Liu Lu, Nachbagauer Raffael, Zhu Lingyan, Huang Yang, Xie Xinci, Jin Shan, Zhang Anli, Wan Yanmin, Hirsh Ariana, Tian Di, Shi Xiaolin, Dong Zhaoguang, Yuan Songhua, Hu Yunwen, Krammer Florian, Zhang Xiaoyan, Xu Jianqing
Shanghai Public Health Clinical Center & Institutes of Biomedical Sciences, Key Laboratory of Medical Molecular Virology of Ministry of Education/Health, Shanghai Medical College, Fudan University, China.
Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, USA.
J Infect Dis. 2017 Feb 15;215(4):518-528. doi: 10.1093/infdis/jiw608.
The outbreak of novel avian H7N9 influenza virus infections in China in 2013 has demonstrated the continuing threat posed by zoonotic pathogens. Deciphering the immune response during natural infection will guide future vaccine development.
We assessed the induction of heterosubtypic cross-reactive antibodies induced by H7N9 infection against a large panel of recombinant hemagglutinins and neuraminidases by quantitative enzyme-linked immunosorbent assay, and novel chimeric hemagglutinin constructs were used to dissect the anti-stalk or -head humoral immune response.
H7N9 infection induced strong antibody responses against divergent H7 hemagglutinins. Interestingly, we also found induction of antibodies against heterosubtypic hemagglutinins from both group 1 and group 2 and a boost in heterosubtypic neutralizing activity in the absence of hemagglutination inhibitory activity. Kinetic monitoring revealed that heterosubtypic binding/neutralizing antibody responses typically appeared and peaked earlier than intrasubtypic responses, likely mediated by memory recall responses.
Our results indicate that cross-group binding and neutralizing antibody responses primarily targeting the stalk region can be elicited after natural influenza virus infection. These data support our understanding of the breadth of the postinfection immune response that could inform the design of future, broadly protective influenza virus vaccines.
2013年中国新型H7N9禽流感病毒感染的爆发已表明人畜共患病原体构成的持续威胁。解析自然感染期间的免疫反应将指导未来疫苗的开发。
我们通过定量酶联免疫吸附测定评估了H7N9感染诱导的针对大量重组血凝素和神经氨酸酶的异源亚型交叉反应抗体的诱导情况,并使用新型嵌合血凝素构建体剖析抗茎部或头部的体液免疫反应。
H7N9感染诱导了针对不同H7血凝素的强烈抗体反应。有趣的是,我们还发现诱导了针对第1组和第2组异源亚型血凝素的抗体,并且在没有血凝抑制活性的情况下异源亚型中和活性增强。动力学监测显示,异源亚型结合/中和抗体反应通常比同源亚型反应出现得更早且达到峰值,这可能由记忆回忆反应介导。
我们的结果表明,自然感染流感病毒后可引发主要针对茎部区域的跨组结合和中和抗体反应。这些数据支持我们对感染后免疫反应广度的理解,这可为未来广泛保护性流感病毒疫苗的设计提供参考。