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Development of a new candidate H5N1 avian influenza virus for pre‐pandemic vaccine production

机译:开发用于大流行前疫苗生产的新型候选H5N1禽流感病毒

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摘要

>Background  Highly pathogenic H5N1 avian influenza viruses currently circulating in birds have caused hundreds of human infections, and pose a significant pandemic threat. Vaccines are a major component of the public health preparedness for this likely event. The rapid evolution of H5N1 viruses has resulted in the emergence of multiple clades with distinct antigenic characteristics that require clade‐specific vaccines. A variant H5N1 virus termed clade 2.3.4 emerged in 2005 and has caused multiple fatal infections. Vaccine candidates that match the antigenic properties of variant viruses are necessary because inactivated influenza vaccines elicit strain‐specific protection. >Objective  To address the need for a suitable seed for manufacturing a clade 2.3.4 vaccine, we developed a new H5N1 pre‐pandemic candidate vaccine by reverse genetics and evaluated its safety and replication in vitro and in vivo. >Methods  A reassortant virus termed, Anhui/PR8, was produced by reverse genetics in compliance with WHO pandemic vaccine development guidelines and contains six genes from A/Puerto Rico/8/34 as well as the neuraminidase and hemagglutinin (HA) genomic segments from the A/Anhui/01/2005 virus. The multi‐basic cleavage site of HA was removed to reduce virulence. >Results  The reassortant Anhui/PR8 grows well in eggs and is avirulent to chicken and ferrets but retains the antigenicity of the parental A/Anhui/01/2005 virus. >Conclusion  These results indicate that the Anhui/PR8 reassortant lost a major virulent determinant and it is suitable for its use in vaccine manufacturing and as a reference vaccine virus against the H5N1 clade 2.3.4 viruses circulating in eastern China, Vietnam, Thailand, and Laos.
机译:>背景当前在鸟类中传播的高致病性H5N1禽流感病毒已经造成数百种人类感染,并构成了大流行的威胁。疫苗是这一可能事件的公共卫生准备工作的重要组成部分。 H5N1病毒的快速进化导致出现了多个具有独特抗原特性的进化枝,需要进化枝特异性疫苗。 2005年出现了一种名为进化枝2.3.4的H5N1变异病毒,已引起多种致命感染。与变种病毒的抗原特性相匹配的候选疫苗是必需的,因为灭活的流感疫苗可引起菌株特异性保护。 >目的:为了满足生产2.3.4进化枝疫苗所需的合适种子的需求,我们通过反向遗传学开发了一种新的H5N1大流行前候选疫苗,并评估了其在体内外的安全性和复制性。 >方法根据世界卫生组织大流行疫苗开发指南,通过反向遗传学生产了一种名为安徽/ PR8的重配病毒,其中包含来自A / Puerto Rico / 8/34的六个基因以及神经氨酸酶和血凝素A / Anhui / 01/2005病毒的(HA)基因组片段。 HA的多碱基切割位点被去除,以降低毒力。 >结果重配的安徽/ PR8在卵中生长良好,对鸡和雪貂无毒,但保留了亲本A / Anhui / 01/2005病毒的抗原性。 >结论这些结果表明,安徽/ PR8重配子丧失了主要的毒力决定因素,适合用于疫苗生产以及作为针对中国东部流行的H5N1进化枝2.3.4病毒的参考疫苗病毒。 ,越南,泰国和老挝。

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