细胞毒性T细胞
CD8型
金黄色葡萄球菌
皮肤T细胞淋巴瘤
免疫学
癌症研究
T细胞
医学
癌症
淋巴瘤
免疫系统
生物
蕈样真菌病
体外
内科学
生物化学
遗传学
细菌
作者
Edda Blümel,Shamaila Munir Ahmad,Claudia Nastasi,Andreas Willerslev-Olsen,Maria Gluud,Simon Fredholm,Tengpeng Hu,Bas G. J. Surewaard,Lise M. Lindahl,H Fogh,Sergei B. Koralov,Lise Mette Rahbek Gjerdrum,Rachael A. Clark,Lars Iversen,Thorbjørn Krejsgaard,Charlotte M. Bonefeld,Carsten Geisler,Jürgen C. Becker,Anders Woetmann,Mads Hald Andersen
出处
期刊:OncoImmunology
[Landes Bioscience]
日期:2020-01-01
卷期号:9 (1): 1751561-1751561
被引量:35
标识
DOI:10.1080/2162402x.2020.1751561
摘要
Staphylococcus aureus and its toxins have been linked to disease progression and mortality in advanced stages of cutaneous T-cell lymphoma (CTCL). CD8+ T cells play a crucial role in anti-cancer responses and high CD8+ T cell numbers in tumor lesions are associated with a favorable prognosis in CTCL. Here, we show that CD8+ T cells from both healthy donors and Sézary syndrome patients are highly susceptible to cell death induced by Staphylococcal alpha-toxin, whereas malignant T cells are not. Importantly, alpha-toxin almost completely blocks cytotoxic killing of CTCL tumor cells by peptide-specific CD8+ T cells, leading to their escape from induced cell death and continued proliferation. These findings suggest that alpha-toxin may favor the persistence of malignant CTCL cells in vivo by inhibiting CD8+ T cell cytotoxicity. Thus, we propose a novel mechanism by which colonization with Staphylococcus aureus may contribute to cancer immune evasion and disease progression in CTCL.
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