| 日本血吸虫中国大陆株23 kDa膜蛋白DNA疫苗诱导小鼠保护性免疫的研究 |
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| 引用本文： | 任建功,朱荫昌,D.A.Harn,余传信,殷旭仁,司进,何伟,徐明,华万全,许永良. 日本血吸虫中国大陆株23 kDa膜蛋白DNA疫苗诱导小鼠保护性免疫的研究[J]. 中国寄生虫学与寄生虫病杂志, 2001, 19(6): 336-339 |
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| 作者姓名： | 任建功 朱荫昌 D.A.Harn 余传信 殷旭仁 司进 何伟 徐明 华万全 许永良 |
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| 作者单位： | 1. 江苏省血吸虫病防治研究所,无锡,214064
2. 美国哈佛大学公共卫生学院 |
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| 基金项目： | 获世界卫生组织/世界银行/热带病研究和培训特别规划署(TDR)资助(No.981051)以及江苏省卫生厅科教处(No.-H9918)和科技厅应用基础基金的部分资助(No.BJ98034) |
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| 摘 要： | 目的 研究日本血吸虫中国大陆株 2 3kDa膜蛋白 (SjC2 3)DNA疫苗诱导C5 7BL/6小鼠免疫保护作用。方法 将全长的SjC2 3基因克隆到真核表达载体pcDNA3.1,构建DNA疫苗 pcDNA3.1 SjC2 3。制备SjC2 3及IL 12的两个亚单位 p35、p4 0的DNA疫苗和对照 pcDNA3.1。 4 8只C5 7BL/6小鼠随机分为A、B、C 3组。A组小鼠肌注 10 0 μgpcDNA3.1;B组注射 10 0 μg pcDNA3.1 SjC2 3;C组肌注 pcDNA3.1 SjC2 3、pcDNA3.1 p35及pcDNA3.1 p4 0各 10 0 μg的混合物。每隔 2周各免疫 1次 ,共 3次。第 8周每鼠感染 4 5± 2条 /只尾蚴 ,4 5d后剖杀 ,计数成虫及肝内虫卵。采用免疫组化法检测SjC2 3及 p35、p4 0在小鼠局部组织内的表达 ;用脾细胞培养法检测经rSjC2 3 HD刺激后 ,攻击前、后小鼠脾细胞IL 2、IL 4、IL 10和IFN γ的水平。用Westernblotting检测血清中抗SjC2 3抗体。结果 SjC2 3以及p35、p4 0在免疫小鼠股四头肌细胞膜和细胞浆均获得表达。IL 2和IFN γ的水平攻击前、后在B组和C组均明显升高。Westernblotting检测抗SjC2 3抗体结果表明 ,免疫后两周 ,B组 8/10份血清为阳性 ,C组 9/10份血清阳性。B组和C组分别获得 2 6 .9%和 35 .4 %的减虫率 ,C组显著高于B组 (P <0 .0 5 ) ;减卵率分别为 2 2 .2 %和 2 8.4 %。结论 SjC
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| 关 键 词： | 日本血吸虫 23kDa膜蛋白 DNA疫苗 保护性免疫 |
| 文章编号： | 1000-7423(2001)-06-0336-04 |
Protective Immunity Induced by 23 kDa Membrane Protein DNA Vaccine of Schistosoma japonicum Chinese Strain in Mice |
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| REN Jian gong,ZHU Yin chang,D.A.Harn,YU Chuan xin,YIN Xu ren,SI Jin,HE Wei,XU Ming,HUA Wan quan,XU Yong liang. Protective Immunity Induced by 23 kDa Membrane Protein DNA Vaccine of Schistosoma japonicum Chinese Strain in Mice[J]. Chinese Journal of Parasitology and Parasitic Diseases, 2001, 19(6): 336-339 |
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| Authors: | REN Jian gong ZHU Yin chang D.A.Harn YU Chuan xin YIN Xu ren SI Jin HE Wei XU Ming HUA Wan quan XU Yong liang |
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| Affiliation: | Jiangsu Institute of Parasitic Diseases, Wuxi 214064. |
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| Abstract: | OBJECTIVE: To develop 23 kDa membrane protein DNA vaccine of Schistosoma japonicum Chinese strain and test its protective efficacy in infected C57BL/6 mice. METHODS: The full length cDNA encoding SjC23 amplified from pUC19-SjC23 subcloned into pcDNA3.1. 48 female mice were divided into three groups: A, B and C. Group A (control group) was each immunized i.m. with 100 micrograms of pcDNA3.1; group B (SjC23 group) was each immunized i.m. with 100 micrograms of pcDNA3.1-SjC23; group C (SjC23 + IL-12) was each immunized i.m. with a mixture of 100 micrograms of pcDNA3.1-SjC23, 100 micrograms of pcDNA3.1-p35 and 100 micrograms of pcDNA-p40, followed by two boosts of the same DNA once every two weeks. All the mice were challenged with 45 cercariae at week 8, killed and perfused for worms at week 14. The expression of SjC23 and p35, p40 in muscle tissue was determined by immuno-histochemical method. By the culture of spleen cells, the production of IL-2, IL-4, IL-10 and IFN-gamma after the stimulation of rSjC23-HD was determined two weeks before and after challenge. Anti-SjC23 antibodies were tested by Western blotting. RESULTS: SjC23 and p35, p40 were all expressed on the membrane and in the plasma of muscle cells of the infected mice. Significant increase of IL-2 and IFN-gamma in SjC23 and SjC23 + IL-12 groups was observed before and after challenge. Western blotting showed that after the third immunization (before challenge) 8 out of 10 sera from SjC23 group and 9 out of 10 sera from SjC23 + IL-12 group were positive. The worm reduction rate in SjC23 group and SjC23 + IL-12 group was 26.9% and 35.4%, respectively; the number of eggs in liver tissue was reduced by 22.2% and 28.4%, respectively. CONCLUSION: pcDNA3.1-SjC23 DNA vaccine could induce partial protection against Schistosoma japonicum in C57BL/6 mice. |
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| Keywords: | Schistosoma japonicum 23 kDa membrane protein DNA vaccine protective immunity |
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