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Improved poliovirus d-antigen yields by application of different Vero cell cultivation methods

机译:通过应用不同的Vero细胞培养方法提高脊髓灰质炎病毒d抗原产量

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摘要

Vero cells were grown adherent to microcarriers (Cytodex 1; 3 g L−1) using animal component free media in stirred-tank type bioreactors. Different strategies for media refreshment, daily media replacement (semi-batch), continuous media replacement (perfusion) and recirculation of media, were compared with batch cultivation. Cell densities increased using a feed strategy from 1 × 106 cells mL−1 during batch cultivation to 1.8, 2.7 and 5.0 × 106 cells mL−1 during semi-batch, perfusion and recirculation, respectively.The effects of these different cell culture strategies on subsequent poliovirus production were investigated. Increased cell densities allowed up to 3 times higher d-antigen levels when compared with that obtained from batch-wise Vero cell culture. However, the cell specific d-antigen production was lower when cells were infected at higher cell densities. This cell density effect is in good agreement with observations for different cell lines and virus types. From the evaluated alternative culture methods, application of a semi-batch mode of operations allowed the highest cell specific d-antigen production.The increased product yields that can easily be reached using these higher cell density cultivation methods, showed the possibility for better use of bioreactor capacity for the manufacturing of polio vaccines to ultimately reduce vaccine cost per dose. Further, the use of animal-component-free cell- and virus culture media shows opportunities for modernization of human viral vaccine manufacturing.
机译:使用无动物成分的培养基,在搅拌罐式生物反应器中,使Vero细胞粘附在微载体(Cytodex 1; 3 g L -1 )上。将培养基更新,每日培养基更换(半批次),连续培养基更换(灌注)和培养基再循环的不同策略与分批培养进行了比较。使用补料策略将细胞密度从分批培养期间的1×10 6 个细胞mL -1 增加到1.8、2.7和5.0×10 10个sup> 6 细胞半批量,灌注和再循环时分别为mL −1 。研究了这些不同细胞培养策略对脊髓灰质炎病毒后续生产的影响。与分批式Vero细胞培养相比,增加的细胞密度可使d抗原水平提高3倍。但是,当以较高的细胞密度感染细胞时,细胞特异性d抗原的产生较低。这种细胞密度效应与针对不同细胞系和病毒类型的观察结果非常吻合。从评估的替代培养方法来看,采用半分批操作模式可产生最高的细胞特异性d抗原。使用这些较高细胞密度的培养方法可以轻松达到更高的产品产量,这表明可以更好地利用生物反应器生产脊髓灰质炎疫苗的能力,以最终降低每剂疫苗的成本。此外,无动物成分的细胞和病毒培养基的使用显示了人类病毒疫苗生产现代化的机会。

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