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:Immunotherapeutic Strategies for the Treatment of Glioblastoma: Current Challenges and Future Perspectives.
Immunotherapeutic Strategies for the Treatment of Glioblastoma: Current Challenges and Future Perspectives.
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尽管历经数十年研究并采用当前最佳治疗,4级胶质母细胞瘤(GBM)仍几乎无一例外致死,患者中位总生存期不足2年。免疫治疗近期进展重新点燃了利用免疫学方法抗癌的兴趣。然而,当前免疫疗法迄今未达到预期,在GBM治疗从实验室走向临床的过程中仅取得有限成果。了解GBM的内在特征对于开发有效抗肿瘤策略、改善患者预期寿命和生活状况至关重要。本文全面综述显著影响当前常规疗法和免疫疗法的GBM独特特征,并介绍目前正在临床评估的GBM免疫治疗策略,特别关注进入III期临床研究的疗法,包括免疫检查点抑制剂、过继性T细胞疗法、疫苗策略(如RNA、DNA和肽疫苗)及病毒疗法。最后探讨GBM免疫治疗领域的新型创新策略和未来前景。
Despite decades of research and the best up-to-date treatments, grade 4 Glioblastoma (GBM) remains uniformly fatal with a patient median overall survival of less than 2 years. Recent advances in immunotherapy have reignited interest in utilizing immunological approaches to fight cancer.
However, current immunotherapies have so far not met the anticipated expectations, achieving modest results in their journey from bench to bedside for the treatment of GBM. Understanding the intrinsic features of GBM is of crucial importance for the development of effective antitumoral strategies to improve patient life expectancy and conditions. In this review, we provide a comprehensive overview of the distinctive characteristics of GBM that significantly influence current conventional therapies and immune-based approaches.
Moreover, we present an overview of the immunotherapeutic strategies currently undergoing clinical evaluation for GBM treatment, with a specific emphasis on those advancing to phase 3 clinical studies. These encompass immune checkpoint inhibitors, adoptive T cell therapies, vaccination strategies (i. e. , RNA-, DNA-, and peptide-based vaccines), and virus-based approaches.
Finally, we explore novel innovative strategies and future prospects in the field of immunotherapy for GBM.
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