Department of Biological Engineering, Massachusetts Institute of Technology (MIT), Cambridge, Massachusetts 02139, USA.
Nat Mater. 2013 Apr;12(4):367-76. doi: 10.1038/nmat3550. Epub 2013 Jan 27.
DNA vaccines have many potential benefits but have failed to generate robust immune responses in humans. Recently, methods such as in vivo electroporation have demonstrated improved performance, but an optimal strategy for safe, reproducible, and pain-free DNA vaccination remains elusive. Here we report an approach for rapid implantation of vaccine-loaded polymer films carrying DNA, immune-stimulatory RNA, and biodegradable polycations into the immune-cell-rich epidermis, using microneedles coated with releasable polyelectrolyte multilayers. Films transferred into the skin following brief microneedle application promoted local transfection and controlled the persistence of DNA and adjuvants in the skin from days to weeks, with kinetics determined by the film composition. These 'multilayer tattoo' DNA vaccines induced immune responses against a model HIV antigen comparable to electroporation in mice, enhanced memory T-cell generation, and elicited 140-fold higher gene expression in non-human primate skin than intradermal DNA injection, indicating the potential of this strategy for enhancing DNA vaccination.
DNA 疫苗有许多潜在的好处,但未能在人类中产生强大的免疫反应。最近,电穿孔等方法已经证明了性能的提高,但安全、可重复和无痛的 DNA 疫苗接种的最佳策略仍然难以捉摸。在这里,我们报告了一种使用带有 DNA、免疫刺激性 RNA 和可生物降解聚阳离子的负载疫苗的聚合物薄膜的快速植入方法,该方法使用带有可释放聚电解质多层的涂覆微针。在短暂的微针应用后转移到皮肤中的薄膜促进了局部转染,并控制了 DNA 和佐剂在皮肤中的持续时间,动力学由薄膜组成决定。这些“多层纹身”DNA 疫苗在小鼠中诱导了针对 HIV 模型抗原的免疫反应,增强了记忆 T 细胞的产生,并在非人类灵长类动物皮肤中引起了比皮内 DNA 注射高 140 倍的基因表达,表明该策略在增强 DNA 疫苗接种方面具有潜力。