Xie Liangzhi, Metallo Christian, Warren James, Pilbrough Warren, Peltier Joseph, Zhong Tanya, Pikus Lana, Yancy Amanda, Leung John, Auniņs John G, Zhou Weichang
Fermentation and Cell Culture, Bioprocess R & D, Merck Research Laboratories, Merck & Co., Inc., West Point, Pennsylvania 19486, USA.
Biotechnol Bioeng. 2003 Jul 5;83(1):45-52. doi: 10.1002/bit.10644.
Large-scale propagation of replication-defective adenovirus vectors has not been well studied to date. One of the challenges for efficient propagation at large scale is to overcome the sensitivity of virus infected cells to gas sparging required for oxygenation and CO(2) removal. In our initial experiments, it was observed that productivity of an adenovirus vector was significantly reduced under sparging conditions as compared to nonsparged, i.e., surface-aerated controls in serum-free cultures. Investigations led to the identification of a buffer containing surfactant (Polysorbate-80, PS-80) that was included in the virus seed stock formulation and introduced through virus infection into the culture at a very low concentration as the cause of the reduced virus productivity. This finding was not obvious and trivial, as neither uninfected sparged nor infected nonsparged PER.C6 trade mark cells in serum-free cultures were affected by the buffer at such a low PS-80 concentration of 0.00025% (v/v), which is a common component of serum-free cell culture media. These results strongly suggest that virus-infected cells behave very differently from uninfected cells under sparging conditions. To mitigate the deleterious effects of sparging, the virus seed stock was prepared in the absence of the buffer containing PS-80. At the same time, the concentration of Pluronic-F68 (PF-68) in the serum-free medium was increased to 1 g/L, at which cell growth and metabolism were unaffected, even though this measure alone did not result in virus productivity improvement. Only by implementing the two measures together was virus productivity loss completely eliminated under sparging conditions. After demonstration of the process robustness in 2-L bioreactors, this adenovirus propagation process was successfully scaled up to 250 L in a 300-L bioreactor under the worst-case sparging conditions projected for 10,000-L scale.
迄今为止,复制缺陷型腺病毒载体的大规模繁殖尚未得到充分研究。大规模高效繁殖面临的挑战之一是克服病毒感染细胞对通气所需气体鼓泡的敏感性,通气用于氧合和去除二氧化碳。在我们最初的实验中,观察到与无鼓泡(即无血清培养中的表面曝气对照)相比,腺病毒载体在鼓泡条件下的生产力显著降低。研究发现,病毒种子库配方中含有的一种含有表面活性剂(聚山梨酯-80,PS-80)的缓冲液,以极低浓度通过病毒感染引入培养物中,是病毒生产力降低的原因。这一发现并非显而易见且无关紧要,因为在无血清培养中,未感染的鼓泡细胞和感染的无鼓泡PER.C6商标细胞在0.00025%(v/v)的低PS-80浓度下均不受该缓冲液影响,而这是无血清细胞培养基的常见成分。这些结果强烈表明,在鼓泡条件下,病毒感染细胞的行为与未感染细胞有很大不同。为减轻鼓泡的有害影响,在制备病毒种子库时不使用含有PS-80的缓冲液。同时,将无血清培养基中普朗尼克-F68(PF-68)的浓度提高到1 g/L,在此浓度下细胞生长和代谢不受影响,尽管仅这一措施并未提高病毒生产力。只有同时实施这两项措施,才能在鼓泡条件下完全消除病毒生产力损失。在2-L生物反应器中证明该工艺的稳健性后,在针对10000-L规模预测的最坏情况鼓泡条件下,该腺病毒繁殖工艺成功扩大到300-L生物反应器中的250 L。