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Genetic immunization by jet injection of targeted pDNA-coated nanoparticles.

机译:通过喷射注射靶向pDNA包覆的纳米粒子进行遗传免疫。

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Genetic immunization strategies have largely focused on the use of "naked" plasmid DNA or the gene gun. However, there remains a clear need to further improve the efficiency and/or cost of potential DNA vaccines. The theoretical basis of our research is to rationally design genetic immunization methodologies for nanoparticle-based delivery systems of plasmid DNA, perhaps in combination with already commercially available needle-free devices, such as the Biojector 2000. These methodologies may both reduce the dose of pDNA required and enhance the breadth and depth of protective immune responses (i.e., humoral and cellular). The purpose of this article is to provide detailed experimental methods to (1) engineer and characterize pDNA-coated cationic nanoparticles (<100nm) directly from oil-in-water microemulsion precursors and (2) enhance both the breadth and depth of immune responses after immunization of mice with pDNA-coated nanoparticles by different routes of administration, including intradermal, using a needle-free jet injection device.
机译:遗传免疫策略主要集中在“裸”质粒DNA或基因枪的使用上。但是,仍然明显需要进一步提高潜在的DNA疫苗的效率和/或成本。我们研究的理论基础是为质粒DNA的基于纳米颗粒的递送系统合理设计基因免疫方法,也许与已经商业化的无针设备(例如Biojector 2000)结合使用。这些方法都可以减少pDNA的剂量并增强保护性免疫反应(即体液和细胞)的广度和深度。本文的目的是提供详细的实验方法,以(1)直接从水包油型微乳液前体中直接工程化和表征pDNA包覆的阳离子纳米颗粒(<100nm),以及(2)增强免疫反应的广度和深度后使用无针射流注射装置通过不同的给药途径(包括皮内注射)用涂有pDNA的纳米颗粒免疫小鼠。

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