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首页> 外文期刊>NPJ vaccines. >Heterologous prime-boost vaccination with H3N2 influenza viruses of swine favors cross-clade antibody responses and protection
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Heterologous prime-boost vaccination with H3N2 influenza viruses of swine favors cross-clade antibody responses and protection

机译:猪H3N2流感病毒异源初免-加强疫苗接种有利于交叉抗体反应和保护

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摘要

The emergence of multiple novel lineages of H1 and H3 influenza A viruses in swine has confounded control by inactivated vaccines. Because of substantial genetic and geographic heterogeneity among circulating swine influenza viruses, one vaccine strain per subtype cannot be efficacious against all of the current lineages. We have performed vaccination-challenge studies in pigs to examine whether priming and booster vaccinations with antigenically distinct H3N2 swine influenza viruses could broaden antibody responses and protection. We prepared monovalent whole inactivated, adjuvanted vaccines based on a European and a North American H3N2 swine influenza virus, which showed 81.5% aa homology in the HA1 region of the hemagglutinin and 83.4% in the neuraminidase. Our data show that (i) Priming with European and boosting with North American H3N2 swine influenza virus induces antibodies and protection against both vaccine strains, unlike prime-boost vaccination with a single virus or a single administration of bivalent vaccine. (ii) The heterologous prime-boost vaccination enhances hemagglutination inhibiting, virus neutralizing and neuraminidase inhibiting antibody responses against H3N2 viruses that are antigenically distinct from both vaccine strains. Antibody titers to the most divergent viruses were higher than after two administrations of bivalent vaccine. (iii) However, it does not induce antibodies to the conserved hemagglutinin stalk or to other hemagglutinin subtypes. We conclude that heterologous prime-boost vaccination might broaden protection to H3N2 swine influenza viruses and reduce the total amount of vaccine needed. This strategy holds potential for vaccination against influenza viruses from both humans and swine and for a better control of (reverse) zoonotic transmission of influenza viruses.
机译:猪中出现多种新型的H1和H3甲型流感病毒谱系已经使灭活疫苗的控制混乱了。由于正在循环的猪流感病毒之间存在大量的遗传和地理异质性,因此每个亚型一个疫苗株都无法有效对抗所有当前谱系。我们已经在猪中进行了疫苗接种挑战研究,以检查用抗原性不同的H3N2猪流感病毒进行的初次接种和加强接种是否可以扩大抗体反应和保护范围。我们基于欧洲和北美H3N2猪流感病毒制备了单价全灭活,佐剂疫苗,该疫苗在血凝素的HA1区显示81.5%aa同源性,在神经氨酸酶中​​显示83.4%。我们的数据显示(i)与欧洲单一疫苗和北美H3N2猪流感病毒加强疫苗可诱导抗体和针对两种疫苗株的保护,这与单一病毒或单一双价疫苗的初免加强免疫不同。 (ii)异源的初免-加强疫苗接种增强了针对H3N2病毒的血凝抑制,病毒中和和神经氨酸酶抑制的抗体应答,所述H3N2病毒在抗原上不同于两种疫苗株。对差异最大的病毒的抗体效价高于两次双价疫苗接种后的效价。 (iii)但是,它不会诱导针对保守的血凝素茎或其他血凝素亚型的抗体。我们得出结论,异源初免-加强疫苗接种可能会扩大对H3N2猪流感病毒的保护,并减少所需疫苗的总量。该策略具有针对人和猪的流感病毒进行疫苗接种以及更好地控制流感病毒(反向)人畜共患病传播的潜力。

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