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:Current Status and Challenges of Oncolytic Virotherapy for the Treatment of Glioblastoma.
Current Status and Challenges of Oncolytic Virotherapy for the Treatment of Glioblastoma.
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尽管经过数十年的研究和大量临床试验,被诊断为胶质母细胞瘤(GBM)的患者预后仍然严峻,中位观察生存期为8个月。GBM是最常见的恶性原发性脑肿瘤,迫切需要新的治疗方法。癌症治疗领域的重大进展,如免疫检查点抑制剂和嵌合抗原受体(CAR)T细胞疗法,尚未改善GBM的结局。手术后继以放化疗联合或不联合肿瘤电场治疗的传统疗法仍是标准治疗。目前正在探索的众多GBM治疗方法之一是病毒疗法。这些疗法通常通过选择性裂解靶肿瘤细胞(称为溶瘤作用)或通过病毒载体靶向递送治疗性转基因来发挥作用。在这篇综述中,我们讨论了其潜在作用机制,并描述了使用这些病毒的近期和当前人体临床试验,重点关注可能最终打破该领域当前停滞范式的有前景的病毒治疗药物。
Despite decades of research and numerous clinical trials, the prognosis of patients diagnosed with glioblastoma (GBM) remains dire with median observed survival at 8 months. There is a critical need for novel treatments for GBM, which is the most common malignant primary brain tumor. Major advances in cancer therapeutics such as immune checkpoint inhibitors and chimeric antigen receptor (CAR) T-cell therapy have not yet led to improved outcomes for GBM. Conventional therapy of surgery followed by chemoradiation with or without tumor treating fields remains the standard of care.
One of the many approaches to GBM therapy currently being explored is viral therapies. These typically work by selectively lysing target neoplastic cells, called oncolysis, or by the targeted delivery of a therapeutic transgene via a viral vector. In this review, we discuss the underlying mechanisms of action and describe both recent and current human clinical trials using these viruses with an emphasis on promising viral therapeutics that may ultimately break the field's current stagnant paradigm.
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