Moreno Fiona, Lip Florence, Rojas Hugo
uniQure biopharma B.V., Department of Research and Development, 1105 BP Amsterdam, the Netherlands.
Mol Ther Methods Clin Dev. 2022 Oct 28;27:391-403. doi: 10.1016/j.omtm.2022.10.015. eCollection 2022 Dec 8.
The insect cell-based baculovirus expression vector (BEV) system is a leading platform for scalable production of adeno-associated viruses (AAVs). The previously described One-Bac system consists of an insect packaging cell line harboring the AAV and genes and a BEV carrying the transgene and AAV inverted terminal repeats. Here we describe a new system where we successfully translated the molecular design of a double AAV expression cassette to inducible plasmid vectors. These optimized plasmid vectors employ non-canonical late promoters and alternative start codons that alleviate promoter-promoter competition. Because too much expression can be toxic to the host cells, tighter regulation of AAV expression is warranted. This has been achieved by adopting alternate baculovirus homologous region enhancers. Inoculation of the resultant stable insect packaging cell line by a recombinant BEV produced high-titer recombinant AAV (rAAV) preparations (1 × 10 genome copies/mL). Sequential batch reactor experiments indicate that this system is amenable to large-scale AAV production. We generated an insect packaging cell line that employs an optimized gene control system, ensuring stable and appropriate Rep expression. This platform produces potent and high-yield AAV particles and demonstrates potential for scale up.
基于昆虫细胞的杆状病毒表达载体(BEV)系统是用于可扩展生产腺相关病毒(AAV)的领先平台。先前描述的One-Bac系统由一个携带AAV和基因的昆虫包装细胞系以及一个携带转基因和AAV反向末端重复序列的BEV组成。在此,我们描述了一种新系统,我们成功地将双AAV表达盒的分子设计转化为可诱导质粒载体。这些优化的质粒载体采用非经典晚期启动子和替代起始密码子,以减轻启动子-启动子竞争。由于过多的表达可能对宿主细胞有毒,因此需要对AAV表达进行更严格的调控。这是通过采用替代杆状病毒同源区域增强子来实现的。用重组BEV接种所得的稳定昆虫包装细胞系可产生高滴度的重组AAV(rAAV)制剂(1×10基因组拷贝/毫升)。连续分批反应器实验表明,该系统适合大规模生产AAV。我们构建了一个采用优化的基因控制系统的昆虫包装细胞系,确保Rep的稳定和适当表达。该平台可生产高效且高产的AAV颗粒,并显示出扩大规模的潜力。