Li Jingliang, Liu Guanchen, Liu Xin, Yang Jiaxin, Chang Junliang, Zhang Wenyan, Yu Xiao-Fang
First Hospital of Jilin University, Institute of Virology and AIDS Research, 130061 Changchun, China.
Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, 615 N. Wolfe Street, Baltimore, MD 21205, USA.
Viruses. 2015 Jul 17;7(7):3891-909. doi: 10.3390/v7072803.
Coxsackievirus A16 (CA16) and enterovirus 71 (EV71), both of which can cause hand, foot and mouth disease (HFMD), are responsible for large epidemics in Asian and Pacific areas. Although inactivated EV71 vaccines have completed testing in phase III clinical trials in Mainland China, CA16 vaccines are still under development. A Vero cell-based inactivated CA16 vaccine was developed by our group. Screening identified a CA16 vaccine strain (CC024) isolated from HFMD patients, which had broad cross-protective abilities and satisfied all requirements for vaccine production. Identification of the biological characteristics showed that the CA16CC024 strain had the highest titer (107.5 CCID50/mL) in Vero cells, which would benefit the development of an EV71/CA16 divalent vaccine. A potential vaccine manufacturing process was established, including the selection of optimal time for virus harvesting, membrane for diafiltration and concentration, gel-filtration chromatography for the down-stream virus purification and virus inactivation method. Altogether, the analyses suggested that the CC-16, a limiting dilution clone of the CC024 strain, with good genetic stability, high titer and broad-spectrum immunogenicity, would be the best candidate strain for a CA16 inactivated vaccine. Therefore, our study provides valuable information for the development of a Vero cell-based CA16 or EV71-CA16 divalent inactivated vaccine.
柯萨奇病毒A16型(CA16)和肠道病毒71型(EV71)均可引起手足口病(HFMD),在亚太地区引发了大规模疫情。尽管EV71灭活疫苗已在中国内地完成III期临床试验,但CA16疫苗仍在研发中。我们团队研发了一种基于Vero细胞的CA16灭活疫苗。通过筛选,从手足口病患者中分离出一种CA16疫苗株(CC024),该毒株具有广泛的交叉保护能力,满足疫苗生产的所有要求。生物学特性鉴定表明,CA16 CC024毒株在Vero细胞中的滴度最高(107.5 CCID50/mL),这将有利于EV71/CA16二价疫苗的研发。建立了一种潜在的疫苗生产工艺,包括病毒收获的最佳时间选择、渗滤和浓缩的膜、下游病毒纯化的凝胶过滤色谱法以及病毒灭活方法。总之,分析表明,CC-16作为CC024毒株的有限稀释克隆株,具有良好的遗传稳定性、高滴度和广谱免疫原性,将是CA16灭活疫苗的最佳候选毒株。因此,我们的研究为基于Vero细胞的CA16或EV71-CA16二价灭活疫苗的研发提供了有价值的信息。