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对分泌型p60抗原具有特异性的CD8 T淋巴细胞可预防单核细胞增生李斯特菌感染。

CD8 T lymphocytes specific for the secreted p60 antigen protect against Listeria monocytogenes infection.

作者信息

Harty J T, Pamer E G

机构信息

Department of Microbiology, College of Medicine, University of Iowa, Iowa City 52242, USA.

出版信息

J Immunol. 1995 May 1;154(9):4642-50.

PMID:7722316
Abstract

The ability of Listeria monocytogenes to gain access to the cytoplasm of infected cells results in the processing and presentation of bacterial Ags through the MHC class I pathway. As a result, CD8 T cells are the most effective mediators of acquired immunity in the mouse model of L. monocytogenes infection. CD8 T cells specific for a single nonamer epitope derived from the secreted virulence factor listeriolysin O (LLO) can protect H-2d mice against lethal infection. Bacteria lacking LLO are avirulent and do not elicit protective immunity in mice. Thus, the failure of LLO minus L. monocytogenes to elicit protective immunity could be caused either by their inability to enter the cytoplasm or to the lack of LLO-derived peptide epitopes. In this report we provide evidence that H-2d restricted CD8 T cells with specificity for another L. monocytogenes protein, the secreted p60 molecule, can protect against infection. Our studies further demonstrate that LLO-dependent induction of protective immunity results from access of the bacterium to the cytoplasm. In addition, these studies provide support for the hypothesis that secreted bacterial proteins are the most important targets for protective CD8 T cell-mediated immunity.

摘要

单核细胞增生李斯特菌进入受感染细胞胞质的能力,导致细菌抗原通过MHC I类途径进行加工和呈递。因此,在单核细胞增生李斯特菌感染的小鼠模型中,CD8 T细胞是获得性免疫最有效的介质。对源自分泌型毒力因子李斯特菌溶血素O(LLO)的单个九聚体表位具有特异性的CD8 T细胞,可以保护H-2d小鼠免受致死性感染。缺乏LLO的细菌无毒力,不会在小鼠中引发保护性免疫。因此,缺失LLO的单核细胞增生李斯特菌无法引发保护性免疫,可能是由于它们无法进入胞质,或者缺乏LLO衍生的肽表位。在本报告中,我们提供证据表明,对另一种单核细胞增生李斯特菌蛋白(分泌型p60分子)具有特异性的H-2d限制性CD8 T细胞可以预防感染。我们的研究进一步证明,依赖LLO的保护性免疫诱导是由于细菌进入胞质所致。此外,这些研究为以下假设提供了支持,即分泌型细菌蛋白是保护性CD8 T细胞介导免疫的最重要靶点。

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