Development of suspension adapted Vero cell culture process technology for production of viral vaccines

维罗细胞 细胞培养 生物 病毒学 悬挂(拓扑) 水泡性口炎病毒 病毒 同伦 数学 遗传学 纯数学
作者
Chun Fang Shen,Claire Guilbault,Xiuling Li,Seyyed Mehdy Elahi,Sven Ansorge,Amine Kamen,Rénald Gilbert
出处
期刊:Vaccine [Elsevier BV]
卷期号:37 (47): 6996-7002 被引量:61
标识
DOI:10.1016/j.vaccine.2019.07.003
摘要

Vero cells are considered as the most widely accepted continuous cell line by the regulatory authorities (such as WHO) for the manufacture of viral vaccines for human use. The growth of Vero cells is anchorage-dependent. Scale-up and manufacturing in adherent cultures are labor intensive and complicated. Adaptation of Vero cells to grow in suspension will simplify subcultivation and process scale-up significantly, and therefore reduce the production cost. Here we report on a successful adaptation of adherent Vero cells to grow in suspension in a serum-free and animal component-free medium (IHM03) developed in-house. The suspension adapted Vero cell cultures in IHM03 grew to similar or better maximum cell density as what was observed for the adherent Vero cells grown in commercial serum-free media and with a cell doubling time of 40-44 h. Much higher cell density (8 × 106 cells/mL) was achieved in a batch culture when three volume of the culture medium was replaced during the batch culture process. Both adherent and suspension Vero cells from various stages were tested for their authenticity using short tandem repeat analysis. Testing result indicates that all Vero cell samples had 100% concordance with the Vero DNA control sample, indicating the suspension cells maintained their genetic stability. Furthermore, suspension Vero cells at a passage number of 163 were assayed for tumorigenicity, and were not found to be tumorigenic. The viral productivity of suspension Vero cells was evaluated by using vesicular stomatitis virus (VSV) as a model. The suspension cell culture showed a better productivity of VSV than the adherent Vero cell culture. In addition, the suspension culture could be infected at higher cell densities, thus improving the volumetric virus productivity. More than one log of increase in the VSV productivity was achieved in a 3L bioreactor perfusion culture infected at a cell density of 6.8 × 106 cells/mL.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
显隐发布了新的文献求助30
1秒前
显隐发布了新的文献求助10
1秒前
显隐发布了新的文献求助10
1秒前
显隐发布了新的文献求助10
1秒前
显隐发布了新的文献求助10
1秒前
显隐发布了新的文献求助10
1秒前
显隐发布了新的文献求助10
1秒前
科研通AI5应助生生不息采纳,获得10
1秒前
显隐发布了新的文献求助10
1秒前
结实伯云发布了新的文献求助10
1秒前
听风发布了新的文献求助10
2秒前
NexusExplorer应助LLLLLLL采纳,获得10
2秒前
3秒前
卡卡西应助Sera采纳,获得20
3秒前
3秒前
标致的如雪完成签到 ,获得积分10
5秒前
跳跃隶发布了新的文献求助10
5秒前
小郭完成签到,获得积分10
7秒前
搜集达人应助王大帅采纳,获得10
7秒前
7秒前
幸福大白完成签到,获得积分10
9秒前
12秒前
春愁舟摇完成签到,获得积分10
15秒前
LLLLLLL发布了新的文献求助10
15秒前
芸苔AA完成签到,获得积分10
15秒前
斯文的小旋风举报fffffff求助涉嫌违规
15秒前
机智寻雪完成签到,获得积分10
17秒前
Hzk_发布了新的文献求助10
17秒前
啦啦啦完成签到 ,获得积分20
17秒前
英俊的铭应助刘玥言采纳,获得30
18秒前
李俊枫发布了新的文献求助10
20秒前
苏木发布了新的文献求助10
22秒前
CipherSage应助琉璃岁月采纳,获得10
22秒前
冰魂应助耶?采纳,获得10
23秒前
烟花应助qsdxasc采纳,获得10
24秒前
24秒前
25秒前
26秒前
27秒前
Hzk_完成签到,获得积分10
27秒前
高分求助中
Encyclopedia of Mathematical Physics 2nd edition 888
Introduction to Strong Mixing Conditions Volumes 1-3 500
Tip60 complex regulates eggshell formation and oviposition in the white-backed planthopper, providing effective targets for pest control 400
Optical and electric properties of monocrystalline synthetic diamond irradiated by neutrons 320
共融服務學習指南 300
Essentials of Pharmacoeconomics: Health Economics and Outcomes Research 3rd Edition. by Karen Rascati 300
Peking Blues // Liao San 300
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3801800
求助须知:如何正确求助?哪些是违规求助? 3347588
关于积分的说明 10334363
捐赠科研通 3063747
什么是DOI,文献DOI怎么找? 1682067
邀请新用户注册赠送积分活动 807893
科研通“疑难数据库(出版商)”最低求助积分说明 763960