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计算优化的广泛反应性抗原(COBRA)血凝素插入的重组马立克氏病病毒载体疫苗对遗传多样的 H5 高致病性禽流感病毒的效力。

Efficacy of recombinant Marek's disease virus vectored vaccines with computationally optimized broadly reactive antigen (COBRA) hemagglutinin insert against genetically diverse H5 high pathogenicity avian influenza viruses.

机构信息

Exotic and Emerging Avian Viral Diseases Research Unit, Southeast Poultry Research Laboratory, United States National Poultry Research Center, Agricultural Research Service, US Department of Agriculture, 934 College Station Rd, Athens, GA 30605, USA.

Boehringer Ingelheim Animal Health USA Inc, 1730 Olympic Drive, Athens, GA 30601, USA.

出版信息

Vaccine. 2021 Apr 1;39(14):1933-1942. doi: 10.1016/j.vaccine.2021.02.075. Epub 2021 Mar 11.

Abstract

The genetic and antigenic drift associated with the high pathogenicity avian influenza (HPAI) viruses of Goose/Guangdong (Gs/GD) lineage and the emergence of vaccine-resistant field viruses underscores the need for a broadly protective H5 influenza A vaccine. Here, we tested experimental vector herpesvirus of turkey (vHVT)-H5 vaccines containing either wild-type clade 2.3.4.4A-derived H5 inserts or computationally optimized broadly reactive antigen (COBRA) inserts with challenge by homologous and genetically divergent H5 HPAI Gs/GD lineage viruses in chickens. Direct assessment of protection was confirmed for all the tested constructs, which provided clinical protection against the homologous and heterologous H5 HPAI Gs/GD challenge viruses and significantly decreased oropharyngeal shedding titers compared to the sham vaccine. The cross reactivity was assessed by hemagglutinin inhibition (HI) and focus reduction assay against a panel of phylogenetically and antigenically diverse H5 strains. The COBRA-derived H5 inserts elicited antibody responses against antigenically diverse strains, while the wild-type-derived H5 vaccines elicited protection mostly against close antigenically related clades 2.3.4.4A and 2.3.4.4D viruses. In conclusion, the HVT vector, a widely used replicating vaccine platform in poultry, with H5 insert provides clinical protection and significant reduction of viral shedding against homologous and heterologous challenge. In addition, the COBRA-derived inserts have the potential to be used against antigenically distinct co-circulating viruses and future drift variants.

摘要

与高致病性禽流感(HPAI)鹅/广东(Gs/GD)谱系病毒相关的遗传和抗原漂移,以及疫苗抗性田间病毒的出现,突出表明需要一种广泛保护的 H5 流感 A 疫苗。在这里,我们使用同源和遗传上不同的 H5 HPAI Gs/GD 谱系病毒对含有野生型 2.3.4.4A 分支衍生 H5 插入物或计算优化的广泛反应性抗原(COBRA)插入物的实验载体火鸡疱疹病毒(vHVT)-H5 疫苗进行了测试。所有测试构建体均直接评估了保护作用,这些构建体为同源和异源 H5 HPAI Gs/GD 挑战病毒提供了临床保护,并与假疫苗相比显著降低了口咽排毒滴度。通过血凝抑制(HI)和焦点减少测定法对一组系统发育和抗原上多样化的 H5 株进行了交叉反应性评估。COBRA 衍生的 H5 插入物引起了针对抗原多样化株的抗体反应,而野生型衍生的 H5 疫苗主要引起对密切相关的抗原 2.3.4.4A 和 2.3.4.4D 病毒的保护。总之,HVT 载体,一种在禽类中广泛使用的复制疫苗平台,带有 H5 插入物,可提供针对同源和异源挑战的临床保护和显著减少病毒脱落。此外,COBRA 衍生的插入物有可能针对抗原上不同的共同循环病毒和未来的漂移变体。

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