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首页> 外文期刊>Vaccine >Identification of HLA-DR4-restricted T-cell epitope on MPT51 protein, a major secreted protein derived from Mycobacterium tuberculosis using MPT51 overlapping peptides screening and DNA vaccination.
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Identification of HLA-DR4-restricted T-cell epitope on MPT51 protein, a major secreted protein derived from Mycobacterium tuberculosis using MPT51 overlapping peptides screening and DNA vaccination.

机译:使用MPT51重叠肽段筛选和DNA疫苗接种,鉴定MPT51蛋白上的HLA-DR4限制性T细胞表位,MPT51是结核分枝杆菌的主要分泌蛋白。

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摘要

We identified a novel HLA-DR4-restricted CD4+ T-cell epitope on a secreted antigen of Mycobacterium tuberculosis, MPT51, in 004149-MM HLA-DR4-transgenic mice which express HLA-DRB1*0401, but not murine MHC class II molecules. The mice were immunized with plasmid DNA encoding MPT51 using gene gun and interferon (IFN)- gamma production from the immune splenocytes was analyzed. In response to overlapping synthetic peptides covering the mature MPT51 sequence, only one peptide, p191-210, stimulated the splenocytes to produce IFN- gamma . Further analysis using flow cytometry and computer-assisted algorithm, ProPred, narrowed down the region of CD4+ T-cell epitope to p191-202. The CD4+ T-cell epitope would be feasible for vaccine design against tuberculosis as well as for analysis of MPT51-specific T-cells in M. tuberculosis infection.
机译:我们在表达HLA-DRB1 * 0401的004149-MM HLA-DR4-转基因小鼠中鉴定了结核分枝杆菌MPT51分泌抗原上的一种新型HLA-DR4限制性CD4 + T细胞表位。不是鼠类MHC II类分子。使用基因枪用编码MPT51的质粒DNA免疫小鼠,并分析免疫脾细胞中干扰素(IFN)-γ的产生。对于覆盖成熟MPT51序列的重叠合成肽,只有一种肽p191-210刺激脾细胞产生IFN-γ。使用流式细胞仪和计算机辅助算法ProPred进行的进一步分析将CD4 + T细胞表位的区域缩小到p191-202。 CD4 + T细胞表位对于设计抗结核疫苗以及分析M中MPT51特异性T细胞将是可行的。结核感染。

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