Wu Chang-Jer, Lee Shan-Chih, Huang Hui-Wen, Tao Mi-Hua
Institute of Preventive Medicine, National Defense Medical Center, Taipei, Taiwan.
Vaccine. 2004 Mar 29;22(11-12):1457-64. doi: 10.1016/j.vaccine.2003.10.011.
DNA vaccines can induce protective immunity against subsequent viral challenge. However, for some DNA vaccines to be effective when administered intramuscularly, cardiotoxin pretreatment is necessary. In this study, we used the technique of in vivo electroporation to facilitate DNA delivery and elicit an immune response without the use of cardiotoxin. Intramuscular delivery of DNA (pE) encoding the Japanese encephalitis virus (JEV) envelope protein-induced anti-E antibodies only when the injected muscles were pretreated with cardiotoxin. In vivo electrotransfer of pE eliminated the need for cardiotoxin pretreatment and produced higher antibody titer than that induced by conventional intramuscular injection. Moreover, the induced immunity also conferred protection against lethal viral challenge. Interestingly, like intramuscular immunization, in vivo electroporation immunization with plasmid pE generated anti-envelope antibodies that were predominantly of the immunoglobulin G2a (IgG2a) isotype. These results suggest that in vivo electroporation can be used as an efficient gene delivery system for DNA vaccines to provide efficient protection against viral infection.
DNA疫苗可诱导针对后续病毒攻击的保护性免疫。然而,对于一些肌肉注射时有效的DNA疫苗而言,心脏毒素预处理是必要的。在本研究中,我们使用体内电穿孔技术来促进DNA递送并在不使用心脏毒素的情况下引发免疫反应。仅当注射的肌肉用心脏毒素预处理时,肌肉内递送编码日本脑炎病毒(JEV)包膜蛋白的DNA(pE)才会诱导产生抗E抗体。pE的体内电转染消除了对心脏毒素预处理的需求,并且产生的抗体滴度高于传统肌肉注射所诱导的抗体滴度。此外,诱导的免疫也赋予了针对致死性病毒攻击的保护作用。有趣的是,与肌肉内免疫一样,用质粒pE进行体内电穿孔免疫产生的抗包膜抗体主要是免疫球蛋白G2a(IgG2a)同种型。这些结果表明,体内电穿孔可用作DNA疫苗的高效基因递送系统,以提供针对病毒感染的有效保护。