CAR-NK 细胞中 IL-10 的耗竭增强肿瘤微环境的重编程并改善治疗效果
Depletion of IL-10 in CAR-NK cells augments reprogramming of the tumor microenvironment and ameliorates therapeutic efficacy.
我们的研究结果表明,抑制IL-10分泌可增强CAR工程化NK-92细胞的治疗潜力,提示这一策略有望成为临床转化的有前景途径。
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Depletion of IL-10 in CAR-NK cells augments reprogramming of the tumor microenvironment and ameliorates therapeutic efficacy.
我们的研究结果表明,抑制IL-10分泌可增强CAR工程化NK-92细胞的治疗潜力,提示这一策略有望成为临床转化的有前景途径。
ErbB2/HER2-targeted CAR-NK cells eliminate breast cancer cells in an organoid model that recapitulates tumor progression.
嵌合抗原受体工程化 NK 细胞在过继性肿瘤免疫治疗中展现出前景。
Intracranial injection of natural killer cells engineered with a HER2-targeted chimeric antigen receptor in patients with recurrent glioblastoma.
颅内注射HER2靶向CAR-NK细胞在复发性GB患者中是可行且安全的。1 108个NK-92/5.28.z细胞被确定为后续扩展队列重复局部注射CAR-NK细胞的最大可行剂量。
Locoregional and systemic adoptive cellular therapies for pediatric brain tumors: a systematic review of CAR‑T, TCR‑engineered T cells, and NK cell st
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CAR-NK cell therapy combined with checkpoint inhibition induces an NKT cell response in glioblastoma.
该联合治疗逆转了免疫抑制性肿瘤微环境,T 细胞和 NKT 细胞浸润增加。
Prospective Molecular Targets for Natural Killer Cell Immunotherapy against Glioblastoma Multiforme.
多形性胶质母细胞瘤(GBM)是最常见的原发性恶性脑肿瘤类型,总生存率极低。
AAV-mediated gene transfer of a checkpoint inhibitor in combination with HER2-targeted CAR-NK cells as experimental therapy for glioblastoma.
局部使用编码aPD-1的HER2-AAVs联合抗HER2.CAR/NK-92细胞治疗,可能是GB免疫治疗的一种有前景的新策略,具有增强疗效并减少免疫检查点抑制剂全身副作用的潜力。
A Bibliometric and Knowledge-Map Analysis of CAR-T Cells From 2009 to 2021.
作为一种具有巨大潜力和临床应用前景的抗肿瘤疗法,CAR-T细胞疗法仍处于快速发展阶段。CAR-T细胞相关领域在未来仍将是研究热点。
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