FECH:影响 CAR T 细胞表型与功能的新型代谢靶点
FECH, a novel metabolic target influencing CAR T-cell phenotype and function.
这些数据揭示了LIN的双重作用机制,结合了对肿瘤细胞的直接细胞毒性与与血红素生物合成相关的CAR T细胞代谢重编程。
FRONTIER PAPERS
FECH, a novel metabolic target influencing CAR T-cell phenotype and function.
这些数据揭示了LIN的双重作用机制,结合了对肿瘤细胞的直接细胞毒性与与血红素生物合成相关的CAR T细胞代谢重编程。
Perioperative myeloid cell remodeling shapes CAR-T cell efficacy in glioblastoma.
胶质母细胞瘤(GBM)的特征是存在深度免疫抑制的肿瘤微环境(TME),这限制了嵌合抗原受体(CAR)-T 细胞疗法的疗效。
Are the current preclinical models adequate to evaluate CAR-T cell therapy in pediatric high-grade gliomas?
儿童高级别胶质瘤(pHGGs)是侵袭性儿童脑肿瘤,5年生存率低于20%。
Novel CAR T cell blend targeting PDPN and GD2 to overcome glioblastoma heterogeneity.
这种新型 PDPN/GD2 CAR T 细胞混合物在晚期临床前胶质母细胞瘤模型中显示出强效疗效,提示其具有治疗异质性胶质母细胞瘤和解决单抗原 CAR T 细胞疗法相关局限性的潜力。
Engineering next-generation CAR-T cells for glioblastoma treatment: a review of innovations in receptor design, antigen targeting, and therapeutic per
胶质母细胞瘤(GBM)仍是成人中最具侵袭性的原发性恶性脑肿瘤,其特征为预后差、显著的瘤内异质性以及高度免疫抑制的肿瘤微环境(TME)。
Dual targeting of PDPN and GD2 enhances CAR T cell efficacy against glioblastoma and promotes durable tumor control.
Oncofetal antigens as emerging targets in chimeric antigen receptor (CAR)-T cell-based immunotherapies: opportunities and challenges.
肿瘤胚胎抗原因其表达受发育阶段限制且在恶性细胞中频繁重新出现,正成为嵌合抗原受体(CAR)免疫疗法的新兴靶点。
Precision oncology in a dish: patient-derived glioma organoids to guide novel therapeutic strategies.
我们的发现确立 GOs 是胶质瘤治疗筛选中具有临床相关性和生物学真实性的平台。
Recent Locoregional CAR T-Cell Trials for the Treatment of Recurrent Glioblastoma: Implications for Neuro-Oncology Practice.
胶质母细胞瘤仍是成人中最具侵袭性的原发性脑肿瘤之一,尽管采用多模式治疗,生存期也很少超过 15 个月。
De novo H3.3K27M-altered diffuse midline glioma in human brainstem organoids to dissect GD2 CAR T cell function.
弥漫性中线胶质瘤(DMG)是一种高度侵袭性且无法治疗的儿童肿瘤,主要起源于脑桥脑干区域,因此需要开发具有代表性的模型以推动治疗进展。
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