酪氨酸激酶抑制剂伊马替尼通过消耗效应调节性T细胞增强肿瘤免疫

A. Tanaka, H. Nishikawa, Shinsuke Noguchi, D. Sugiyama, Hiromasa Morikawa, Yoshiko Takeuchi, D. Ha, Naoya Shigeta, T. Kitawaki, Y. Maeda, Takuro Saito, Yoshinori Shinohara, Y. Kameoka, K. Iwaisako, F. Monma, K. Ohishi, J. Karbach, E. Jäger, K. Sawada, N. Katayama, N. Takahashi, S. Sakaguchi
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引用次数: 58

摘要

作为一种新型的抗癌试剂,伊马替尼不仅可以抑制BCR-ABL致癌蛋白,还可以作为脱靶抑制T细胞中的LCK,能够选择性地消耗成熟T细胞,从而引起对各种癌症的有效免疫反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tyrosine kinase inhibitor imatinib augments tumor immunity by depleting effector regulatory T cells
As a novel type of anticancer reagent, imatinib inhibits not only BCR-ABL oncogenic protein but also LCK in T cells as an off-target, being able to selectively deplete mature T reg cells and thereby evoke effective immune responses to various cancers.
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