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经单核细胞增生李斯特菌溶血素处理的抗原呈递细胞对抗原特异性T细胞受体的拮抗作用:一种新型免疫逃逸机制

Antigen-specific T cell receptor antagonism by antigen-presenting cells treated with the hemolysin of Listeria monocytogenes: a novel type of immune escape.

作者信息

Darji A, Stockinger B, Wehland J, Chakraborty T, Weiss S

机构信息

Division of Cell Biology and Immunology, National Research Centre for Biotechnology, Braunschweig, Germany. ada@gbf-braunschweig-de

出版信息

Eur J Immunol. 1997 Jul;27(7):1696-703. doi: 10.1002/eji.1830270716.

Abstract

We have examined the influence of listeriolysin O (LLO), the hemolysin secreted by the pathogenic bacterium Listeria monocytogenes, on major histocompatibility complex class II-dependent T cell activation. Stimulation of T cells by native antigens but not by peptides is inhibited upon pretreatment of antigen-presenting cells (APC) with LLO. Experiments presented here reveal that this inhibition is not due to a lack in processing of antigen by APC but is the result of an irreversible inactivation of T cells that recognize antigen on LLO-treated APC. Incubation of mixtures of two different T cells where only one antigen was presented on LLO-treated APC suggested that T cell inactivation is antigen specific. The inactivation was dominant and could be observed even in the presence of amounts of synthetic peptides that normally lead to T cell responses. This condition is reminiscent of the T cell inhibition observed when antagonistic and stimulatory peptides are added to APC at the same time. Our results thus reveal a novel type of interference by pathogens with antigen presentation and T cell stimulation that could give the pathogen a decisive advantage in dissemination and disease.

摘要

我们研究了致病性细菌单核细胞增生李斯特菌分泌的溶血素——李斯特菌溶素O(LLO)对主要组织相容性复合体II类依赖性T细胞活化的影响。在用LLO预处理抗原呈递细胞(APC)后,天然抗原而非肽对T细胞的刺激受到抑制。本文所展示的实验表明,这种抑制并非由于APC对抗原的加工不足,而是识别LLO处理的APC上抗原的T细胞发生不可逆失活的结果。在两种不同T细胞的混合物中,只有一种抗原呈现在LLO处理的APC上,培养结果表明T细胞失活具有抗原特异性。这种失活具有主导性,即使存在通常能引发T细胞反应的合成肽量时也能观察到。这种情况类似于同时向APC添加拮抗肽和刺激肽时观察到的T细胞抑制。因此,我们的结果揭示了病原体对抗原呈递和T细胞刺激的一种新型干扰,这可能使病原体在传播和疾病发生中获得决定性优势。

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