蛋白质和DNA纳米粒抗幽门螺杆菌多抗原疫苗:体内评价

L. Figueiredo, C. Calado, A. Almeida, L. Gonçalves
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引用次数: 4

摘要

针对幽门螺杆菌的免疫接种是抗生素耐药性和再感染情况的一个有吸引力的选择。尽管如此,菌株的遗传异质性、蛋白抗原和DNA的低免疫原性仍然是这种方法的障碍。基于致病相关性,我们开发了多基因幽门螺杆菌dna纳米颗粒和蛋白质纳米颗粒疫苗。选择CagA、VacA、HpaA、UreB、HomB和GroEL 6种抗原构建疫苗。制备了CS/DS和CS/Alg /TPP纳米颗粒与DNA和嵌合蛋白的不同组合作为疫苗体系。对BALB/c小鼠进行体外免疫和口服免疫后的免疫应答进行评价。口服疫苗成功地刺激了粘膜免疫,而免疫有效地引发了更平衡的细胞/体液免疫反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protein and DNA nanoparticulate multiantigenic vaccines against H. pylori: In vivo evaluation
Immunisation against H. pylori is an attractive option for antibiotic resistance and reinfection situations. Strain genetic heterogeneity, and low immunogenicity of protein antigens and DNA alone are nonetheless obstacles to this approach. We developed multigenic H. pylori DNA-nanoparticle and protein-nanoparticle vaccines based on pathogenic relevance. Six antigens were chosen for the vaccine construction: CagA, VacA, HpaA, UreB, HomB and GroEL. Different combinations of CS/DS and CS/Alg /TPP nanoparticles with DNA and chimeric proteins were produced as vaccine systems. Immune responses were evaluated after i.m. and oral immunisation of BALB/c mice. Oral vaccination successfully stimulated mucosal immunity while i.m. immunisation efficiently elicited a more equilibrated cellular/humoral immune response.
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