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DNA疫苗与修饰重组蛋白的异源初免-加强免疫增强小鼠对……的免疫反应。 (原文中against后缺少具体内容)

Heterologous Prime-Boost Immunization with DNA Vaccine and Modified Recombinant Proteins Enhances Immune Response against in Mice.

作者信息

Huang Ting, Zhao Kelei, Song Xuhao, Song Tao, Wang Xinrong, Zhang Xiuyue, Yue Bisong, Chu Yiwen

机构信息

Antibiotics Research and Re-Evaluation Key Laboratory of Sichuan Province, School of Pharmacy, Chengdu University, Chengdu 610052, China.

Key Laboratory of Southwest China Wildlife Resources (Ministry of Education), China West Normal University, Nanchong 637002, China.

出版信息

Vaccines (Basel). 2022 May 25;10(6):839. doi: 10.3390/vaccines10060839.

Abstract

() is a crucial opportunistic pathogen normally causing mastitis, abscesses and pneumonia in economically important ruminants. Although only one commercial vaccine of is currently obtainable, its immunoprotective effect is limited. Pyolysin (PLO) is the most predominant virulence factor highly expressed in and is an excellent target for the development of novel vaccines against . In this study, we designed a heterologous prime-boost vaccination scheme combining a DNA vaccine pVAX1-PLO and a subunit vaccine His-PLO to maximize host responses in mice. Humoral and cellular immune responses and protective effects were evaluated in mice to compare the immunogenicity induced by different immunization schemes. Compared to the PBS-control group, in vivo immunization results showed that better immune responses of mice immunized with the pVAX1-PLO plasmids and His-PLO proteins were induced. The residual bacterial burdens from the liver and peritoneal fluid were remarkably decreased in the immunized mice compared with the PBS group. Notably, the heterologous prime-boost vaccination groups significantly enhanced host humoral and cellular immune responses and protected mice from different virulent strains infection. Conclusively, this study provides a favorable strategy for the further development of next-generation vaccines against infections.

摘要

(某病原体名称)是一种关键的机会性病原菌,通常会在具有重要经济价值的反刍动物中引发乳腺炎、脓肿和肺炎。尽管目前仅有该病原体的一种商业疫苗可供使用,但其免疫保护效果有限。溶血素(PLO)是在该病原体中高度表达的最主要毒力因子,是开发针对该病原体新型疫苗的理想靶点。在本研究中,我们设计了一种异源初免-加强免疫接种方案,将DNA疫苗pVAX1-PLO和亚单位疫苗His-PLO相结合,以最大化小鼠体内的宿主反应。在小鼠中评估了体液和细胞免疫反应以及保护作用,以比较不同免疫方案诱导的免疫原性。与PBS对照组相比,体内免疫结果表明,用pVAX1-PLO质粒和His-PLO蛋白免疫的小鼠诱导出了更好的免疫反应。与PBS组相比,免疫小鼠肝脏和腹腔液中的残留细菌载量显著降低。值得注意的是,异源初免-加强免疫接种组显著增强了宿主的体液和细胞免疫反应,并保护小鼠免受不同毒力的该病原体菌株感染。总之,本研究为进一步开发针对该病原体感染的下一代疫苗提供了一种有利策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cae0/9230664/7ab8963fd391/vaccines-10-00839-g001.jpg

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