首页> 外文期刊>Trends in cancer. >Resisting T cell attack: tumor-cell-intrinsic defense and reparation mechanisms
【24h】

Resisting T cell attack: tumor-cell-intrinsic defense and reparation mechanisms

机译:抵抗T细胞攻击:肿瘤-细胞-内在防御和修复机制

获取原文
获取原文并翻译 | 示例
           

摘要

Cytotoxic T lymphocytes (CTLs) are antigen-specific killer cells equipped to identify and eliminate host cells that have been altered through infection or transformation. Both chimeric antigen-receptor (CAR) T cell therapies and immune checkpoint blockade (ICB) therapies are based on successful elimination of tumor cells by cytotoxic effectors. In this opinion article, we outline cell-intrinsic mechanisms by which tumor cells defend against CTLs, highlighting pathways that confer resistance and proposing opportunities for combination therapies. We discuss how exogenous killing entities [e.g., supramolecular attack particles (SMAPs)] offer a novel strategy to circumvent cellular resistance mechanisms. Our opinion article highlights the importance of identifying, quantifying, and targeting tumor defense mechanisms at the interface between tumor cells and CTLs as a critical consideration in the development of immunotherapy approaches.
机译:细胞毒性T淋巴细胞(ctl)细胞杀伤能力识别和消除宿主细胞通过改变感染或转换。嵌合抗原受体(汽车)T细胞疗法和免疫检查点封锁(ICB)疗法是基于成功的消除肿瘤细胞通过细胞毒性效应物。篇文章中,我们概述细胞内在机制肿瘤细胞抵御ctl,强调通路产生耐药性提出结合的机会疗法。实体(例如,超分子攻击粒子(smap)]提供了一个新策略来规避细胞的耐药机制。文章强调了识别的重要性,量化,针对肿瘤的防御机制在肿瘤细胞之间的接口和ctl作为重要考虑的免疫治疗方法的发展。

著录项

相似文献

  • 外文文献
  • 中文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号