Centre for Immune Regulation, Institute of Immunology, University of Oslo and Oslo University Hospital, Oslo 0027, Norway.
J Immunol. 2013 Sep 15;191(6):3221-31. doi: 10.4049/jimmunol.1300504. Epub 2013 Aug 16.
New influenza A viruses with pandemic potential periodically emerge due to viral genomic reassortment. In the face of pandemic threats, production of conventional egg-based vaccines is time consuming and of limited capacity. We have developed in this study a novel DNA vaccine in which viral hemagglutinin (HA) is bivalently targeted to MHC class II (MHC II) molecules on APCs. Following DNA vaccination, transfected cells secreted vaccine proteins that bound MHC II on APCs and initiated adaptive immune responses. A single DNA immunization induced within 8 d protective levels of strain-specific Abs and also cross-reactive T cells. During the Mexican flu pandemic, a targeted DNA vaccine (HA from A/California/07/2009) was generated within 3 wk after the HA sequences were published online. These results suggest that MHC II-targeted DNA vaccines could play a role in situations of pandemic threats. The vaccine principle should be extendable to other infectious diseases.
新型甲型流感病毒由于病毒基因组重配而具有潜在的大流行能力。面对大流行的威胁,传统的基于鸡蛋的疫苗生产既耗时又能力有限。在这项研究中,我们开发了一种新型 DNA 疫苗,其中病毒血凝素 (HA) 双价靶向 APC 上的 MHC II(MHC II)分子。在 DNA 疫苗接种后,转染的细胞分泌与 APC 上 MHC II 结合的疫苗蛋白,并引发适应性免疫反应。单次 DNA 免疫可在 8 天内诱导针对特定菌株的 Abs 和交叉反应性 T 细胞的保护性水平。在墨西哥流感大流行期间,在 HA 序列在线发布后 3 周内生成了针对 HA 的靶向 DNA 疫苗(来自 A/California/07/2009 的 HA)。这些结果表明,MHC II 靶向 DNA 疫苗可能在大流行威胁的情况下发挥作用。该疫苗原理可扩展到其他传染病。