Shanghai Institute of Biological Products, Shanghai 200052, China.
Virol J. 2012 Nov 23;9:286. doi: 10.1186/1743-422X-9-286.
The highly conserved nucleoprotein (NP) is an internal protein of influenza virus and is capable of inducing cross-protective immunity against different influenza A viruses, making it a main target of universal influenza vaccine. In current study, we characterized the immune response induced by DNA prime-intranasal protein boost strategy based on NP (A/PR/8/34, H1N1) in mouse model, and evaluated its protection ability against a lethal dose challenge of influenza virus.
The intranasal boost with recombinant NP (rNP) protein could effectively enhance the pre-immune response induced by the NP DNA vaccine in mice. Compared to the vaccination with NP DNA or rNP protein alone, the prime-boost strategy increased the level of NP specific serum antibody, enhanced the T cell immune response, and relatively induced more mucosal IgA antibody. The overall immune response induced by this heterologous prime-boost regimen was Th-1-biased. Furthermore, the immune response in mice induced by this strategy provided not only protection against the homologous virus but also cross-protection against a heterosubtypic H9N2 strain.
The NP DNA prime-intranasal protein boost strategy may provide an effective strategy for universal influenza vaccine development.
高度保守的核蛋白(NP)是流感病毒的内部蛋白,能够诱导针对不同甲型流感病毒的交叉保护免疫,使其成为通用流感疫苗的主要靶标。在本研究中,我们在小鼠模型中对基于 NP(A/PR/8/34,H1N1)的 DNA 初免-鼻内蛋白加强策略诱导的免疫应答进行了表征,并评估了其对致死剂量流感病毒攻击的保护能力。
用重组 NP(rNP)蛋白进行鼻内加强可有效增强 NP DNA 疫苗预先免疫诱导的反应。与单独接种 NP DNA 或 rNP 蛋白相比,初免-加强策略增加了 NP 特异性血清抗体水平,增强了 T 细胞免疫应答,并相对诱导了更多的黏膜 IgA 抗体。这种异源初免-加强方案诱导的总体免疫应答呈 Th1 偏向性。此外,该策略在小鼠中诱导的免疫应答不仅提供了针对同源病毒的保护,还提供了针对异源 H9N2 株的交叉保护。
NP DNA 初免-鼻内蛋白加强策略可能为通用流感疫苗的开发提供一种有效的策略。