Qi An Wen, Guo Su Zhi, Wen Pan Ruo, Ping Yang Bao, Chao Zhang Yong, Shi Liang, Li Qing
Hualan Biological Engineering Inc.; Xinxiang, PR China; National Key laboratory of Biochemical Engineering; Institute of Process Engineering; Chinese Academy of Sciences; Beijing, PR China.
National Key laboratory of Biochemical Engineering; Institute of Process Engineering; Chinese Academy of Sciences; Beijing, PR China.
Hum Vaccin Immunother. 2014;10(3):628-39. doi: 10.4161/hv.27295. Epub 2014 Jan 8.
We evaluated the effect of a β-propiolactone (BPL)-inactivated coxsackievirus A16 (CA16) vaccine, using three immunogenicity evaluation and two animal challenge systems. A CA16 virus strain, named 419, was used as the production strain. Another CA16 strain, named 1131, was isolated and used as the challenge strain in intracerebral inoculation of neonatal mice for the calculation of median lethal dose (LD 50). In the passive and maternal antibody-protection challenge systems, all results indicated that the vaccine could protect mouse pups from lethal challenge with the CA16 virus. In the immunogenicity systems, three types of animal (mouse, rat, and cynomolgus monkey), were immunized with the 419/CA16 vaccine. The dose-effect relationship and the antibody-generation routine were described. The CA16 vaccine induced a more potent serum antibody effect in rat than in mouse. The serum antibody titer was detectable more than 63 days after the initial vaccination. We also identified tools to evaluate the effect of the BPL-inactivated CA16 vaccine.
我们使用三种免疫原性评估方法和两种动物攻毒系统,评估了一种经β-丙内酯(BPL)灭活的柯萨奇病毒A16(CA16)疫苗的效果。一株名为419的CA16病毒株用作生产毒株。另一株名为1131的CA16毒株被分离出来,并用作新生小鼠脑内接种的攻毒毒株,用于计算半数致死剂量(LD50)。在被动和母源抗体保护攻毒系统中,所有结果均表明该疫苗可保护幼鼠免受CA16病毒的致死性攻击。在免疫原性系统中,用419/CA16疫苗对三种动物(小鼠、大鼠和食蟹猴)进行免疫。描述了剂量效应关系和抗体产生规律。CA16疫苗在大鼠中诱导的血清抗体效应比在小鼠中更强。初次接种后63天以上仍可检测到血清抗体滴度。我们还确定了评估BPL灭活CA16疫苗效果的方法。