HBV截短core基因融合preS1基因在BCG中的表达及其免疫应答  被引量:2

Immune response in BALB/c mice immunized with BCG expressing HBV truncated C gene and preS1 gene

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作  者:尹文[1] 吕欣[2] 雷迎峰[2] 杨敬[2] 孙梦宁[2] 马玉[2] 兰海云[1] 汪爱勤[1] 

机构地区:[1]第四军医大学基础部中心实验室,陕西西安710032 [2]第四军医大学基础部微生物学与病原生物学教研室,陕西西安710032

出  处:《细胞与分子免疫学杂志》2010年第1期28-30,共3页Chinese Journal of Cellular and Molecular Immunology

基  金:国家自然科学基金资助项目(30671878;30670100)

摘  要:目的:探讨HBV相关抗原在卡介苗(BCG)中的有效表达及其刺激产生的体液和细胞免疫应答效果。方法:将带有HBV截短C基因和preS1基因片段的穿梭载体转化BCG菌株,筛选重组菌,SDS-PAGE和Western blot实验分析其抗原表达特性;分别以生理盐水、BCG、BCG-pDE22、BCG-pDE22-CS1皮下注射BALB/c小鼠,进行连续抗体测定和细胞毒性T细胞杀伤实验。结果:与对照组相比,重组BCG可表达Mr为24000的新生蛋白,与CS1融合蛋白大小相符,Westernblot实验分析显示出良好的抗原结合特性;带有HBVCS1抗原基因的重组BCG免疫组抗体滴度显著升高,特异性杀伤能力更强。结论:BCG可以作为HBV相关抗原的活载体,为研制HBV新型疫苗提供了实验依据。AIM:To study expressing of HBV truncated core and preS1 protein in BCG and to explore the effect of humoral and cellular immune response stimulated by the recombinant BCG.METHODS:A shuttle vector was constructed and was transformed into BCG which including truncated Core gene and preS1 gene of HBV.The recombinant BCGs were analyzed with SDS-PAGE and Western blot.The three groups of BALB/c mice were immunized with saline,BCG,BCG-pDE22 and BCG-pDE22-CS1 respectively.Then the antibody titer and CTL effects were evaluated.RESULTS:Compared with the control group,the recombinant BCG could express a new protein band of 24 kD which was consistent with the size of CS1 fused protein which displayed a good antigen-binding property by Western blot analysis.The antibody titer significantly increased and CTL effect apparently enhanced in the recombinant BCG immunized group.CONCLUSION:BCG could be as live vector which carrying HBV related genes,which developing a novel vaccine against HBV.

关 键 词:乙型肝炎病毒 细胞毒性T细胞 BCG 抗体 

分 类 号:R392.11[医药卫生—免疫学]

 

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