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Intramuscular immunization with a monogenic plasmid DNA tuberculosis vaccine: Enhanced immunogenicity by electroporation and co-expression of GM-CSF transgene

机译:单基因质粒DNA结核疫苗的肌内免疫:通过电穿孔和共表达GM-CSF转基因增强免疫原性

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Plasmid DNA vaccine has been widely explored for tuberculosis immunization but there is a need to develop the ways to improve its immunogenicity. In this study, we have constructed a plasmid DNA vaccine coding for Ag85A alone or for both Ag85A and GM-CSF and investigated the immune adjuvant effects of electroporation and GM-CSF co-expression, alone or in combination, on CD4 and CD8 T cell IFN-gamma responses, CTL activities and immune protection from pulmonary Mycobacterium tuberculosis challenge in a Balb/c mouse model. We have found that use of electroporation allows a single intramuscular (i.m.) DNA injection to be as effective as repeated i.m. DNA injections in activation of both Ag85A-specific CD4 and CD8 T cells. Co-expression of immune-enhancing cytokine GM-CSF by the same plasmid DNA TB vaccine could further enhance T cell activation including CTL activities on top of electroporation. With regard to immune protection from pulmonary M. tb challenge, use of electroporation also allows a single i.m. DNA injection to be as effective as repeated i.m. DNA injections. Co-expression of GM-CSF transgene also moderately enhances immune protection and such effect is more evident for systemic protection. However, GM-CSF expression has little added effect on immune protection by electroporation-aided immunization protocols. Our findings thus will help with the development of future DNA TB immunization strategies.
机译:质粒DNA疫苗已被广泛用于结核病免疫接种,但仍需要开发提高其免疫原性的方法。在这项研究中,我们已经构建了质粒DNA疫苗,该疫苗单独编码Ag85A或同时编码Ag85A和GM-CSF,并研究了电穿孔和GM-CSF共表达对CD4和CD8 T细胞的免疫佐剂效应在Balb / c小鼠模型中,IFN-γ反应,CTL活性和来自肺结核分枝杆菌攻击的免疫保护作用。我们发现电穿孔的使用允许单次肌内(i.m.)DNA注射与重复i.m.一样有效。 DNA注射可激活Ag85A特异性CD4和CD8 T细胞。通过同一质粒DNA TB疫苗共表达免疫增强细胞因子GM-CSF可以进一步增强T细胞活化,包括在电穿孔基础上的CTL活性。关于针对肺结核分枝杆菌攻击的免疫保护,电穿孔的使用也允许单次i.m。 DNA注射与重复i.m. DNA注射。 GM-CSF转基因的共表达也适度增强了免疫保护,这种作用对于全身保护更为明显。然而,通过电穿孔辅助免疫方案,GM-CSF表达对免疫保护的作用很小。因此,我们的发现将有助于未来DNA TB免疫策略的发展。

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