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:Heat up and Destroy: Immunotherapy of "Cold" Tumors Using the Example of Glioblastoma.
Heat up and Destroy: Immunotherapy of "Cold" Tumors Using the Example of Glioblastoma.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
肿瘤被分为“热”或“冷”,取决于癌细胞的内在特性、肿瘤免疫景观的特征、肿瘤微环境(TME)的组成以及潜在的信号机制。这些生物学因素对于界定癌症患者的临床结局和治疗反应至关重要。胶质母细胞瘤的TME是“冷”TME的一个典型例子,其显著阻碍了抗肿瘤免疫。这构成了免疫治疗无效的主要理由。本综述对旨在改变肿瘤免疫特征以实现其有效清除的当代免疫治疗策略进行了全面分析。阐述了免疫检查点抑制剂、过继性细胞治疗和溶瘤病毒(OV)的核心作用机制及未来临床应用。临床前和临床证据的结合表明,基于OV的联合方案可能是“冷”肿瘤的有效治疗策略。
The characterization of tumors as either "hot" or "cold" is determined by intrinsic properties of the cancer cells, the characteristics of the tumor immune landscape, the composition of the tumor microenvironment (TME), and underlying signaling mechanisms. These biological factors are critical in defining the clinical outcomes and therapeutic responses observed in cancer patients. The TME of glioblastoma exemplifies a case of "cold" TME, which significantly hinders antitumor immunity. This constitutes the predominant rationale underlying the ineffectiveness of immunotherapy.
This review provides a thorough analysis of contemporary immunotherapeutic strategies that have been developed for the purpose of altering the immunological characteristics of tumors, with a view to achieving their effective elimination. The core mechanisms of action and future clinical applications of immune checkpoint inhibitors, adoptive cellular therapy, and oncolytic viruses (OV) are delineated. A combination of preclinical and clinical evidence suggests that OV-based combinations could be an effective treatment strategy for "cold" tumors.
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