Grodeland Gunnveig, Fredriksen Agnete Brunsvik, Løset Geir Åge, Vikse Elisabeth, Fugger Lars, Bogen Bjarne
K.G. Jebsen Center for Influenza Vaccine Research, Institute of Clinical Medicine, University of Oslo and Oslo University Hospital, 0027 Oslo, Norway;
Vaccibody AS, 0349 Oslo, Norway.
J Immunol. 2016 Nov 1;197(9):3575-3585. doi: 10.4049/jimmunol.1600893. Epub 2016 Sep 26.
It has been difficult to translate promising results from DNA vaccination in mice to larger animals and humans. Previously, DNA vaccines encoding proteins that target Ag to MHC class II (MHC-II) molecules on APCs have been shown to induce rapid, enhanced, and long-lasting Ag-specific Ab titers in mice. In this study, we describe two novel DNA vaccines that as proteins target HLA class II (HLA-II) molecules. These vaccine proteins cross-react with MHC-II molecules in several species of larger mammals. When tested in ferrets and pigs, a single DNA delivery with low doses of the HLA-II-targeted vaccines resulted in rapid and increased Ab responses. Importantly, painless intradermal jet delivery of DNA was as effective as delivery by needle injection followed by electroporation. As an indication that the vaccines could also be useful for human application, HLA-II-targeted vaccine proteins were found to increase human CD4 T cell responses by a factor of ×10 in vitro. Thus, targeting of Ag to MHC-II molecules may represent an attractive strategy for increasing efficacy of DNA vaccines in larger animals and humans.
将DNA疫苗在小鼠身上取得的有前景的结果转化到更大的动物和人类身上一直存在困难。此前,编码将抗原靶向抗原呈递细胞(APC)上的MHC II类(MHC-II)分子的蛋白质的DNA疫苗已被证明能在小鼠体内诱导快速、增强且持久的抗原特异性抗体滴度。在本研究中,我们描述了两种新型DNA疫苗,其作为蛋白质靶向人类白细胞抗原II类(HLA-II)分子。这些疫苗蛋白能与几种大型哺乳动物物种中的MHC-II分子发生交叉反应。在雪貂和猪身上进行测试时,低剂量的靶向HLA-II的疫苗单次DNA递送导致抗体反应迅速增强。重要的是,DNA的无痛皮内喷射递送与通过针头注射后进行电穿孔的递送效果一样好。作为疫苗也可用于人类应用的一个迹象,发现靶向HLA-II的疫苗蛋白在体外可使人类CD4 T细胞反应增强10倍。因此,将抗原靶向MHC-II分子可能是提高DNA疫苗在大型动物和人类中疗效的一种有吸引力的策略。