Kirchenbaum Greg A, Carter Donald M, Ross Ted M
Center for Vaccines and Immunology, Department of Infectious Diseases, College of Veterinary Medicine, University of Georgia, Athens, Georgia, USA; Vaccine and Gene Therapy Institute of Florida, Port Saint Lucie, Florida, USA.
Center for Vaccines and Immunology, Department of Infectious Diseases, College of Veterinary Medicine, University of Georgia, Athens, Georgia, USA; Vaccine and Gene Therapy Institute of Florida, Port Saint Lucie, Florida, USA
J Virol. 2015 Nov 11;90(2):1116-28. doi: 10.1128/JVI.02372-15. Print 2016 Jan 15.
Broadly reactive antibodies targeting the conserved hemagglutinin (HA) stalk region are elicited following sequential infection or vaccination with influenza viruses belonging to divergent subtypes and/or expressing antigenically distinct HA globular head domains. Here, we demonstrate, through the use of novel chimeric HA proteins and competitive binding assays, that sequential infection of ferrets with antigenically distinct seasonal H1N1 (sH1N1) influenza virus isolates induced an HA stalk-specific antibody response. Additionally, stalk-specific antibody titers were boosted following sequential infection with antigenically distinct sH1N1 isolates in spite of preexisting, cross-reactive, HA-specific antibody titers. Despite a decline in stalk-specific serum antibody titers, sequential sH1N1 influenza virus-infected ferrets were protected from challenge with a novel H1N1 influenza virus (A/California/07/2009), and these ferrets poorly transmitted the virus to naive contacts. Collectively, these findings indicate that HA stalk-specific antibodies are commonly elicited in ferrets following sequential infection with antigenically distinct sH1N1 influenza virus isolates lacking HA receptor-binding site cross-reactivity and can protect ferrets against a pathogenic novel H1N1 virus.
The influenza virus hemagglutinin (HA) is a major target of the humoral immune response following infection and/or seasonal vaccination. While antibodies targeting the receptor-binding pocket of HA possess strong neutralization capacities, these antibodies are largely strain specific and do not confer protection against antigenic drift variant or novel HA subtype-expressing viruses. In contrast, antibodies targeting the conserved stalk region of HA exhibit broader reactivity among viruses within and among influenza virus subtypes. Here, we show that sequential infection of ferrets with antigenically distinct seasonal H1N1 influenza viruses boosts the antibody responses directed at the HA stalk region. Moreover, ferrets possessing HA stalk-specific antibody were protected against novel H1N1 virus infection and did not transmit the virus to naive contacts.
在用属于不同亚型和/或表达抗原性不同的血凝素(HA)球状头部结构域的流感病毒进行连续感染或接种疫苗后,会引发针对保守HA茎部区域的广泛反应性抗体。在这里,我们通过使用新型嵌合HA蛋白和竞争性结合试验证明,雪貂先后感染抗原性不同的季节性H1N1(sH1N1)流感病毒分离株可诱导HA茎部特异性抗体反应。此外,尽管存在预先存在的、交叉反应性的、HA特异性抗体滴度,但在用抗原性不同的sH1N1分离株进行连续感染后,茎部特异性抗体滴度仍会升高。尽管茎部特异性血清抗体滴度有所下降,但先后感染sH1N1流感病毒的雪貂对新型H1N1流感病毒(A/California/07/2009)的攻击具有抵抗力,并且这些雪貂很少将病毒传播给未接触过病毒的接触者。总体而言,这些发现表明,在雪貂先后感染缺乏HA受体结合位点交叉反应性的抗原性不同的sH1N1流感病毒分离株后,通常会引发HA茎部特异性抗体,并且可以保护雪貂免受致病性新型H1N1病毒的侵害。
流感病毒血凝素(HA)是感染和/或季节性接种疫苗后体液免疫反应的主要靶点。虽然针对HA受体结合口袋的抗体具有强大的中和能力,但这些抗体在很大程度上是毒株特异性的,不能提供针对抗原漂移变异株或表达新型HA亚型的病毒的保护。相比之下,针对HA保守茎部区域的抗体在流感病毒亚型内和亚型间的病毒中表现出更广泛的反应性。在这里,我们表明雪貂先后感染抗原性不同的季节性H1N1流感病毒会增强针对HA茎部区域的抗体反应。此外,拥有HA茎部特异性抗体的雪貂对新型H1N1病毒感染具有抵抗力,并且不会将病毒传播给未接触过病毒的接触者。