CD81 通过阻断 CD274/PD-L1 的选择性自噬降解驱动放射抵抗性胶质母细胞瘤的免疫逃逸
CD81 drives immune evasion in radioresistant glioblastoma by blocking selective autophagic degradation of CD274/PD-L1.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Cell-Based Therapy for the Treatment of Glioblastoma: An Update from Preclinical to Clinical Studies.
Cell-Based Therapy for the Treatment of Glioblastoma: An Update from Preclinical to Clinical Studies.
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胶质母细胞瘤(GB)是一种侵袭性中枢神经系统原发肿瘤,约占成人原发性脑肿瘤的60%。其5年生存率极低(约5%),反映出目前标准治疗方案效果有限。这一困境促使研究者不断探索并改进新型疗法。大量临床前研究考察了多种旨在对抗GB、延长生存期的细胞类型,为细胞治疗进入临床试验奠定了基础。本综述旨在总结并讨论截至目前利用干细胞或免疫细胞治疗GB的临床前研究,同时综述近期采用这两类细胞治疗或预防GB患者复发的临床试验。与其他疗法一样,GB细胞治疗仍存在诸多局限。因此,本文还重点介绍若干新技术,例如使用生物材料、支架、纳米颗粒或三维细胞培养体系;这些方法与细胞治疗结合后,可能展现出有前景的发展前景。
Glioblastoma (GB), an aggressive primary tumor of the central nervous system, represents about 60% of all adult primary brain tumors. It is notorious for its extremely low (~5%) 5-year survival rate which signals the unsatisfactory results of the standard protocol for GB therapy. This issue has become, over time, the impetus for the discipline of bringing novel therapeutics to the surface and challenging them so they can be improved.
The cell-based approach in treating GB found its way to clinical trials thanks to a marvelous number of preclinical studies that probed various types of cells aiming to combat GB and increase the survival rate. In this review, we aimed to summarize and discuss the up-to-date preclinical studies that utilized stem cells or immune cells to treat GB.
Likewise, we tried to summarize the most recent clinical trials using both cell categories to treat or prevent recurrence of GB in patients. As with any other therapeutics, cell-based therapy in GB is still hampered by many drawbacks.
Therefore, we highlighted several novel techniques, such as the use of biomaterials, scaffolds, nanoparticles, or cells in the 3D context that may depict a promising future when combined with the cell-based approach.
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