Zhang Lu, Jia Na, Li Jun, Han Yaping, Cao Wuchun, Wang Shixia, Huang Zuhu, Lu Shan
a Department of Infectious Diseases; The First Affiliated Hospital with Nanjing Medical University; Nanjing, PR China.
Hum Vaccin Immunother. 2014;10(7):1949-58. doi: 10.4161/hv.28795.
The outbreak of a novel H7N9 influenza virus in 2013 has raised serious concerns for the potential of another avian-source pandemic influenza. Effective vaccines against H7N9 virus are important in the prevention and control of any major outbreak. Novel vaccination technologies are useful additions to existing approaches. In the current report, DNA vaccine studies were conducted to identify the optimal design of an H7 HA antigen using the HA gene from a previously reported H7N7 virus that is lethal in humans as the model antigen. New Zealand White rabbits were immunized with DNA vaccines expressing 1 of 3 forms of H7 HA antigen inserts encoding the HA gene from the same H7N7 virus. High-level H7 HA-specific IgG was detected by ELISA, and functional antibodies were confirmed by hemagglutination inhibition assay and pseudotyped virus-based neutralization assay against viruses expressing HA antigens from either the previous H7N7 virus or the novel H7N9 virus. HA antigen design under the tissue plasminogen activator leader (tPA) was the most immunogenic. The data presented in the current report confirm the immunogenicity of the H7 HA antigen and provide useful guidance to prepare for an optimized H7 HA DNA vaccine to help to control the emerging H7N9 virus if and when it is needed.
2013年新型H7N9流感病毒的爆发引发了人们对另一场禽源大流行性流感潜在风险的严重担忧。有效的H7N9病毒疫苗对于预防和控制任何重大疫情至关重要。新型疫苗接种技术是现有方法的有益补充。在本报告中,开展了DNA疫苗研究,以一种先前报道的对人类致死的H7N7病毒的HA基因作为模型抗原,确定H7 HA抗原的最佳设计。用表达来自同一H7N7病毒的HA基因的3种形式的H7 HA抗原插入片段之一的DNA疫苗免疫新西兰白兔。通过ELISA检测到高水平的H7 HA特异性IgG,并通过血凝抑制试验和针对表达来自先前H7N7病毒或新型H7N9病毒的HA抗原的病毒的基于假型病毒的中和试验确认了功能性抗体。组织纤溶酶原激活剂前导序列(tPA)下的HA抗原设计免疫原性最强。本报告中的数据证实了H7 HA抗原的免疫原性,并为制备优化的H7 HA DNA疫苗提供了有用的指导,以便在需要时帮助控制新出现的H7N9病毒。