首页> 外文期刊>APMIS: Acta Pathologica, Microbiologica et Immunologica Scandinavica >Liposomes or traditional adjuvants: induction of bactericidal activity by the macrophage infectivity potentiator protein (Mip) of Neisseria meningitidis
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Liposomes or traditional adjuvants: induction of bactericidal activity by the macrophage infectivity potentiator protein (Mip) of Neisseria meningitidis

机译:脂质体或传统佐剂:巨噬细胞感染率蛋白(MIP)诱导杀菌剂的杀菌活性

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摘要

Currently, one of the main approaches to achieve a vaccine for serogroup B Neisseria meningitidis is based on outer membrane proteins with low antigenic variability among strains. Since these proteins tend to be minor components of the outer membrane, recombinant production is required to obtain them in sufficient amounts for evaluation and development of vaccines. In this study, we analysed the ability of recombinant macrophage infectivity potentiator (rMip) protein to induce protective bactericidal activity in mice. The rMip protein was cloned from N.meningitidis strain H44/76 and was used to immunise mice, and the sera obtained were tested against the homologous and several heterologous N.meningitidis strains. The sera were obtained using the rMip alone, with adjuvant Al(OH)(3), or after inclusion into liposomes. Bactericidal activity was variable depending on the strain, although high titres were seen against strains H44/76 and NmP27. Liposomes enhanced fourfold the reactivity against the homologous strain. The results presented suggest that the rMip protein should be considered a promising candidate for the improvement of future protein-based vaccines.
机译:目前,实现Serogroup B Neisseria Meningitidis疫苗的主要方法之一是基于外膜蛋白,菌株之间的抗原变异性低。由于这些蛋白质倾向于是外膜的少量组分,因此需要重组生产来获得足够的量进行评估和发育疫苗的量。在这项研究中,我们分析了重组巨噬细胞感染性增强剂(RMIP)蛋白在小鼠中诱导保护性杀菌活性的能力。从N.Meningitidis菌株H44 / 76克隆rmip蛋白,用来免疫小鼠,并将获得的血清与同源物和几种异源N.Meningitidis菌株进行测试。单独使用rmip获得血清,用佐剂Al(OH)(3),或在包入脂质体之后。取决于菌株的杀菌活性是可变的,尽管对菌株H44 / 76和NMP27观察到高滴度。脂质体增强了对同源菌株的反应性的四倍。提出的结果表明,RMIP蛋白应被视为改善未来蛋白质疫苗的有希望的候选者。

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