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用聚甲基丙烯酸甲酯配制的DNA疫苗在免疫后以及用硕大利什曼原虫攻击后的免疫反应。

Immune responses in DNA vaccine formulated with PMMA following immunization and after challenge with Leishmania major.

作者信息

Zarrati Somayeh, Mahdavi Mehdi, Tabatabaie Fatemeh

机构信息

Microbiology Department, Science & Research Branch, Islamic Azad University, Tehran, Iran.

Virology Department, Pasteur Institute of Iran, Tehran, Iran.

出版信息

J Parasit Dis. 2016 Jun;40(2):427-35. doi: 10.1007/s12639-014-0521-8. Epub 2014 Aug 31.

Abstract

Leishmaniasis is a major infectious disease caused by protozoan parasites of the genus Leishmania. Despite of many efforts toward vaccine against Leishmania no effective vaccine has been approved yet. DNA vaccines can generate more powerful and broad immune responses than conventional vaccines. In order to increase immunity, the DNA vaccine has been supplemented with adjuvant. In this study a new nano-vaccine containing TSA recombinant plasmid and poly(methylmethacrylate) nanoparticles (act as adjuvant) was designed and its immunogenicity tested on BALB/c mouse. After three intramuscular injection of nano-vaccine (100 μg), the recombinant TSA protein (20 μg) was injected subcutaneously. Finally as a challenge animals were infected by Leishmania major. After the last injection of nano-vaccine, after protein booster injection, and also after challenge, cellular immune and antibody responses were evaluated by ELISA method. The findings of this study showed the new nano-vaccine was capable of induction both cytokines secretion and specific antibody responses, but predominant Th1 immune response characterized by IFN-γ production compared to control groups. Moreover, results revealed that nano-vaccine was effective in reducing parasite burden in the spleen of Leishmania major-infected BALB/c mice. Base on results, current candidate vaccine has potency for further studies.

摘要

利什曼病是由利什曼原虫属的原生动物寄生虫引起的一种主要传染病。尽管在研发针对利什曼原虫的疫苗方面付出了诸多努力,但尚未有有效的疫苗获批。DNA疫苗能够产生比传统疫苗更强大、更广泛的免疫反应。为了增强免疫力,DNA疫苗已添加佐剂。在本研究中,设计了一种包含TSA重组质粒和聚甲基丙烯酸甲酯纳米颗粒(作为佐剂)的新型纳米疫苗,并在BALB/c小鼠身上测试了其免疫原性。在三次肌肉注射纳米疫苗(100μg)后,皮下注射重组TSA蛋白(20μg)。最后,作为攻毒,动物被大型利什曼原虫感染。在最后一次注射纳米疫苗后、蛋白加强注射后以及攻毒后,通过ELISA方法评估细胞免疫和抗体反应。本研究结果表明,新型纳米疫苗能够诱导细胞因子分泌和特异性抗体反应,但与对照组相比,以产生IFN-γ为特征的Th1免疫反应占主导。此外,结果显示纳米疫苗在降低大型利什曼原虫感染的BALB/c小鼠脾脏中的寄生虫负荷方面是有效的。基于这些结果,当前的候选疫苗有进一步研究的潜力。

相似文献

本文引用的文献

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A review of adjuvants for Leishmania vaccine candidates.利什曼原虫疫苗候选佐剂综述。
J Biomed Res. 2010 Jan;24(1):16-25. doi: 10.1016/S1674-8301(10)60004-8.
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PMMA particle-mediated DNA vaccine for cervical cancer.
J Biomed Mater Res A. 2009 Mar 15;88(4):849-57. doi: 10.1002/jbm.a.31919.

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