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Immunization with the Recombinant PorB Outer Membrane Protein Induces a Bactericidal Immune Response against Neisseria meningitidis

机译:用重组PorB外膜蛋白免疫可诱导针对脑膜炎奈瑟氏菌的杀菌免疫反应。

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摘要

Infections with Neisseria meningitidis are characterized by life-threatening meningitis and septicemia. The meningococcal porin proteins from serogroup B meningococci have been identified as candidates for inclusion in vaccines to prevent such infections. In this study, we investigated the vaccine potential of the PorB porin protein free of other meningococcal components. The porB gene from a strain of Neisseria meningitidis expressing the class 3 outer membrane porin protein (PorB3) was cloned into the pRSETB vector, and the protein was expressed at high levels in a heterologous host Escherichia coli. The recombinant protein was purified to homogeneity by affinity chromatography and used for immunization after incorporation into liposomes and into micelles composed either of zwitterionic detergent or nondetergent sulfobetaine. The immunogenicity of these preparations was compared to recombinant PorB protein adsorbed to Al(OH)3 adjuvant as a control. Although sera raised against the protein adsorbed to Al(OH)3 reacted with the purified recombinant protein, sera raised against liposomes and micelles showed greater activity with native protein, as measured by enzyme immunoassay with outer membranes and by whole-cell immunofluorescence. Reactivity with native protein was considerably enhanced by incorporation of the adjuvant monophosphoryl lipid A into the liposome or micelle preparations. Recognition of the native protein was in a serotype-specific manner and was associated with the ability of the antisera to promote high levels of serotype-specific complement-mediated killing of meningococci. These results demonstrate that the PorB protein should be considered as a component of a vaccine designed to prevent serogroup B meningococcal infection.
机译:脑膜炎奈瑟氏菌感染的特征是威胁生命的脑膜炎和败血病。来自血清群B脑膜炎球菌的脑膜炎球菌孔蛋白已被鉴定为可用于预防此类感染的疫苗。在这项研究中,我们调查了不含其他脑膜炎球菌成分的PorB孔蛋白的疫苗潜力。将表达3类外膜孔蛋白(PorB3)的脑膜炎奈瑟氏菌菌株的porB基因克隆到pRSETB载体中,并在异源宿主大肠杆菌中高水平表达该蛋白。通过亲和色谱将重组蛋白纯化至均质,并在掺入脂质体和由两性离子去污剂或非去污剂磺基甜菜碱组成的胶束中用于免疫。将这些制剂的免疫原性与吸附在Al(OH)3佐剂上的重组PorB蛋白作对照。尽管针对吸附在Al(OH)3上的蛋白质产生的血清与纯化的重组蛋白发生了反应,但是针对脂质体和微团的血清显示出对天然蛋白质的更大活性,这是通过外膜酶免疫测定和全细胞免疫荧光测定的。通过将佐剂单磷酰基脂质A掺入脂质体或胶束制剂中,与天然蛋白质的反应性大大提高。天然蛋白的识别是以血清型特异性的方式进行的,并且与抗血清促进高水平血清型特异性补体介导的脑膜炎球菌杀死的能力有关。这些结果表明,应将PorB蛋白视为旨在预防B血清群脑膜炎球菌感染的疫苗的组成部分。

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