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首页> 外文期刊>Frontiers in Bioengineering and Biotechnology >Aeration and Shear Stress Are Critical Process Parameters for the Production of Oncolytic Measles Virus
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Aeration and Shear Stress Are Critical Process Parameters for the Production of Oncolytic Measles Virus

机译:曝气和剪切应力是溶瘤性麻疹病毒生产的关键过程参数

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Oncolytic Measles virus is a promising candidate for cancer treatment, but clinical studies have shown that extremely high doses (up to 1011 TCID50 per dose) are required to effect a cure. Very high titers of the virus must therefore be achieved during production to ensure an adequate supply. We have previously shown that Measles virus can be produced in Vero cells growing on a Cytodex 1 microcarrier in serum-containing medium using a stirred-tank reactor (STR). However, process optimization and further process transfer or scale up requires the identification of critical process parameters, particularly because the use of STRs increases the risk of cell damage and lower product yields due to shear stress. Using a small-scale STR (0.5 L working volume) we found that Measles virus titers are sensitive to agitator-dependent shear, with shear stress ≥0.25 N m 2 reducing the titer by more than four orders of magnitude. This effect was observed in both serum-containing and serum-free medium. At this scale, virus of titers up to 1010 TCID50 mL 1 could be achieved with an average shear stress of 0.1 N m 2. We also found that the aeration method affected the virus titer. Aeration was necessary to ensure a sufficient oxygen supply to the Vero cells, and CO2 was also needed to regulate the pH of the sodium bicarbonate buffer system. Continuous gassing with air and CO2 reduced the virus titer by four orders of magnitude compared to head-space aeration. The manufacture of oncolytic Measles virus in a STR can therefore be defined as a shear-sensitive process, but high titers can nevertheless be achieved by keeping shear stress levels below 0.25 N m 2 and by avoiding extensive gassing of the medium.
机译:溶瘤性麻疹病毒是治疗癌症的有前途的候选药物,但是临床研究表明,需要极高的剂量(每剂最高1011 TCID50)才能治愈。因此,在生产过程中必须达到很高的病毒滴度,以确保充足的供应。先前我们已经表明,使用搅拌罐反应器(STR),可以在含血清培养基中Cytodex 1微载体上生长的Vero细胞中产生麻疹病毒。但是,工艺优化以及进一步的工艺转移或规模放大需要确定关键的工艺参数,特别是因为使用STR增加了由于剪切应力而导致细胞损坏的风险并降低了产品产量。使用小规模的STR(0.5 L工作体积),我们发现麻疹病毒滴度对依赖于搅拌器的剪切敏感,剪切应力≥0.25N m 2会使滴度降低了四个数量级以上。在含血清和无血清培养基中均观察到了这种效果。在此规模下,平均剪切应力为0.1 N m 2时,可以达到最高1010 TCID50 mL 1的滴度病毒。我们还发现,通气方法会影响病毒滴度。必须通气以确保为Vero细胞提供足够的氧气,还需要CO2来调节碳酸氢钠缓冲液系统的pH。与顶空曝气相比,连续用空气和CO2充气使病毒效价降低了四个数量级。因此,可将STR中溶瘤性麻疹病毒的生产定义为对剪切敏感的过程,但仍可通过将剪切应力水平保持在0.25 N m 2以下并避免介质大量放气来实现高滴度。

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