首页> 美国卫生研究院文献>other >Chloroform-Methanol Residue of Coxiella burnetii Markedly Potentiated the Specific Immunoprotection Elicited by a Recombinant Protein Fragment rOmpB-4 Derived from Outer Membrane Protein B of Rickettsia rickettsii in C3H/HeN Mice
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Chloroform-Methanol Residue of Coxiella burnetii Markedly Potentiated the Specific Immunoprotection Elicited by a Recombinant Protein Fragment rOmpB-4 Derived from Outer Membrane Protein B of Rickettsia rickettsii in C3H/HeN Mice

机译:克氏杆菌的氯仿-甲醇残留显着增强了立克次氏体立克次氏体外膜蛋白B衍生的重组蛋白片段rOmpB-4在C3H / HeN小鼠中的特异性免疫保护作用。

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摘要

The obligate intracellular bacteria, Rickettsia rickettsii and Coxiella burnetii, are the potential agents of bio-warfare/bio-terrorism. Here C3H/HeN mice were immunized with a recombinant protein fragment rOmp-4 derived from outer membrane protein B, a major protective antigen of R. rickettsii, combined with chloroform-methanol residue (CMR) extracted from phase I C. burnetii organisms, a safer Q fever vaccine. These immunized mice had significantly higher levels of IgG1 and IgG2a to rOmpB-4 and interferon-γ (IFN-γ) and tumor necrosis factor-α (TNF-α), two crucial cytokines in resisting intracellular bacterial infection, as well as significantly lower rickettsial loads and slighter pathological lesions in organs after challenge with R. rickettsii, compared with mice immunized with rOmpB-4 or CMR alone. Additionally, after challenge with C. burnetii, the coxiella loads in the organs of these mice were significantly lower than those of mice immunized with rOmpB-4 alone. Our results prove that CMR could markedly potentiate enhance the rOmpB-4-specific immunoprotection by promoting specific and non-specific immunoresponses and the immunization with the protective antigen of R. rickettsii combined with CMR of C. burnetii could confer effective protection against infection of R. rickettsii or C. burnetii.
机译:专性细胞内细菌立克次氏菌和伯氏柯立氏菌是生物战/生物恐怖主义的潜在病原体。在这里,C3H / HeN小鼠用重组蛋白片段rOmp-4免疫,该重组蛋白片段来源于外膜蛋白B(里氏乳杆菌的主要保护性抗原),并结合了从阶段I. Burnetii生物体中提取的氯仿-甲醇残留物(CMR)。更安全的Q型发烧疫苗。这些免疫小鼠的rOmpB-4和IFN-γ(IFN-γ)和肿瘤坏死因子-α(TNF-α)是抵抗细胞内细菌感染的两种重要细胞因子,其IgG1和IgG2a的水平明显较高,而其水平则明显较低。与仅用rOmpB-4或CMR免疫的小鼠相比,用立克次氏杆菌刺激后的器官中的立克次氏体负荷和轻微的病理病变。另外,用伯氏梭菌攻击后,这些小鼠器官中的coxiella含量显着低于单独用rOmpB-4免疫的小鼠。我们的结果证明,CMR可通过促进特异性和非特异性免疫反应来显着增强rOmpB-4特异性免疫保护,而用立克次氏菌的保护性抗原与伯氏梭状芽胞杆菌的CMR结合进行免疫可赋予针对R感染的有效保护rickettsii或 C burnetii

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