胶质瘤免疫监视与免疫治疗应答交汇处的脑屏障
Brain barriers at the crossroads of glioma immune surveillance and immunotherapy response.
免疫疗法已显著推进癌症治疗;然而,其在胶质瘤中的疗效仍然有限。
FRONTIER PAPERS
Brain barriers at the crossroads of glioma immune surveillance and immunotherapy response.
免疫疗法已显著推进癌症治疗;然而,其在胶质瘤中的疗效仍然有限。
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。
Ferroptosis-armed dendritic cell vaccines for glioma immunotherapy.
这些发现表明,负载铁死亡的DC疫苗能引发强效的肿瘤特异性免疫反应,能够清除小鼠颅内胶质瘤,凸显了其在癌症免疫治疗中的潜力。
Distinct tumor immune microenvironmental landscapes drive divergent immunotherapy responses in glioblastoma.
GBM 包含 3 种功能性 TIME 亚型,其血管-免疫景观存在差异,需要亚型特异性的治疗策略。
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。
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