci.2023.106487. eCollection 2023 Apr 21.
Adeno-associated virus (AAV) vectors are promising tools for gene therapy. The current AAV vector system produces an abundance of empty capsids that are eliminated before clinical use, leading to increased costs for gene therapy. In the present study, we established an AAV production system that regulates the timing of capsid expression using a tetracycline-dependent promoter. Tetracycline-regulating capsid expression increased viral yield and reduced empty capsids in various serotypes without altering AAV vector infectivity and . The replicase expression pattern change observed in the developed AAV vector system improved viral quantity and quality, whereas timing control of capsid expression reduced empty capsids. These findings provide a new perspective on the development of AAV vector production systems in gene therapy.
腺相关病毒(AAV)载体是基因治疗中很有前景的工具。当前的AAV载体系统会产生大量空衣壳,这些空衣壳在临床使用前会被清除,从而导致基因治疗成本增加。在本研究中,我们建立了一种AAV生产系统,该系统使用四环素依赖性启动子来调节衣壳表达的时间。四环素调节衣壳表达提高了各种血清型的病毒产量并减少了空衣壳,同时不改变AAV载体的感染性。在开发的AAV载体系统中观察到的复制酶表达模式变化改善了病毒的数量和质量,而衣壳表达的时间控制减少了空衣壳。这些发现为基因治疗中AAV载体生产系统的开发提供了新的视角。