Fu Xiaotong, Chen Wei-Chiang, Argento Christopher, Clarner Peter, Bhatt Vinay, Dickerson Ryan, Bou-Assaf George, Bakhshayeshi Meisam, Lu Xiaohui, Bergelson Svetlana, Pieracci John
1Gene Therapy, Process Development and Biogen, Cambridge, Massachusetts.
2Analytical Development, Biogen, Cambridge, Massachusetts.
Hum Gene Ther Methods. 2019 Aug;30(4):144-152. doi: 10.1089/hgtb.2019.088.
Recombinant adeno-associated virus (rAAV)-mediated gene therapy is a fast-evolving field in the biotechnology industry. One of the major challenges in developing a purification process for AAV gene therapy is establishing an effective yet scalable method to remove empty capsids, or viral vectors lacking the therapeutic gene, from full capsids-viral product containing the therapeutic sequence. Several analytical methods that can quantify the empty-to-full capsid ratio have been reported in the literature. However, as samples can vary widely in viral titer, buffer matrix, and the relative level of empty capsids, understanding the specifications and limitations of different analytical methods is critical to providing appropriate support to facilitate process development. In this study, we developed a novel anion-exchange high-performance liquid chromatography assay to determine the empty-to-full capsid ratio of rAAV samples. The newly developed method demonstrated good comparability with both the transmission electron microscopy and analytical ultracentrifugation methods used in empty-to-full capsid ratio quantification, while providing much higher assay throughput and reducing the minimum sample concentration requirement to 2.7E11 viral genomes/mL.
重组腺相关病毒(rAAV)介导的基因治疗是生物技术行业中一个快速发展的领域。开发AAV基因治疗纯化工艺的主要挑战之一是建立一种有效且可扩展的方法,从含有治疗序列的完整衣壳病毒产物中去除空衣壳,即缺乏治疗基因的病毒载体。文献中已经报道了几种能够量化空衣壳与完整衣壳比例的分析方法。然而,由于样品的病毒滴度、缓冲液基质和空衣壳的相对水平可能差异很大,了解不同分析方法的规格和局限性对于提供适当支持以促进工艺开发至关重要。在本研究中,我们开发了一种新型阴离子交换高效液相色谱法来测定rAAV样品的空衣壳与完整衣壳比例。新开发的方法在空衣壳与完整衣壳比例定量中与透射电子显微镜法和分析超速离心法均具有良好的可比性,同时提供了更高的分析通量,并将最低样品浓度要求降低至2.7E11病毒基因组/mL。