Suppr超能文献

FNBPA(pValac:)在小鼠口服免疫后诱导细胞免疫和体液免疫反应。

FNBPA (pValac:) Induces Cellular and Humoral Immune Responses After Oral Immunization of Mice.

作者信息

de Castro Camila Prósperi, Souza Bianca Mendes, Mancha-Agresti Pamela, Pereira Vanessa Bastos, Zurita-Turk Meritxell, Preisser Tatiane Melo, da Cunha Vanessa Pecini, Dos Santos Janete Soares Coelho, Leclercq Sophie Yvette, Azevedo Vasco, Miyoshi Anderson

机构信息

Laboratory of Genetic Technology, Department of Genetics, Ecology and Evolution, Institute of Biological Sciences, Federal University of Minas Gerais (UFMG), Belo Horizonte, Brazil.

Laboratory of Cellular and Molecular Genetics, Department of Genetics, Ecology and Evolution, Institute of Biological Sciences, Federal University of Minas Gerais (UFMG), Belo Horizonte, Brazil.

出版信息

Front Microbiol. 2021 May 20;12:676172. doi: 10.3389/fmicb.2021.676172. eCollection 2021.

Abstract

The development of a new vaccine strategy against tuberculosis is urgently needed and has been greatly encouraged by the scientific community worldwide. In this work, we constructed a lactococcal DNA vaccine based on the fusion of two antigens, ESAT-6 and Ag85A, and examined its immunogenicity. The coding sequences of the and genes were fused and cloned into the eukaryotic expression pValac vector, and the functionality of the vector was confirmed . Then, FnBPA (pValac:) was obtained and used for oral immunization of mice. This strain induced significant increases in IFN-γ, TNF-α, and IL-17 cytokines in stimulated splenocyte cultures, and significant production of antigen-specific sIgA was observed in the colonic tissues of immunized mice. We demonstrated that FnBPA (pValac:) generated a cellular and humoral immune response after oral immunization of mice. The strategy developed in this work may represent an interesting DNA mucosal vaccine candidate against tuberculosis, using the fusion of two highly immunogenic antigens delivered by safe lactic acid bacteria.

摘要

迫切需要开发一种针对结核病的新疫苗策略,并且这一需求得到了全球科学界的大力推动。在这项工作中,我们构建了一种基于两种抗原ESAT-6和Ag85A融合的乳酸球菌DNA疫苗,并检测了其免疫原性。将 和 基因的编码序列融合并克隆到真核表达pValac载体中,并证实了该载体的功能。然后,获得了FnBPA(pValac:)并用于小鼠的口服免疫。该菌株在刺激的脾细胞培养物中诱导IFN-γ、TNF-α和IL-17细胞因子显著增加,并且在免疫小鼠的结肠组织中观察到抗原特异性sIgA的显著产生。我们证明,FnBPA(pValac:)在小鼠口服免疫后产生了细胞免疫和体液免疫反应。这项工作中开发的策略可能代表了一种有趣的针对结核病的DNA粘膜疫苗候选物,它利用安全的乳酸菌递送两种高度免疫原性抗原的融合体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe34/8173160/0ab26229d28e/fmicb-12-676172-g0001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验