Michaelsen T E, Aase A, Kolberg J, Wedge E, Rosenqvist E
Department of Vaccinology, National Institute of Public Health, P.O. Box 4404 Torshov, 0403, Oslo, Norway.
Vaccine. 2001 Jan 8;19(11-12):1526-33. doi: 10.1016/s0264-410x(00)00324-8.
It is reported here that the PorB3 porin proteins of serotype 4 and 15 are poorly accessible for antibody binding on live Neisseria meningitidis bacteria, whereas the allelic PorB2 and the PorA outer membrane protein appear to be highly accessible. This was revealed by flow cytometry analysis using several mouse monoclonal antibodies (mAbs) as well as PorB3 specific antibodies isolated from post vaccination and patient sera. However, strong antibody binding to the PorB3 protein was observed after killing the bacteria with ethanol. The reason for the lack of epitope exposure could be a shielding effect of the carbohydrate chains of lipopolysaccharides (LPS) possibly combined with short extra-cellular loops in the PorB3 protein. The findings indicate that the PorB3 protein is not an optimal target for protective antibodies induced by vaccination.
据报道,血清型4和15的PorB3孔蛋白在活的脑膜炎奈瑟氏菌上难以与抗体结合,而等位基因PorB2和PorA外膜蛋白似乎极易与抗体结合。这是通过使用几种小鼠单克隆抗体(mAb)以及从疫苗接种后和患者血清中分离出的PorB3特异性抗体进行流式细胞术分析揭示的。然而,在用乙醇杀死细菌后,观察到抗体与PorB3蛋白有强烈结合。表位暴露缺乏的原因可能是脂多糖(LPS)糖链的屏蔽作用,可能与PorB3蛋白中的短细胞外环相结合。这些发现表明,PorB3蛋白不是疫苗诱导的保护性抗体的最佳靶点。