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首页> 外文期刊>Proteomics >Immunodominant Francisella tularensis antigens identified using proteome microarray. Crown Copyright 2007 Dstl.
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Immunodominant Francisella tularensis antigens identified using proteome microarray. Crown Copyright 2007 Dstl.

机译:使用蛋白质组微阵列鉴定了免疫性土拉弗朗西斯菌抗原。 Crown版权所有2007 Dstl。

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摘要

Stimulation of protective immune responses against intracellular pathogens is difficult to achieve using non-replicating vaccines. BALB/c mice immunized by intramuscular injection with killed Francisella tularensis (live vaccine strain) adjuvanted with preformed immune stimulating complexes admixed with CpG, were protected when systemically challenged with a highly virulent strain of F. tularensis (Schu S4). Serum from immunized mice was used to probe a whole proteome microarray in order to identify immunodominant antigens. Eleven out of the top 12 immunodominant antigens have been previously described as immunoreactive in F. tularensis. However, 31 previously unreported immunoreactive antigens were revealed using this approach. Twenty four (50%) of the ORFs on the immunodominant hit list belonged to the category of surface or membrane associated proteins compared to only 22% of the entire proteome. There were eight hypothetical protein hits and eight hits from proteins associated with different aspects of metabolism. The chip also allowed us to readily determine the IgG subclass bias, towards individual or multiple antigens, in protected and unprotected animals. These data give insight into the protective immune response and have potentially important implications for the rational design of non-living vaccines for tularemia and other intracellular pathogens.
机译:使用非复制型疫苗很难刺激针对细胞内病原体的保护性免疫应答。当肌肉内注射高毒性F. tularensis菌株(Schu S4)时,通过肌肉注射灭活的弗朗西斯菌(活疫苗株)和预先混合的CpG的免疫刺激复合物免疫的BALB / c小鼠受到保护。来自免疫小鼠的血清用于探测整个蛋白质组微阵列,以鉴定免疫优势抗原。先前已经描述了前12种免疫显性抗原中的11种在T.tularensis中具有免疫反应性。但是,使用这种方法发现了31种以前未报告的免疫反应性抗原。免疫显性命中清单上的ORF中有二十四(50%)个属于表面或膜相关蛋白,而整个蛋白质组中只有22%。有八种假设的蛋白质命中值,八种来自与代谢不同方面相关的蛋白质的命中值。该芯片还使我们能够轻松确定受保护和不受保护的动物中针对单个或多个抗原的IgG亚类偏倚。这些数据可洞悉保护性免疫反应,并可能对tularemia和其他细胞内病原体的无生命疫苗的合理设计产生重要影响。

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