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作 者:邓涛[1] 陈乃玲[1] 陈天宝[1] 武珊珊 张哓红 刘倩[1] 贾克明[1]
机构地区:[1]中国人民解放军肝病研究所
出 处:《中国公共卫生学报》1998年第1期13-15,共3页
基 金:国家自然科学基金
摘 要:将经过基因修饰的乙肝病毒核心区基因定向克隆于质粒pcDNA3巨细胞病毒启动子下游,构建成真核表达载体,称为pcDNA3-HBV。将pcDNA3-HBV通过多点肌肉注射,给BALB/c小鼠免疫接种100μg/只,2周后追加免疫1次,追加免疫1周后8只免疫鼠中7只出现抗-HBcIgG血清转化,而接种空载质粒pcDNA3的对照组及未经任何免疫接种的BALB/c小鼠无一只抗-HBcIgG阳性。The modificated HBc gene with its stem and loopstructure trancated was inserted into the eukaryotic expression vector under the CMV promotor between the Hind Ⅲ and Bam HI site (pcDNA3HBV).The Balb/c mice were immunized by multiple sites intramuscular injection with pcDNA3HBV and pcDNA3 respectively.Each mouse was injected with 100μg DNA(1μg/μl in PBS).Another 100μg DNA were reinjected after 2 weeks.The antiHBc IgG were detected by ELISA in 7 out of 8 immunized mice (pcDNA3HBV group)after 7 days,but no antiHBc IgG Ab could be measured in pcDNA3 immunized group(n=4) and nonimmunized group(n=4)
分 类 号:R512.620.5[医药卫生—内科学]
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