胶质母细胞瘤的代谢与翻译后脆弱性:二硫死亡、糖基化及对 CAR-T 治疗的启示
Metabolic and Post-Translational Vulnerabilities of Glioblastoma: Disulfidptosis, Glycosylation, and Implications for CAR-T Therapy.
胶质母细胞瘤(GB)仍是治疗抵抗性最强的实体瘤之一,其特征是显著的代谢可塑性、瘤内异质性和高度免疫抑制的微环境。
ALL SOURCES
Metabolic and Post-Translational Vulnerabilities of Glioblastoma: Disulfidptosis, Glycosylation, and Implications for CAR-T Therapy.
胶质母细胞瘤(GB)仍是治疗抵抗性最强的实体瘤之一,其特征是显著的代谢可塑性、瘤内异质性和高度免疫抑制的微环境。
Locoregional infusion of EGFR806-CAR T cells for recurrent or refractory pediatric CNS tumors: Results of the completed BrainChild02 phase 1 clinical
颅内输注EGFR806-CAR T细胞在测试剂量下可耐受,最佳反应为疾病稳定。EGFR是针对儿童脑肿瘤,特别是高级别胶质瘤的细胞治疗的潜在有用靶点。
Enable CAR T cell immunotherapy in glioblastoma by modifying its microenvironment via oncolytic adenovirus encoding bispecific T cell engager.
我们的多模式 OV-BiTE 联合 CAR T 细胞免疫治疗能够克服免疫抑制性肿瘤微环境和 GBM 对治疗的耐药。
Anti-VEGF therapy improves EGFR-vIII-CAR-T cell delivery and efficacy in syngeneic glioblastoma models in mice.
事实上,美国 FDA(食品药品监督管理局)在过去 3 年里已批准了 7 种不同的抗 VEGF 药物与免疫检查点阻断剂的联合方案,用于肝癌、肾癌、肺癌和子宫内膜癌。
Increased EGFRvIII Epitope Accessibility after Tyrosine Kinase Inhibitor Treatment of Glioblastoma Cells Creates More Opportunities for Immunotherapy.
我们的结果表明,EGFRvIII 特异性 L8A4 抗体既可识别 EGFRvIII 单体,也可识别共价二聚体,与半胱氨酸桥接结构无关。
Programmable Attenuation of Antigenic Sensitivity for a Nanobody-Based EGFR Chimeric Antigen Receptor Through Hinge Domain Truncation.
这些结果表明,铰链长度调节提供了一种可编程策略,用于调节靶向膜近端表位的 CARs 的抗原敏感性,并可用于 CAR 优化和提高肿瘤选择性。
CAR T Cell Therapy in Primary Brain Tumors: Current Investigations and the Future.
CAR-T 细胞(CAR T细胞)是经过工程化改造的细胞,表达针对特定肿瘤抗原(TA)的嵌合抗原受体(CAR),从而能够识别并清除癌细胞。
Comparative evaluation of CAR-expressing T-, NK-, NKT-cells, and macrophages in an immunocompetent mouse glioma model.
这些数据为在免疫功能健全的胶质瘤环境中哪些免疫细胞能介导有效的抗胶质瘤应答提供了有价值的依据。
Clinical progress in the development of CAR T cells to treat malignant glioma.
在研 CAR-T 细胞疗法的快速演进预示着胶质瘤治疗未来的巨大潜力。
EGFRVIII and EGFR targeted chimeric antigen receptor T cell therapy in glioblastoma.
胶质母细胞瘤是最常见的原发性脑肿瘤。
MEMBER ACCOUNT
登录成功会直接打开下一页。