Nambiar Bindu, Cornell Sookdeo Cathleen, Berthelette Patricia, Jackson Robert, Piraino Susan, Burnham Brenda, Nass Shelley, Souza David, O'Riordan Catherine R, Vincent Karen A, Cheng Seng H, Armentano Donna, Kyostio-Moore Sirkka
Sanofi , Framingham, Massachusetts.
Hum Gene Ther Methods. 2017 Feb;28(1):23-38. doi: 10.1089/hgtb.2016.124.
Several ongoing clinical studies are evaluating recombinant adeno-associated virus (rAAV) vectors as gene delivery vehicles for a variety of diseases. However, the production of vectors with genomes >4.7 kb is challenging, with vector preparations frequently containing truncated genomes. To determine whether the generation of oversized rAAVs can be improved using a producer cell-line (PCL) process, HeLaS3-cell lines harboring either a 5.1 or 5.4 kb rAAV vector genome encoding codon-optimized cDNA for human B-domain deleted Factor VIII (FVIII) were isolated. High-producing "masterwells" (MWs), defined as producing >50,000 vg/cell, were identified for each oversized vector. These MWs provided stable vector production for >20 passages. The quality and potency of the AAVrh8R/FVIII-5.1 and AAVrh8R/FVIII-5.4 vectors generated by the PCL method were then compared to those prepared via transient transfection (TXN). Southern and dot blot analyses demonstrated that both production methods resulted in packaging of heterogeneously sized genomes. However, the PCL-derived rAAV vector preparations contained some genomes >4.7 kb, whereas the majority of genomes generated by the TXN method were ≤4.7 kb. The PCL process reduced packaging of non-vector DNA for both the AAVrh8R/FVIII-5.1 and the AAVrh8R/FVIII-5.4 kb vector preparations. Furthermore, more DNA-containing viral particles were obtained for the AAVrh8R/FVIII-5.1 vector. In a mouse model of hemophilia A, animals administered a PCL-derived rAAV vector exhibited twofold higher plasma FVIII activity and increased levels of vector genomes in the liver than mice treated with vector produced via TXN did. Hence, the quality of oversized vectors prepared using the PCL method is greater than that of vectors generated using the TXN process, and importantly this improvement translates to enhanced performance in vivo.
几项正在进行的临床研究正在评估重组腺相关病毒(rAAV)载体作为多种疾病的基因递送载体。然而,生产基因组大于4.7 kb的载体具有挑战性,载体制剂中经常含有截短的基因组。为了确定使用生产细胞系(PCL)工艺是否可以改善超大rAAV的产生,分离了携带编码人B结构域缺失因子VIII(FVIII)的密码子优化cDNA的5.1或5.4 kb rAAV载体基因组的HeLaS3细胞系。对于每个超大载体,鉴定出高产的“母孔”(MW),定义为每个细胞产生>50,000 vg。这些MW提供了超过20代的稳定载体生产。然后将通过PCL方法产生的AAVrh8R/FVIII-5.1和AAVrh8R/FVIII-5.4载体的质量和效力与通过瞬时转染(TXN)制备的载体进行比较。Southern印迹和斑点印迹分析表明,两种生产方法均导致包装大小各异的基因组。然而,PCL衍生的rAAV载体制剂包含一些大于4.7 kb的基因组,而TXN方法产生的大多数基因组≤4.7 kb。PCL工艺减少了AAVrh8R/FVIII-5.1和AAVrh8R/FVIII-5.4 kb载体制剂中非载体DNA的包装。此外,对于AAVrh8R/FVIII-5.1载体获得了更多含DNA的病毒颗粒。在A型血友病小鼠模型中与用TXN产生的载体治疗的小鼠相比,给予PCL衍生的rAAV载体的动物表现出血浆FVIII活性高两倍,并且肝脏中载体基因组水平增加。因此,使用PCL方法制备的超大载体的质量大于使用TXN工艺产生的载体的质量,重要的是,这种改进转化为体内性能的增强。