Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
J Virol. 2019 Jan 4;93(2). doi: 10.1128/JVI.01673-18. Print 2019 Jan 15.
The influenza B virus hemagglutinin contains four major antigenic sites (the 120 loop, the 150 loop, the 160 loop, and the 190 helix) within the head domain. These immunodominant antigenic sites are the main targets of neutralizing antibodies and are subject to antigenic drift. Yet little is known about the specific antibody responses toward each site in terms of antibody prevalence and hemagglutination inhibition activity. In this study, we used modified hemagglutinins of influenza B virus which display only one or none of the major antigenic sites to measure antibody responses toward the classical as well as the noncanonical epitopes in mice, ferrets, and humans. With our novel reagents, we found that both hemagglutination inhibition antibodies and total IgGs were mostly induced by the major antigenic sites. However, in human adults, we observed high hemagglutination inhibition antibody responses toward the noncanonical epitopes. By stratifying the human samples into age groups, we found that the noncanonical antibody responses appeared to increase with age. This study dissected the specific antibody responses toward the major antigenic sites and the noncanonical epitopes of influenza B virus hemagglutinin in animals and humans using novel reagents. These findings will guide the design of the next generation of influenza virus vaccines.
乙型流感病毒血凝素的头部结构域包含四个主要抗原位点(120 环、150 环、160 环和 190 螺旋)。这些免疫显性抗原位点是中和抗体的主要靶标,易发生抗原漂移。然而,人们对每个位点的特异性抗体反应知之甚少,包括抗体流行率和血凝抑制活性。在这项研究中,我们使用了乙型流感病毒的改良血凝素,这些改良血凝素只显示一个或没有主要抗原位点,以测量小鼠、雪貂和人类对经典和非经典表位的抗体反应。使用我们的新型试剂,我们发现血凝抑制抗体和总 IgGs 主要由主要抗原位点诱导。然而,在成年人类中,我们观察到针对非经典表位的高血凝抑制抗体反应。通过将人类样本分层为年龄组,我们发现非经典抗体反应似乎随年龄增长而增加。本研究使用新型试剂在动物和人类中剖析了乙型流感病毒血凝素主要抗原位点和非经典表位的特异性抗体反应。这些发现将指导下一代流感病毒疫苗的设计。