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Immobilization of 293 cells using porous support particles for adenovirus vector production

机译:使用多孔载体颗粒固定293细胞以生产腺病毒载体

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摘要

Adenovirus vector production by anchorage-independent 293 cells immobilized using porous biomass support particles (BSPs) was investigated in static and shake-flask cultures for efficient large-scale production of adenovirus vectors for gene therapy applications. The density of cells immobilized within BSPs was evaluated by measuring their WST-8 (2-(2-methoxy-4-nitrophenyl)-3-(4-nitrophenyl)-5-(2,4-disulfophenyl)-2H-tetrazolium, monosodium salt) reduction activity. In shake-flask culture, 293-F cells, which were adapted to serum-free suspension culture, were not successfully retained within reticulated polyvinyl formal (PVF) resin BSPs (2 × 2 × 2 mm cubes) with matrices of relatively small pores (pore diameter 60 μm). When the BSPs were coated with a cationic polymer polyethyleneimine, a high cell density of more than 107 cells cm−3-BSP was achieved in both static and shake-flask cultures with regular replacement of the culture medium. After infection with an adenovirus vector carrying the enhanced green fluorescent protein gene (Ad EGFP), the specific Ad EGFP productivity of the immobilized cells was comparable to the maximal productivity of non-immobilized 293-F cells by maintaining favorable conditions in the culture environment.
机译:在静态和摇瓶培养物中研究了通过使用多孔生物量支持颗粒(BSP)固定化的不依赖锚定的293细胞生产腺病毒载体的情况,以有效地大规模生产用于基因治疗的腺病毒载体。通过测量其WST-8(2-(2-甲氧基-4-硝基苯基)-3-(4-硝基苯基)-5-(2,4-二磺基苯基)-2H-四唑来评估固定在BSP中的细胞密度,单钠盐)还原活性。在摇瓶培养中,适应于无血清悬浮培养的293-F细胞未成功保留在具有相对较小孔基质的网状聚乙烯缩甲醛(PVF)树脂BSP(2×2×2 mm立方体)中孔径60μm)。当BSPs用阳离子聚合物聚乙烯亚胺包被时,在静态和摇瓶培养中都获得了超过10 7 cm -3 -BSP的高细胞密度定期更换培养基。用携带增强的绿色荧光蛋白基因(Ad EGFP)的腺病毒载体感染后,通过在培养环境中保持良好的条件,固定化细胞的比对Ad EGFP生产率可与未固定化293-F细胞的最大生产率相比。

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