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pVAX/ERK7诱导的BALB/c小鼠抗感染免疫反应。

Immune Responses Induced by pVAX/ERK7 against Infection in BALB/c Mice.

作者信息

Guo Hai-Ting, Li Zhong-Yuan, Wang Jin-Lei, Geng Zhao-Yu, Zhu Xing-Quan

机构信息

Guangxi Key Laboratory for Brain and Cognitive Neurosciences, Guilin Medical College, Guilin, China.

College of Biological Science and Technology, Heilongjiang Bayi Agricultural University, Daqing, China.

出版信息

Iran J Parasitol. 2019 Oct-Dec;14(4):552-562.

Abstract

BACKGROUND

can infect all the warm-blooded vertebrates and cause serious toxoplasmosis. Extracellular signal-regulated kinase 7 in (ERK7) mediated the proliferation of this parasite may be a potential vaccine candidate. Thus, immune responses induced by ERK7 were investigated in this study using a DNA vaccine strategy.

METHODS

pVAX/ERK7 plasmid was constructed and used to immunize BALB/c mice for three times with two-week intervals. The challenge and the investigation of humoral and cellular immune responses were performed at two weeks post the last immunization, and the survival times of the infected mice were daily recorded until all of them were dead.

RESULTS

The innate immune response with higher concentrations of IFN-γ, TNF-α, IL2 and IL12p70 in sera ( < 0.05), and the adaptive immune responses were evoked by the DNA immunizations, including specific antibody, lymphocyte proliferation, and the CD3e+CD4+ and CD3e+CD8a+ T cell-mediated response effects. Interestingly, no significant difference was detected in their survival times among all the experimental groups of mice that were challenged with GT1 tachyzoites or PRU cysts (>0.05).

CONCLUSION

The successive immunizations with pVAX/ERK7 can provoke the innate and adaptive immune responses of BALB/c mice, whereas the DNA vaccine-induced immunological efficacy is not sufficient for complete protection the host against infection.

摘要

背景

可感染所有温血脊椎动物并引起严重的弓形虫病。细胞外信号调节激酶7(ERK7)介导该寄生虫的增殖,可能是一种潜在的疫苗候选物。因此,本研究采用DNA疫苗策略研究了ERK7诱导的免疫反应。

方法

构建pVAX/ERK7质粒,用于免疫BALB/c小鼠,每隔两周免疫一次,共免疫三次。在最后一次免疫后两周进行攻毒,并检测体液免疫和细胞免疫反应,每天记录感染小鼠的存活时间,直至全部死亡。

结果

DNA免疫诱导了固有免疫反应,血清中IFN-γ、TNF-α、IL2和IL12p70浓度升高(P<0.05),以及适应性免疫反应,包括特异性抗体、淋巴细胞增殖以及CD3e+CD4+和CD3e+CD8a+T细胞介导的反应效应。有趣的是,在用GT1速殖子或PRU包囊攻毒的所有实验组小鼠中,其存活时间未检测到显著差异(P>0.05)。

结论

连续用pVAX/ERK7免疫可激发BALB/c小鼠的固有免疫和适应性免疫反应,而DNA疫苗诱导的免疫效果不足以完全保护宿主免受弓形虫感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64e0/7028233/d7e0652986da/IJPA-14-552-g001.jpg

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