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Additive and Synergistic Bactericidal Activity of Antibodies Directed against Minor Outer Membrane Proteins of Neisseria meningitidis

机译:针对脑膜炎奈瑟氏球菌外膜蛋白的抗体的累加和协同杀菌活性

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Neisseria meningitidis serogroup B is a major cause of bacterial meningitis in younger populations. The available vaccines are based on outer membrane vesicles obtained from wild-type strains. In children less than 2 years old they confer protection only against strains expressing homologous PorA, a major, variable outer membrane protein (OMP). We genetically modified a strain in order to eliminate PorA and to overproduce one or several minor and conserved OMPs. Using a mouse model mimicking children's PorA-specific bactericidal activity, it was demonstrated that overproduction of more than one minor OMP is required to elicit antibodies able to induce complement-mediated killing of strains expressing heterologous PorA. It is concluded that a critical density of bactericidal antibodies needs to be reached at the surface of meningococci to induce complement-mediated killing. With minor OMPs, this threshold is reached when more than one antigen is targeted, and this allows cross-protection.
机译:B型脑膜炎奈瑟氏球菌是年轻人群细菌性脑膜炎的主要原因。可用的疫苗基于从野生型菌株获得的外膜囊泡。在不到2岁的儿童中,它们仅针对表达同源PorA(一种主要的可变外膜蛋白(OMP))的菌株提供保护。我们对菌株进行了基因改造,以消除PorA并过量生产一种或几种次要且保守的OMP。使用模仿儿童的PorA特异性杀菌活性的小鼠模型,已证明需要过量生产一种以上的次要OMP才能引发能够诱导补体介导的表达异源PorA的菌株杀死的抗体。结论是,需要在脑膜炎球菌表面达到临界的杀菌抗体密度才能诱导补体介导的杀伤。对于次要的OMP,当靶向一种以上的抗原时,将达到此阈值,从而可以进行交叉保护。

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