Liu Shuojie, Cheng Jizhong, Tang Chengwu
Department of Biochemistry and Molecular Biology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
J Huazhong Univ Sci Technolog Med Sci. 2007 Dec;27(6):625-9. doi: 10.1007/s11596-007-0601-4.
To find a new preventive strategy for the infection of Schistosoma japonica, plasmid pIRES-Sj97-Sj14-Sj26 that contains fatty binding protein (Sj14), GST (Sj26) and paramyocin (Sj97) that are expressed on the membrane, was constructed. RT-PCR was used to detect the expression of Sj14 mRNA, Sj26 mRNA and Sj97 mRNA in the Hela cells, the indirect immunofluorescent test was employed for the detection of the expression of trans-membrane Sj26 after the plasmid was transfected into Hela cells. Fifty BALB/c mice were randomly divided into 5 groups and pIRES-Sj97-Sj14-Sj26 plasmid DNA, pIRES-Sj14-Sj26 plasmid DNA, pIRES-Sj26 plasmid DNA, pIRES blank vector and normal saline were respectively injected into the quadriceps muscles of thigh. Eight weeks after the immunization the mice were killed and significantly higher level of IgG was detected in the pIRES-Sj97-Sj14-Sj26 group as compared with the pIRES blank vector, normal saline and pIRES-Sj26 groups (P<0.01) and the pIRES-Sj14-Sj26(P<0.05). Single splenocyte suspension was prepared to detected the level of IFN-gamma by ELISA and the lymphocyte stimulating index (SI) by MTT. SI was significantly higher of in the pIRES-Sj97-Sj14-Sj26 group than in other groups (P<0.01), while the IFN-gamma level was significantly higher the pIRES-Sj97-Sj14-Sj26 group than in pIRES blank vector and normal saline groups (P<0.01), but no significant differences were found when compared with pIRES-Sj14-Sj26 and pIRES-Sj26 groups. Flow cytometery showed that the percent-ages of CD4+ and CD8+ T cells were much higher in the pIRES-Sj97-Sj14-Sj26 group (P< 0.01, P<0.05). It was concluded that pIRES-Sj97-Sj14-Sj26 vaccine may induce stronger immune response in BALB/c mice.
为寻找日本血吸虫感染的新预防策略,构建了含有膜表达的脂肪酸结合蛋白(Sj14)、谷胱甘肽S-转移酶(GST,Sj26)和副肌球蛋白(Sj97)的质粒pIRES-Sj97-Sj14-Sj26。采用RT-PCR检测Hela细胞中Sj14 mRNA、Sj26 mRNA和Sj97 mRNA的表达,质粒转染Hela细胞后采用间接免疫荧光试验检测跨膜Sj26的表达。将50只BALB/c小鼠随机分为5组,分别将pIRES-Sj97-Sj14-Sj26质粒DNA、pIRES-Sj14-Sj26质粒DNA、pIRES-Sj26质粒DNA、pIRES空载体和生理盐水注射到大腿股四头肌中。免疫8周后处死小鼠,与pIRES空载体、生理盐水和pIRES-Sj26组相比,pIRES-Sj97-Sj14-Sj26组检测到的IgG水平显著升高(P<0.01),与pIRES-Sj14-Sj26组相比差异有统计学意义(P<0.05)。制备单个脾细胞悬液,采用ELISA检测IFN-γ水平,采用MTT检测淋巴细胞刺激指数(SI)。pIRES-Sj97-Sj14-Sj26组的SI显著高于其他组(P<0.01),而pIRES-Sj97-Sj14-Sj26组的IFN-γ水平显著高于pIRES空载体和生理盐水组(P<0.01),但与pIRES-Sj14-Sj26组和pIRES-Sj26组相比无显著差异。流式细胞术显示,pIRES-Sj97-Sj14-Sj26组CD4+和CD8+T细胞百分比显著更高(P<0.01,P<0.05)。结论:pIRES-Sj97-Sj14-Sj26疫苗可诱导BALB/c小鼠产生更强的免疫反应。