Phillpotts R J, Venugopal K, Brooks T
Microbiology Group, Chemical and Biological Defence Establishment, Porton Down, Wiltshire, U.K.
Arch Virol. 1996;141(3-4):743-9. doi: 10.1007/BF01718332.
In vivo transfection by intramuscular injection with plasmids expressing the immunogenic proteins of microbial pathogens has considerable potential as a vaccination strategy against many pathogens of both man and animals. Here we report that weanling mice given a single intramuscular injection of 50 micrograms of a plasmid, pSLE1 expressing the St. Louis encephalitis virus (SLE) prM/E protein under the control of the cytomegalovirus immediate early protein promoter produced SLE-specific antibody and were protected against lethal challenge with the virulent virus. Polynucleotide vaccine technology provides a unique opportunity to produce vaccines against flavivirus diseases of low incidence cheaply and rapidly, and to produce multivalent vaccines such as would be required for immunisation against dengue virus disease.
通过肌肉注射表达微生物病原体免疫原性蛋白的质粒进行体内转染,作为一种针对人和动物多种病原体的疫苗接种策略具有相当大的潜力。在此我们报告,给断奶小鼠单次肌肉注射50微克在巨细胞病毒立即早期蛋白启动子控制下表达圣路易斯脑炎病毒(SLE)prM/E蛋白的质粒pSLE1,可产生SLE特异性抗体,并能抵御强毒病毒的致死性攻击。多核苷酸疫苗技术为廉价、快速生产针对低发黄病毒疾病的疫苗以及生产如登革病毒疾病免疫所需的多价疫苗提供了独特机会。