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腺相关病毒的先进生物制造与评估

Advanced biomanufacturing and evaluation of adeno-associated virus.

作者信息

Chen Kai, Kim Seulhee, Yang Siying, Varadkar Tanvi, Zhou Zhuoxin Zora, Zhang Jiashuai, Zhou Lufang, Liu Xiaoguang Margaret

机构信息

Department of Chemical and Biomolecular Engineering, The Ohio State University (OSU), 151 W Woodruff Ave, Columbus, OH, 43210, USA.

Department of Biomedical Engineering, The Ohio State University, 140 W 19th Ave, Columbus, OH, 43210, USA.

出版信息

J Biol Eng. 2024 Feb 15;18(1):15. doi: 10.1186/s13036-024-00409-4.

Abstract

Recombinant adeno-associated virus (rAAV) has been developed as a safe and effective gene delivery vehicle to treat rare genetic diseases. This study aimed to establish a novel biomanufacturing process to achieve high production and purification of various AAV serotypes (AAV2, 5, DJ, DJ8). First, a robust suspensive production process was developed and optimized using Gibco Viral Production Cell 2.0 in 30-60 mL shaker flask cultures by evaluating host cells, cell density at the time of transfection and plasmid amount, adapted to 60-100 mL spinner flask production, and scaled up to 1.2-2.0-L stirred-tank bioreactor production at 37 °C, pH 7.0, 210 rpm and DO 40%. The optimal process generated AAV titer of 7.52-8.14 × 10 vg/mL. Second, a new AAV purification using liquid chromatography was developed and optimized to reach recovery rate of 85-95% of all four serotypes. Post-purification desalting and concentration procedures were also investigated. Then the generated AAVs were evaluated in vitro using Western blotting, transmission electron microscope, confocal microscope and bioluminescence detection. Finally, the in vivo infection and functional gene expression of AAV were confirmed in tumor xenografted mouse model. In conclusion, this study reported a robust, scalable, and universal biomanufacturing platform of AAV production, clarification and purification.

摘要

重组腺相关病毒(rAAV)已被开发为一种安全有效的基因传递载体,用于治疗罕见遗传病。本研究旨在建立一种新型生物制造工艺,以实现各种AAV血清型(AAV2、5、DJ、DJ8)的高效生产和纯化。首先,通过评估宿主细胞、转染时的细胞密度和质粒量,在30 - 60 mL摇瓶培养中使用Gibco病毒生产细胞2.0开发并优化了一种稳健的悬浮生产工艺,该工艺适用于60 - 100 mL旋转瓶生产,并扩大到在37°C、pH 7.0、210 rpm和溶解氧40%的条件下进行1.2 - 2.0 L搅拌罐生物反应器生产。最佳工艺产生的AAV滴度为7.52 - 8.14×10 vg/mL。其次,开发并优化了一种使用液相色谱的新型AAV纯化方法,以使所有四种血清型的回收率达到85 - 95%。还研究了纯化后的脱盐和浓缩程序。然后使用蛋白质免疫印迹、透射电子显微镜、共聚焦显微镜和生物发光检测对产生的AAV进行体外评估。最后,在肿瘤异种移植小鼠模型中证实了AAV的体内感染和功能基因表达。总之,本研究报道了一个稳健、可扩展且通用的AAV生产、澄清和纯化生物制造平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/539e/10868095/98659439fe13/13036_2024_409_Fig1_HTML.jpg

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