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诱导针对TB10.4中一个新表位的CD8 T细胞:与分枝杆菌毒力及差异-1功能区存在的相关性

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.

作者信息

Billeskov Rolf, Vingsbo-Lundberg Carina, Andersen Peter, Dietrich Jes

机构信息

Department of Infectious Disease Immunology, Statens Serum Institut, Copenhagen, Denmark.

出版信息

J Immunol. 2007 Sep 15;179(6):3973-81. doi: 10.4049/jimmunol.179.6.3973.

Abstract

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, TB10.4(3-11). We show that TB10.4(3-11)-specific CD8 T cells are induced at the onset of infection and are present throughout the infection in high numbers. TB10.4(3-11) CD8 T cells were recruited to the site of infection and expressed CD44, TNF-alpha, and IFN-gamma. In addition, TB10.4(3-11) 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 TB10.4(3-11)-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 TB10.4(3-11)-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 TB10.4(3-11)-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 TB10.4(3-11).

摘要

尽管结核分枝杆菌(M.tb)感染可诱导强烈的CD8 T细胞反应,但CD8 T细胞在抗M.tb防御中的作用以及CD8 T细胞诱导背后的机制仍不清楚。TB10.4是一种最近描述的抗原,卡介苗(BCG)和M.tb均表达该抗原。在本研究中,我们描述了TB10.4中一个新的CD8 T细胞表位,即TB10.4(3 - 11)。我们发现,TB10.4(3 - 11)特异性CD8 T细胞在感染开始时被诱导产生,并且在整个感染过程中大量存在。TB10.4(3 - 11) CD8 T细胞被募集到感染部位,并表达CD44、肿瘤坏死因子-α(TNF-α)和干扰素-γ(IFN-γ)。此外,TB10.4(3 - 11) CD8 T细胞显示FasL和溶酶体相关膜蛋白-1/2(LAMP-1/2,即CD107A/B)上调,这与强大 的体内细胞溶解活性相关。与M.tb感染相比,BCG感染后TB10.4(3 - 11)特异性CD8 T细胞的诱导不太明显。通过使用表达差异区域-1(RD1)基因区域的重组卡介苗(rBCG),我们发现功能性RD1区域的存在增加了TB10.4(3 - 11)特异性CD8 T细胞的诱导以及细菌毒力。最后,由于一种缺乏RD1基因区域的M.tb变体也诱导产生了大量的TB10.4(3 - 11)特异性CD8 T细胞,并且与BCG相比表现出增加的毒力,我们的数据表明毒力本身也参与产生针对分枝杆菌表位(如TB10.4(3 - 11))的强大CD8 T细胞反应。

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