推进靶向蛋白降解:pLIRTAC 在胶质瘤与 CAR-T 细胞治疗中的作用
Advancing targeted protein degradation: pLIRTAC's role in glioma and CAR-T cell therapy.
靶向蛋白降解(TPD)的快速发展已显示出对疾病治疗的深远影响。
ALL SOURCES
Advancing targeted protein degradation: pLIRTAC's role in glioma and CAR-T cell therapy.
靶向蛋白降解(TPD)的快速发展已显示出对疾病治疗的深远影响。
Non-Viral Cytokine-Inducible SH2 Containing Protein Locus-Specific Integrated Fibroblast Activation Protein Alpha-Targeting Chimeric Antigen Receptor
CAR-T 细胞已在临床试验中通过靶向 GBM 相关抗原来治疗胶质母细胞瘤(GBM)患者。
Intrathecal CRISPR-edited allogeneic IL-13Rα2 CAR T Cells for recurrent high-grade Glioma: preclinical characterization and phase I trial.
复发高级别胶质母细胞瘤患者的中位生存期为 6-8 个月,治疗选择有限。
From Bench to Bedside: Emerging Paradigms in CAR-T Cell Therapy for Solid Malignancies.
免疫治疗,尤其是CAR-T 细胞疗法,已经彻底改变了血液系统恶性肿瘤和自身免疫性疾病的治疗。
Neuroimmunology-driven CAR T-cell therapeutics for gliomas: translational challenges and clinical trial paradigm innovation.
胶质瘤是一类最具致死性的原发性脑肿瘤,尽管采用最大范围切除、放疗和temozolomide联合的多模式治疗,仍无法治愈。
Preclinical evaluation of antigen-sensitive B7-H3-targeting nanobody-based CAR-T cells in glioblastoma cautions for on-target, off-tumor toxicity.
经体外表征后,B7-H3 nanoCAR-T 细胞在胶质母细胞瘤治疗中显示出前景,但观察到限制性的体内毒性。
Armoring CAR-T Cells Against Exhaustion: Engineering Strategies for Glioblastoma.
胶质母细胞瘤(GBM)是最致命的原发性脑肿瘤,尽管接受强化治疗,中位生存期仍为15个月。
Identification of genetic modifiers enhancing B7-H3-targeting CAR T cell therapy against glioblastoma through large-scale CRISPRi screening.
我们的研究凸显了基于 CRISPR 的基因筛选在探究肿瘤-CAR T 相互作用方面的能力,并鉴定出肿瘤细胞中可成药的潜在靶点,这些靶点赋予肿瘤细胞对 CAR T 细胞杀伤的耐药性。
Chimeric antigen receptor T cell therapy for glioblastoma: overcoming current barriers and strategies to enhance efficacy for therapeutic implications
胶质母细胞瘤(GBM)是一种高度恶性的原发性脑肿瘤,其特点是治疗选择有限且生存结局差。
Chimeric antigen receptor T cell-based targeting of CD317 as a novel immunotherapeutic strategy against glioblastoma.
这些数据揭示了CD317-CAR T细胞疗法在抗胶质母细胞瘤方面具有前景广阔的作用,值得进一步评估,以将这一免疫治疗策略转化为临床神经肿瘤学应用。
MEMBER ACCOUNT
登录成功会直接打开下一页。