Schmeisser Falko, Vasudevan Anupama, Verma Swati, Wang Wei, Alvarado Esmeralda, Weiss Carol, Atukorale Vajini, Meseda Clement, Weir Jerry P
Division of Viral Products, Center for Biologics Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave, Silver Spring, MD 20993, United States of America.
PLoS One. 2015 Jan 28;10(1):e0117108. doi: 10.1371/journal.pone.0117108. eCollection 2015.
Identifying major antigenic and protective epitopes of the H7 hemagglutinin (HA) will be important for understanding the antibody response to vaccines developed against the novel influenza H7N9 viruses that emerged in China in 2013. To facilitate antigenic characterization of the H7N9 HA and to develop reagents for evaluation of H7N9 candidate vaccines, we generated a panel of murine monoclonal antibodies (mAbs) to the HA of A/Shanghai/2/2013 using mammalian cell-derived virus-like particles (VLP) containing the H7 HA. Neutralizing antibodies identified an HA epitope corresponding to antigenic site A on the structurally similar influenza H3 hemagglutinin. Importantly, the neutralizing antibodies protect against A/Shanghai/2/2013 challenge. This antigenic site is conserved among many H7 viruses, including strains of both Eurasian and North American lineage, and the isolated neutralizing antibodies are cross-reactive with older H7 vaccine strains. The results indicate that the identified antigenic site is a potentially important protective epitope and suggest the potential benefit of cross-reactive antibody responses to vaccination with H7 candidate vaccines.
确定H7血凝素(HA)的主要抗原表位和保护性表位,对于理解针对2013年在中国出现的新型H7N9流感病毒所研发疫苗的抗体反应至关重要。为便于对H7N9 HA进行抗原特性分析,并开发用于评估H7N9候选疫苗的试剂,我们利用含有H7 HA的哺乳动物细胞源病毒样颗粒(VLP),制备了一组针对A/Shanghai/2/2013 HA的鼠单克隆抗体(mAb)。中和抗体鉴定出一个与结构相似的流感H3血凝素上的抗原位点A相对应的HA表位。重要的是,这些中和抗体可抵御A/Shanghai/2/2013的攻击。该抗原位点在许多H7病毒中保守,包括欧亚谱系和北美谱系的毒株,并且分离出的中和抗体与较老的H7疫苗毒株具有交叉反应性。结果表明,所鉴定的抗原位点是一个潜在重要的保护性表位,并提示了对H7候选疫苗接种产生交叉反应性抗体反应的潜在益处。