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首页> 外文期刊>Scandinavian journal of immunology. >MF59 adjuvant enhances the immunogenicity and protective immunity of the OmpK/Omp22 fusion protein from Acineterbacter baumannii Acineterbacter baumannii through intratracheal inoculation in mice
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MF59 adjuvant enhances the immunogenicity and protective immunity of the OmpK/Omp22 fusion protein from Acineterbacter baumannii Acineterbacter baumannii through intratracheal inoculation in mice

机译:MF59佐剂通过小鼠肿瘤内接种,增强了来自acineterbacterbaumannii acineterbacterbacterbacterbacterbacterbacterbacterbacterbacterbacterbaction的免疫原性和保护性免疫蛋白

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Abstract Acinetobacter baumannii ( A baumannii ) is an emerging nosocomial pathogenic bacterium which leads to hospital infections. The increase in drug‐resistant A baumannii strains makes it difficult to control by using common antibiotics. The development of effective vaccines is an alternative means to avoid A baumannii infections. In the present study, Balb/c mice were inoculated intratracheally with 30?μg of OmpK/Omp22 fusion protein alone or OmpK/Omp22 formulated with MF59 adjuvant. After two times of boosting at day 14 and 21, the antigen‐specific antibody levels and the protective immunity against A baumannii challenge were evaluated. The results showed that the OmpK/Omp22 formulated with MF59 immunized mice produced much higher level of antigen‐specific antibodies compared to mice immunized with OmpK/Omp22 alone ( P? ?0.01). Mice immunized with 30?μg of OmpK/Omp22 formulated with MF59 also provided more potent protection post‐challenge, which showed lower bacterial loads in the blood and lung tissue, lower level of blood inflammatory cytokines and higher survival rate (83.3%) than mice immunized with OmpK/Omp22 alone ( P?? 0.001). In conclusion, this study demonstrated that OmpK/Omp22 fusion protein adjuvanted with MF59 induced superior immune response and better protection than OmpK/Omp22 alone through intratracheal inoculation in mice .
机译:摘要AcineTobacter Baumannii(Baumannii)是一种新兴的医院致病细菌,导致医院感染。耐药性增加Baumannii菌株使得难以使用普通抗生素来控制。有效疫苗的发展是一种替代方法,以避免Baumannii感染。在本研究中,用30μgμgOMPK / OMP22融合蛋白或用MF59佐剂配制的OMPK / OMP22接种Balb / C小鼠。在第14天和第21天提高两次后,评估抗原特异性抗体水平和对Baumannii挑战的保护性免疫。结果表明,与单独用OMPK / OMP22免疫的小鼠相比,用MF59免疫小鼠配制的OMPK / OMP22产生了更高水平的抗原特异性抗体(P = 0.01)。用MF59配制的30μgMompk/ OMP22免疫的小鼠还提供了更有效的保护后攻击后,这表明血液和肺组织中的细菌载荷较低,血液炎症细胞因子较低,存活率较高(83.3%)比小鼠更高单独用OMPK / OMP22免疫(P?<0.001)。总之,本研究证明,OMPK / OMP22融合蛋白辅助MF59诱导优异的免疫应答,并通过小鼠肿瘤内接种单独服用优异的免疫应答和更好的保护。

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