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固定床生物反应器中腺病毒载体生产的工艺开发:从实验室规模到商业规模

Process Development of Adenoviral Vector Production in Fixed Bed Bioreactor: From Bench to Commercial Scale.

作者信息

Lesch Hanna P, Heikkilä Kati M, Lipponen Eevi M, Valonen Piia, Müller Achim, Räsänen Eva, Tuunanen Tarja, Hassinen Minna M, Parker Nigel, Karhinen Minna, Shaw Robert, Ylä-Herttuala Seppo

机构信息

1 FKD Therapies, Kuopio, Finland.

2 FinVector Vision Therapies, Kuopio, Finland.

出版信息

Hum Gene Ther. 2015 Aug;26(8):560-71. doi: 10.1089/hum.2015.081.

Abstract

Large-scale vector manufacturing for phase III and beyond has proven to be challenging. Upscaling the process with suspension cells is increasingly feasible, but many viral production applications are still applicable only in adherent settings. Scaling up the adherent system has proven to be troublesome. The iCELLis(®) disposable fixed-bed bioreactors offer a possible option for viral vector manufacturing in large quantities in an adherent environment. In this study, we have optimized adenovirus serotype 5 manufacturing using iCELLis Nano with a cultivation area up to 4 m(2). HEK293 cell cultivation, infection, and harvest of the virus (by lysing the cells inside the bioreactor) proved possible, reaching total yield of up to 1.6×10(14) viral particles (vp)/batch. The iCELLis 500 is designed to satisfy demand for large-scale requirements. Inoculating a large quantity of cell mass into the iCELLis 500 was achieved by first expanding the cell mass in suspension. Upscaling the process into an iCELLis 500/100 m(2) cultivation area cassette was practical and produced up to 6.1×10(15) vp. Flask productivity per cm(2) in iCELLis Nano and iCELLis 500 was in the same range. As a conclusion, we showed for the first time that iCELLis 500 equipment has provided an effective way to manufacture large batches of adenoviral vectors.

摘要

事实证明,用于III期及后续阶段的大规模载体生产具有挑战性。扩大悬浮细胞的生产过程越来越可行,但许多病毒生产应用仍然仅适用于贴壁培养环境。事实证明,扩大贴壁系统的规模很麻烦。iCELLis(®)一次性固定床生物反应器为在贴壁环境中大量生产病毒载体提供了一种可能的选择。在本研究中,我们使用培养面积达4 m²的iCELLis Nano优化了5型腺病毒的生产。结果表明,在生物反应器内进行HEK293细胞培养、感染和病毒收获(通过裂解细胞)是可行的,每批次总产量可达1.6×10¹⁴个病毒颗粒(vp)。iCELLis 500的设计满足了大规模生产的需求。通过先在悬浮液中扩增细胞团,实现了向iCELLis 500中接种大量细胞团。将生产过程扩大到iCELLis 500/100 m²培养面积的培养盒是可行的,产量高达6.1×10¹⁵ vp。iCELLis Nano和iCELLis 500中每平方厘米培养瓶的生产力处于同一范围。总之,我们首次表明,iCELLis 500设备为大批量生产腺病毒载体提供了一种有效的方法。

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