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[免疫刺激序列增强日本血吸虫 SjC23 DNA 疫苗的抗感染保护作用]

[Enhancement of the protective effect of SjC23 DNA vaccine against Schistosoma japonicum infection by immunostimulatory sequence].

作者信息

Zhao Song, Zhu Yin-chang, Harn Donald A, Si Jin, Ren Jian-gong, Yin Xu-ren, He Wei, Liang You-sheng, Xu Ming, Xu Yong-liang

机构信息

Jiangsu Institute of Parasitic Diseases, Wuxi 214064, China.

出版信息

Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi. 2005 Feb 28;23(1):1-5.

Abstract

OBJECTIVE

To investigate the effect of immunostimulatory sequence on SjC23 DNA vaccine against Schistosoma japonicum infection.

METHODS

SjC23 gene fragment was inserted into pcDNA3. 1-CpG to construct pcDNA3.1-SjC23/CpG. BALB/c mice in 4 groups were immunized intramuscularly 3 times at 2 week intervals, with 100 microg plasmid DNA per injection. Four weeks after the 3rd immunization, all mice were challenged with 45 +/- 1 cercariae of S. japonicum by abdominal skin penetration. After 45 days post-challenge, mice were perfused and the number of recovered worms and of eggs in liver was counted. Blood samples were collected from the tail vein of all mice 2 days before the 1st immunization and before challenge respectively. IgG, IgG1 and IgG2a in sera were detected. Three weeks after the 3rd inoculation, the spleen cells of 2 mice from each group were cultured and stimulated with ConA and recombinant peptide. The supernatant was collected to detect IL-2, IL-4 and IFN-gamma. Simultaneously, the cytotoxic activity was detected with 51Cr release assay in vitro.

RESULTS

The worm reduction rate in SjC23 group and SjC23/CpG group was 28.1% and 35.1%, the hepatic egg reduction rate was 21.6% and 26.5%, respectively, compared with the control group. The level of protection in SjC23/CpG group was higher than that in SjC23 group (P<0.05). ELISA results indicated that mice immunized with pcDNA3.1-SjC23 and SjC23/CpG produced specific IgG to rSjC23, while mice immunized with pcDNA3.1 and pcDNA3.1-CpG did not. Mice in SjC23 group and SjC23/CpG group also produced IgG1 and IgG2a antibody isotypes, with the ratio of IgG2a/IgG1 10.1 and 12.2, respectively. In comparison with the control, the level of IL-2 and IFN-gamma in mice immunized with pcDNA3.1-SjC23 and pcDNA3.1-SjC23/CpG was augmented. The cytotoxic activity of spleen cells from mice in SjC23/CpG group was augmented from 9.7% to 40.0% compared with that in SjC23 group.

CONCLUSION

The study indicates that immunostimulatory sequence appears to increase the level of protection induced by immunization with pcDNA3.1-SjC23 vaccine.

摘要

目的

探讨免疫刺激序列对日本血吸虫感染的SjC23 DNA疫苗的影响。

方法

将SjC23基因片段插入pcDNA3.1-CpG构建pcDNA3.1-SjC23/CpG。4组BALB/c小鼠每隔2周肌肉注射免疫3次,每次注射100μg质粒DNA。第3次免疫后4周,所有小鼠经腹部皮肤穿刺用45±1条日本血吸虫尾蚴攻击。攻击后45天,对小鼠进行灌注,计数回收的虫体数量和肝脏中的虫卵数量。分别在第1次免疫前2天和攻击前从所有小鼠尾静脉采集血样。检测血清中的IgG、IgG1和IgG2a。第3次接种后3周,每组取2只小鼠的脾细胞进行培养,用ConA和重组肽刺激。收集上清液检测IL-2、IL-4和IFN-γ。同时,体外采用51Cr释放试验检测细胞毒性活性。

结果

与对照组相比,SjC23组和SjC23/CpG组的减虫率分别为28.1%和35.1%,肝脏减卵率分别为21.6%和26.5%。SjC23/CpG组的保护水平高于SjC23组(P<0.05)。ELISA结果表明,用pcDNA3.1-SjC23和SjC23/CpG免疫的小鼠产生了针对rSjC23的特异性IgG,而用pcDNA3.1和pcDNA3.1-CpG免疫的小鼠则未产生。SjC23组和SjC23/CpG组的小鼠也产生了IgG1和IgG2a抗体亚型,IgG2a/IgG1的比值分别为10.1和12.2。与对照组相比,用pcDNA3.1-SjC23和pcDNA3.1-SjC23/CpG免疫的小鼠中IL-2和IFN-γ水平升高。与SjC23组相比,SjC23/CpG组小鼠脾细胞的细胞毒性活性从9.7%提高到40.0%。

结论

该研究表明免疫刺激序列似乎可提高pcDNA3.1-SjC23疫苗免疫诱导的保护水平。

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