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首页> 外文期刊>The journal of immunology >Induction of CD8 T Cells against a Novel Epitope in TB10.4: Correlation with Mycobacterial Virulence and the Presence of a Functional Region of Difference-1
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Induction of CD8 T Cells against a Novel Epitope in TB10.4: Correlation with Mycobacterial Virulence and the Presence of a Functional Region of Difference-1

机译:TB10.4中针对新型抗原决定簇的CD8 T细胞诱导:与分枝杆菌毒力和差分1功能区的存在相关。

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Although infection with Mycobacterium tuberculosis (M.tb) induces a robust CD8 T cell response, the role of CD8 T cells in the defense against M.tb, and the mechanisms behind the induction of CD8 T cells, is still not clear. TB10.4 is a recently described Ag that is expressed by both bacillus Calmette-Guérin (BCG) and M.tb. In the present study, we describe a novel CD8 T cell epitope in TB10.4, TB10.43-11. We show that TB10.43-11-specific CD8 T cells are induced at the onset of infection and are present throughout the infection in high numbers. TB10.43-11 CD8 T cells were recruited to the site of infection and expressed CD44, TNF-α, and IFN-γ. In addition, TB10.43-11 CD8 T cells showed an up-regulation of FasL and LAMP-1/2 (CD107A/B), which correlated with a strong in vivo cytolytic activity. The induction of TB10.43-11-specific CD8 T cells was less pronounced following infection with BCG compared to infection with M.tb. By using a rBCG expressing the genetic region of difference-1 (RD1), we show that the presence of a functional RD1 region increases the induction of TB10.43-11-specific CD8 T cells as well as the bacterial virulence. Finally, as an M.tb variant lacking the genetic region RD1 also induced a significant amount of TB10.43-11-specific CD8 T cells, and exhibited increased virulence compared with BCG, our data suggest that virulence in itself is also involved in generating a robust CD8 T cell response against mycobacterial epitopes, such as TB10.43-11.
机译:尽管结核分枝杆菌(M.tb)感染会诱导强烈的CD8 T细胞反应,但CD8 T细胞在防御M.tb中的作用以及诱导CD8 T细胞的机制尚不清楚。 TB10.4是最近描述的一种抗原,由卡介苗(BCG)和M.tb共同表达。在本研究中,我们描述了TB10.4,TB10.43-11中的新型CD8 T细胞表位。我们显示,TB10.43-11-特异的CD8 T细胞在感染开始时就被诱导,并且在整个感染过程中以大量存在。 TB10.43-11 CD8 T细胞被募集到感染部位并表达CD44,TNF-α和IFN-γ。此外,TB10.43-11 CD8 T细胞显示出FasL和LAMP-1 / 2(CD107A / B)的上调,这与体内强烈的细胞溶解活性相关。与M.tb感染相比,BCG感染后TB10.43-11-特异性CD8 T细胞的诱导作用不明显。通过使用表达差异1(RD1)的遗传区域的rBCG,我们显示功能性RD1区域的存在增加了TB10.43-11-特异性CD8 T细胞的诱导以及细菌毒力。最后,由于缺少遗传区RD1的M.tb变体也诱导了大量TB10.43-11-特异性CD8 T细胞,并且与BCG相比显示出更高的毒力,我们的数据表明,毒力本身也参与了产生针对分枝杆菌抗原决定簇(例如TB10.43-11)的强CD8 T细胞应答。

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