首页 | 本学科首页   官方微博 | 高级检索  
     

日本血吸虫TPI DNA疫苗基因密码子优化增强免疫保护作用的研究
引用本文:鲁飞,朱荫昌,戴洋,王晓婷,唐建霞,张纯. 日本血吸虫TPI DNA疫苗基因密码子优化增强免疫保护作用的研究[J]. 中国寄生虫学与寄生虫病杂志, 2009, 27(3): 189-194
作者姓名:鲁飞  朱荫昌  戴洋  王晓婷  唐建霞  张纯
作者单位:江苏省血吸虫病寄生虫病防治研究所、卫生部寄生虫病预防与控制技术重点实验室、江苏省寄生虫分子生物学重点实验室、江苏省寄生虫病重点学科,无锡 214064
摘    要:目的  研究日本血吸虫中国大陆株磷酸丙糖异构酶基因(TPI基因)密码子优化后的DNA疫苗增强免疫保护作用的效果。 方法  60只BALB/c雌性小鼠随机均分为A(pcDNA3.1空质粒对照组)、B(pcDNA3.1-TPI组)、C (pcDNA3.1-TPI-mHSP70组)、D(pcDNA3.1-TPI.opt组)、E(pcDNA3.1-TPI.opt-mHSP70组)等5组。每鼠肌肉注射相应的纯化质粒DNA 100 μg,每隔3周免疫1次,共3次。末次免疫后4周,每鼠经腹部皮肤攻击感染日本血吸虫尾蚴(40±1)条,42 d后剖杀,计数成虫及肝脏虫卵数。首次免疫前2 d及感染前2 d经尾静脉采血,检测IgG及IgG1、IgG2a的水平。攻击感染前2 d取脾脏,制备单个脾细胞,用流式细胞仪检测白细胞介素2(IL-2)、IL-4、IL-5、γ干扰素(IFN-γ)及肿瘤坏死因子(TNF)的水平。 结果  B、C、D、E组小鼠血清均检测到特异性IgG及IgG2a与IgG1抗体,IgG2a/IgG1的比值分别为1.73、2.06、2.44、3.09。D、E组的IL-2、IFN-γ、TNF含量较B、C组均有不同程度地升高。D、E组减虫率分别为36.03%、39.03%,减卵率分别为41.71%、46.85%,均显著高于B、C组(P<0.01)。 结论 TPI基因密码子优化后的DNA疫苗相对于未优化TPI DNA疫苗能诱导小鼠产生较高的免疫保护作用,且诱导宿主产生较强的,及以Th1为主的免疫应答。

关 键 词:日本血吸虫;密码子优化;免疫保护

Enhancing Protective Immunity Effects of TPI DNA Vaccine against Schistosoma japonicum through Codon Optimization
LU Fei,ZHU Yin-chang,DAI Yang,WANG Xiao-ting,TANG Jian-xia,ZHANG Chun. Enhancing Protective Immunity Effects of TPI DNA Vaccine against Schistosoma japonicum through Codon Optimization[J]. Chinese Journal of Parasitology and Parasitic Diseases, 2009, 27(3): 189-194
Authors:LU Fei  ZHU Yin-chang  DAI Yang  WANG Xiao-ting  TANG Jian-xia  ZHANG Chun
Affiliation:Jiangsu Institute of Parasitic Diseases, Key Laboratory on Technology for Parasitic Disease Prevention and Control,Ministry of Health,Jiangsu Provincial Key Laboratory on Molecular Biology of Parasites,Jiangsu Provincial Key Subject on Parasitic Diseases,Wuxi 214064,China
Abstract:Objective To study the protective effect of codon optimized TPI DNA vaccine against Schistosoma japonicum infection. Methods Sixty female BALB/c mice were randomly divided into 5 groups. The mice were injected through musculus quadriceps fexoris with 100 μg pcDNA 3.1 control(Group A),pcDNA3.1-TPI(Group B),pcDNA 3.1-TPI-mHSP70(Group C),pcDNA3.1-TPI.opt(Group D),and pcDNA3.1-TPI.opt-mHSP70(Group E)respectively. All mice were immunized for three times with an interval of two weeks. The mice were challenged with(40±1) cercariae of S. japonicum per mouse by abdominal skin penetration 4 weeks after the last immunization,and sacrificed at 42 days post-challenge,the number of worms or hepatic eggs was counted. Blood was taken for the detection of IgG,IgG1,and IgG2a 2 days before immunization and before challenge,respectively. Spleen cells of 2 mice from each group were cultured and stimulated with ConA and rSjCTPI peptide,and the supernatant was collected for detection of IL-2,IL-4,IL-5,IFN-γ,and TNF by flow cytometry. Results ELISA showed that the mice in groups B,C,D,and E produced specific IgG and IgG1,IgG2a antibody isotypes,and the ratio of IgG2a/IgG1 was 1.73,2.06,2.44,and 3.09,respectively. The levels of IL-2,IFN-γ and TNF in groups D and E were higher than that of groups B and C. The worm reduction rate and hepatic egg reduction rate in groups D(36.03%,41.7%) and E(39.03%,46.85%)were higher than those of groups B(26.28%,28.35%) and C(28.38%,31.39%)(P<0.01). Conclusions The codon optimized TPI DNA vaccine induces higher level of protective effect and Th1-biased cellular immune response than those of non-optimized TPI DNA vaccine.
Keywords:Schistosoma japonicum;Codon optimization;Protective immunity
点击此处可从《中国寄生虫学与寄生虫病杂志》浏览原始摘要信息
点击此处可从《中国寄生虫学与寄生虫病杂志》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号