Animal Health Biotechnology, Temasek Life Science Laboratory, 1 Research Link, National University of Singapore, Singapore 117604.
J Virol. 2010 Apr;84(7):3201-9. doi: 10.1128/JVI.02175-09. Epub 2010 Jan 13.
The recent outbreaks of influenza A H5N1 virus in birds and humans have necessitated the development of potent H5N1 vaccines. In this study, we evaluated the protective potential of an immediate-early promoter-based baculovirus displaying hemagglutinin (BacHA) against highly pathogenic avian influenza (HPAI) H5N1 virus infection in a mouse model. Gastrointestinal delivery of BacHA significantly enhanced the systemic immune response in terms of HA-specific serum IgG and hemagglutination inhibition (HI) titers. In addition, BacHA vaccine was able to significantly enhance the mucosal IgA level. The inclusion of recombinant cholera toxin B subunit as a mucosal adjuvant along with BacHA vaccine did not influence either the systemic or mucosal immunity. Interestingly, an inactivated form of BacHA was able to induce only a negligible level of immune responses compared to its live counterpart. Microneutralization assay also indicated that live BacHA vaccine was able to induce strong cross-clade neutralization against heterologous H5N1 strains (clade 1.0, clade 2.1, and clade 8.0) compared to the inactivated BacHA. Viral challenge studies showed that live BacHA was able to provide 100% protection against 5 50% mouse lethal doses (MLD(50)) of homologous (clade 2.1) and heterologous (clade 1) H5N1. Moreover, histopathological examinations revealed that mice vaccinated with live BacHA had only minimal bronchitis in lungs and regained their body weight more rapidly postchallenge. Furthermore, immunohistochemistry results demonstrated that the live BacHA was able to transduce and express HA in the intestinal epithelial cells in vitro and in vivo. We have demonstrated that recombinant baculovirus with a white spot syndrome virus (WSSV) immediate-early promoter 1 (ie1) acted as a vector as well as a protein vaccine and will enable the rapid production of prepandemic and pandemic vaccines without any biosafety concerns.
最近在鸟类和人类中爆发的甲型 H5N1 流感病毒,促使人们开发有效的 H5N1 疫苗。在这项研究中,我们评估了一种基于早期即刻启动子的杆状病毒展示血凝素(BacHA)在小鼠模型中对高致病性禽流感(HPAI)H5N1 病毒感染的保护潜力。BacHA 的胃肠道递送显著增强了系统免疫反应,表现为针对 HA 的血清 IgG 和血凝抑制(HI)滴度。此外,BacHA 疫苗能够显著增强黏膜 IgA 水平。将重组霍乱毒素 B 亚单位作为黏膜佐剂与 BacHA 疫苗联合使用,不会影响系统或黏膜免疫。有趣的是,与活的 BacHA 相比,灭活的 BacHA 仅能诱导可忽略不计的免疫反应。微量中和测定也表明,活的 BacHA 能够诱导针对异源 H5N1 株(1.0 谱系、2.1 谱系和 8.0 谱系)的强烈交叉谱系中和,而灭活的 BacHA 则不能。病毒攻击研究表明,活的 BacHA 能够提供 100%的保护,使其免受同源(2.1 谱系)和异源(1 谱系)H5N1 的 5 个 50%致死剂量(MLD(50))的攻击。此外,组织病理学检查显示,接种活的 BacHA 的小鼠肺部仅有轻微的支气管炎,且在攻毒后更快地恢复体重。此外,免疫组织化学结果表明,活的 BacHA 能够在体外和体内转导并表达肠上皮细胞中的 HA。我们已经证明,带有白斑综合征病毒(WSSV)早期即刻启动子 1(ie1)的重组杆状病毒不仅可以作为载体,还可以作为蛋白疫苗,在没有任何生物安全问题的情况下,能够快速生产大流行前和大流行疫苗。