Nie Yingchao, Pan Hao, Li Qingliang, Na Huimin, Figueroa Bruno, Vincent Karen
Genomic Medicine Unit CMC, Global CMC Development, Sanofi R&D, 225 2nd Avenue, Waltham, MA 02451, USA.
Mol Ther Methods Clin Dev. 2024 Nov 4;32(4):101370. doi: 10.1016/j.omtm.2024.101370. eCollection 2024 Dec 12.
Efficient manufacturing of recombinant adenovirus-associated virus (AAV) vectors is critical to the successful development of genomic medicines. We attempted to optimize AAV vector production in a producer cell line platform. In this system, helper functions required for AAV replication and production are provided via infection with a replication-competent wild-type Adenovirus. To evaluate strategies for the reduction of replication and packaging of adenovirus and to understand the interplay of recombinant AAV and the helper virus during AAV vector production, wild-type adenovirus was compared to a mutant (Ad5ts149) containing a temperature-sensitive mutation in the DNA polymerase gene. Infection of a producer cell line with Ad5ts149 at the restrictive temperature reduced recombinant AAV titer and altered the pattern of AAV protein expression. Further investigation revealed that the adenoviral late L4-22K/33K gene products regulated both AAV gene transcription and splicing of the transcripts. Furthermore, the L4-33K gene products were found to impact AAV production in both the producer cell line and transient transfection platforms. Optimization of Adenovirus L4-22K/33K expression to facilitate efficient expression and splicing of AAV transcripts therefore represents a unique opportunity to optimize AAV vector production.
高效生产重组腺相关病毒(AAV)载体对于基因组药物的成功开发至关重要。我们试图在一个生产细胞系平台上优化AAV载体的生产。在这个系统中,AAV复制和生产所需的辅助功能是通过感染具有复制能力的野生型腺病毒来提供的。为了评估减少腺病毒复制和包装的策略,并了解在AAV载体生产过程中重组AAV与辅助病毒之间的相互作用,将野生型腺病毒与在DNA聚合酶基因中含有温度敏感突变的突变体(Ad5ts149)进行了比较。在限制温度下用Ad5ts149感染生产细胞系会降低重组AAV滴度,并改变AAV蛋白表达模式。进一步研究表明,腺病毒晚期L4-22K/33K基因产物调节AAV基因转录和转录本的剪接。此外,发现L4-33K基因产物在生产细胞系和瞬时转染平台中均影响AAV的生产。因此,优化腺病毒L4-22K/33K表达以促进AAV转录本的高效表达和剪接,为优化AAV载体生产提供了一个独特的机会。