Department of Cell and Molecular Biology, John A. Burns School of Medicine, University of Hawaii, Honolulu, HI, USA.
Department of Anatomy, Biochemistry and Physiology, John A. Burns School of Medicine, University of Hawaii, Honolulu, HI, USA.
Vaccine. 2014 Mar 26;32(15):1670-7. doi: 10.1016/j.vaccine.2014.01.063. Epub 2014 Feb 7.
DNA vaccination with plasmid has conventionally involved vectors designed for transient expression of antigens in injected tissues. Next generation plasmids are being developed for site-directed integration of transgenes into safe sites in host genomes and may provide an innovative approach for stable and sustained expression of antigens for vaccination. The goal of this study was to evaluate in vivo antigen expression and the generation of cell mediated immunity in mice injected with a non-integrating plasmid compared to a plasmid with integrating potential. Hyperactive piggyBac transposase-based integrating vectors (pmhyGENIE-3) contained a transgene encoding either eGFP (pmhyGENIE-3-eGFP) or luciferase (pmhyGENIE-3-GL3), and were compared to transposase-deficient plasmids with the same transgene and DNA backbone. Both non-integrating and integrating plasmids were equivalent at day 1 for protein expression at the site of injection. While protein expression from the non-integrating plasmid was lost by day 14, the pmhyGENIE-3 was found to exhibit sustained protein expression up to 28 days post-injection. Vaccination with pmhyGENIE-3-eGFP resulted in a robust CD8(+) T cell response that was three-fold higher than that of non-integrating plasmid vaccinations. Additionally we observed in splenocyte restimulation experiments that only the vaccination with pmhyGENIE-3-eGFP was characterized by IFNγ producing CD8(+) T cells. Overall, these findings suggest that plasmids designed to direct integration of transgenes into the host genome are a promising approach for designing DNA vaccines. Robust cell mediated CD8(+) T cell responses generated using integrating plasmids may provide effective, sustained protection against intracellular pathogens or tumor antigens.
DNA 疫苗接种通常涉及设计用于在注射组织中瞬时表达抗原的载体。正在开发下一代质粒,用于将转基因定点整合到宿主基因组中的安全位点,这可能为抗原的稳定和持续表达提供一种创新的疫苗接种方法。本研究的目的是评估与具有整合潜力的质粒相比,非整合质粒在注射小鼠中体内抗原表达和细胞介导免疫的产生。基于超活性 piggyBac 转座酶的整合载体(pmhyGENIE-3)包含一个编码 eGFP(pmhyGENIE-3-eGFP)或荧光素酶(pmhyGENIE-3-GL3)的转基因,与具有相同转基因和 DNA 骨架的转座酶缺陷型质粒进行比较。非整合和整合质粒在注射部位的蛋白表达方面在第 1 天是等效的。虽然非整合质粒的蛋白表达在第 14 天丢失,但发现 pmhyGENIE-3 表现出持续的蛋白表达,直到注射后 28 天。pmhyGENIE-3-eGFP 疫苗接种导致强烈的 CD8(+) T 细胞反应,比非整合质粒疫苗接种高三倍。此外,在脾细胞再刺激实验中,只有 pmhyGENIE-3-eGFP 疫苗接种的特征是 IFNγ 产生的 CD8(+) T 细胞。总体而言,这些发现表明,设计用于将转基因定向整合到宿主基因组中的质粒是设计 DNA 疫苗的一种很有前途的方法。使用整合质粒产生的强大细胞介导的 CD8(+) T 细胞反应可能为针对细胞内病原体或肿瘤抗原提供有效、持续的保护。