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。
Natural killer cell dysfunction in glioma: from immune evasion to immunotherapy.
自然杀伤(NK)细胞是固有免疫的关键组成部分,无需预先致敏即具有清除肿瘤细胞的能力。
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。
Bispecific antibody-mediated redirection of NKG2D-CAR natural killer cells facilitates dual targeting and enhances antitumor activity.
我们的结果表明,将NKAB抗体与表达激活型NKAR受体的效应细胞联合使用,是一种强大且多用途的策略,可同时增强肿瘤抗原特异性细胞毒性以及NKG2D-CAR和天然NKG2D介导的细胞毒性,这可能特别适用于靶向具有异质性靶抗原表达的肿瘤。
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。
Dual Targeting of Glioblastoma Cells with Bispecific Killer Cell Engagers Directed to EGFR and ErbB2 (HER2) Facilitates Effective Elimination by NKG2D
我们的结果表明,将携带活化NKAR受体的NK细胞与双特异性NKAB抗体联合使用,可实现灵活靶向,从而增强肿瘤抗原特异性细胞毒性并防止免疫逃逸。
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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