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作 者:赵佳琪[1] 王婉莹[1] 范业宁 马春平[1] 张东红[1] 吕扬[1] 赵臣[1]
出 处:《重庆医学》2017年第19期2612-2614,共3页Chongqing medicine
基 金:吉林省科技厅自然科学基金资助项目(20160101179JC);吉林省卫生和计划生育委员会项目(2015Z071);吉林省教育厅"十三五"科技项目(JJKH20170416KJ);吉林省大学生创新创业课题(2015024);国家级大学生创新创业训练计划项目(201613706019)
摘 要:目的构建pIRES2-MLAA34-HSP70重组质粒,并检测其免疫效果。方法采用逆转录PCR(RT-PCR)的方法提取急性单核细胞白血病相关抗原基因MLAA-34和热休克蛋白(HSP)70基因,设计特异性重叠引物,以重叠延伸PCR(SOEPCR)技术扩增MLAA34-HSP70融合基因,构建核酸疫苗pIRES2-MLAA34-HSP70。将核酸疫苗免疫BALB/c小鼠,检测小鼠脾淋巴细胞对U937细胞的杀伤作用及小鼠脾细胞悬液中白细胞介素(IL)-2、IL-4和γ干扰素(IFN-γ)水平。结果扩增出MLAA34-HSP70融合基因2 956bp,成功构建了核酸疫苗pIRES2-MLAA34-HSP70,经鉴定与预期结果一致;脾淋巴细胞杀伤活性结果显示,核酸疫苗pIRES2-MLAA34-HSP70对U937细胞的杀伤效率明显高于其他实验组及对照组(P<0.01);核酸疫苗pIRES2-MLAA34-HSP70组细胞因子IL-2、IL-4和IFN-γ水平亦明显高于其他实验组及对照组(P<0.01)。结论成功构建了pIRES2-MLAA34-HSP70核酸疫苗,该核酸疫苗能诱发强烈的体液免疫,增强机体对肿瘤细胞的免疫应答,对MLAA34阳性细胞具有特异性杀伤作用。Objective To construct the DNA vaccine plRES2-MLAA34-HSP70,and to detect its immune effect. Methods The acute monocytic leukemia associated antigen gene MLAA-34 and heat-shock protein (HSP)70 gene were extracted by using RT-PCR. The specific overlapping primer was designed, and the fusion gene MLAA34-HSP70 was amplified by using SOE-PCR technique. Then the DNA vaccine plRES2-MLAA34-HSP70 was constructed, and BALB/c mice were immunized with this DNA vaccine. The splenic lymphocyte killing activity was detected by using MTT,levels of IL-2, IL-4 and IFN-], were also detected by u- sing ELISA. Results The MLAA34-HSP70 gene (2 956 bp) and the DNA vaccine pIRES2-MLAA34-HSP70 was amplified and constructed successfully. The killing efficiency of DNA vaccine pIRES2-MLAA34-HSPT0 in U937 cells was significantly higher than that in other experimental groups and control group (P〈0. 01) ,and levels of IL-4, IL-2 and IFN-7 in DNA vaccine pIRES2- MLAA34-HSP70 group were significantly higher than those in the other experimental groups and control group (P〈0.01). Con- clusion The DNA vaccine pIRES2-MLAA34-HSP70 is constructed successfully. It is shown that the DNA vaccine induces strong humoral immunity,which could enhance immune responses to tumor cells and specificlly kill MLAA34 positive cells.
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