细胞毒性
细胞毒性T细胞
体内
离体
细胞
癌细胞
生物
细胞凋亡
癌症研究
药理学
行动方式
癌症
毒性
体外
医学
遗传学
内科学
毒理
生物化学
生物技术
作者
Claire Vennin,Chiara M. Cattaneo,Leontien Bosch,Serena Vegna,Xuhui Ma,Hugo G.J. Damstra,Moreno Martinovic,Efi Tsouri,Mila Ilić,Leyla Azarang,Jan R.T. van Weering,Emilia M. Pulver,Amber L. Zeeman,Tim Schelfhorst,Jeroen Lohuis,Anne C. Rios,Johanna F. Dekkers,Leila Akkari,Renée X. de Menezes,René H. Medema
出处
期刊:Cancer Cell
[Elsevier]
日期:2023-06-01
卷期号:41 (6): 1170-1185.e12
被引量:35
标识
DOI:10.1016/j.ccell.2023.05.009
摘要
Although treatment with taxanes does not always lead to clinical benefit, all patients are at risk of their detrimental side effects such as peripheral neuropathy. Understanding the in vivo mode of action of taxanes can help design improved treatment regimens. Here, we demonstrate that in vivo, taxanes directly trigger T cells to selectively kill cancer cells in a non-canonical, T cell receptor-independent manner. Mechanistically, taxanes induce T cells to release cytotoxic extracellular vesicles, which lead to apoptosis specifically in tumor cells while leaving healthy epithelial cells intact. We exploit these findings to develop an effective therapeutic approach, based on transfer of T cells pre-treated with taxanes ex vivo, thereby avoiding toxicity of systemic treatment. Our study reveals a different in vivo mode of action of one of the most commonly used chemotherapies, and opens avenues to harness T cell-dependent anti-tumor effects of taxanes while avoiding systemic toxicity.
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