Draz Mohamed Shehata, Wang Ying-Jie, Chen Frank Fanqing, Xu Yuhong, Shafiee Hadi
Division of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA. Faculty of Science Tanta University Tanta 31527, Egypt. State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang 310003, P. R. China.
State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang 310003, P. R. China.
Adv Funct Mater. 2017 Feb 3;27(5). doi: 10.1002/adfm.201604139. Epub 2016 Dec 14.
The promise of DNA vaccines is far-reaching. However, the development of potent immunization methods remains a key challenge for its use in clinical applications. Here, an approach for in vivo DNA vaccination by electrically activated plasmonic Au nanoparticles is reported. The electrical excitation of plasmonic nanoparticles can drive vibrational and dipole-like oscillations that are able to disrupt nearby cell membranes. In combination with their intrinsic ability to focus and magnify the electric field on the surface of cells, Au nanoparticles allow enhanced cell poration and facilitate the uptake of DNA vaccine. Mice immunized with this approach showed up to 100-fold higher gene expression compared to control treatments (without nanoparticles) and exhibited significantly increased levels of both antibody and cellular immune responses against a model hepatitis C virus DNA vaccine. This approach can be tuned to establish controlled and targeted delivery of different types of therapeutic molecules into cells and live animals as well.
DNA疫苗前景广阔。然而,开发有效的免疫方法仍是其临床应用面临的关键挑战。在此,报道了一种通过电激活等离子体金纳米颗粒进行体内DNA疫苗接种的方法。等离子体纳米颗粒的电激发可驱动振动和偶极样振荡,从而破坏附近的细胞膜。结合其在细胞表面聚焦和放大电场的固有能力,金纳米颗粒可增强细胞穿孔并促进DNA疫苗的摄取。与对照处理(无纳米颗粒)相比,用这种方法免疫的小鼠基因表达高出多达100倍,并且针对模型丙型肝炎病毒DNA疫苗的抗体和细胞免疫反应水平均显著提高。这种方法可进行调整,以实现将不同类型的治疗分子可控且靶向地递送至细胞以及活体动物体内。