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口服酵母基疫苗可提高鸡对不同禽流感 H5N1 病毒的免疫效果。

High immune efficacy against different avian influenza H5N1 viruses due to oral administration of a Saccharomyces cerevisiae-based vaccine in chickens.

机构信息

College of Medicine, Southwest Jiaotong University, Chengdu, Sichuan, China.

出版信息

Sci Rep. 2021 Apr 26;11(1):8977. doi: 10.1038/s41598-021-88413-2.

Abstract

A safe and effective vaccine is the best way to control large-scale highly pathogenic avian influenza virus (HPAI) A (H5N1) outbreaks. Saccharomyces cerevisiae (S. cerevisiae) is an ideal mucosal delivery vector for vaccine development, and we have previously shown that conventional administration of a S. cerevisiae-based vaccine (EBY100/pYD1-HA) via injection led to protection against the homologous H5N1 virus in a mouse model. Because the diameter of S. cerevisiae is approximately 10 μm, which results in a severe inflammation by injection route, therefore, oral administration is a more suitable approach for EBY100/pYD1-HA conferring protection in poultry. We extended our work by evaluating the immunogenicity and protective efficacy of oral vaccination with EBY100/pYD1-HA in the chicken model. Oral immunization with EBY100/pYD1-HA could induce robust serum IgG, mucosal IgA and cellular immune responses. Importantly, EBY100/pYD1-HA provided protection against challenges with a homologous and a heterologous H5N1 viruses. These findings suggest that EBY100/pYD1-HA, a promising H5N1 oral vaccine candidate, can avoid potential reassortment of other avian influenza viruses in oral administration of live virus vaccines and overcome the limitations of conventional injection routes. Importantly, this platform will be able to provide opportunities for broader applications in poultry during HPAI A (H5N1) outbreaks.

摘要

安全有效的疫苗是控制大规模高致病性禽流感病毒(HPAI)A(H5N1)爆发的最佳方法。酿酒酵母(Saccharomyces cerevisiae)是疫苗开发的理想黏膜递送载体,我们之前已经证明,通过注射常规给予基于酿酒酵母的疫苗(EBY100/pYD1-HA)可在小鼠模型中预防同源 H5N1 病毒。由于酿酒酵母的直径约为 10μm,通过注射途径会导致严重的炎症,因此,口服给药是 EBY100/pYD1-HA 在禽类中提供保护的更合适方法。我们通过评估在鸡模型中口服接种 EBY100/pYD1-HA 的免疫原性和保护效力来扩展我们的工作。口服免疫 EBY100/pYD1-HA 可诱导强烈的血清 IgG、黏膜 IgA 和细胞免疫反应。重要的是,EBY100/pYD1-HA 提供了针对同源和异源 H5N1 病毒的保护。这些发现表明,EBY100/pYD1-HA 作为一种有前途的 H5N1 口服疫苗候选物,可以避免活病毒疫苗口服给药时其他禽流感病毒的潜在重组,并克服传统注射途径的局限性。重要的是,该平台将能够为 HPAI A(H5N1)爆发期间在禽类中的更广泛应用提供机会。

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