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 therapies for glioblastoma: Promising tools against tumor heterogeneity.
Cell-based therapies for glioblastoma: Promising tools against tumor heterogeneity.
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胶质母细胞瘤(GBM)是一种高度侵袭性的肿瘤,对生活质量造成毁灭性影响,生存率极低。患者的有效治疗选择非常有限。尽管我们在对其分子、免疫和微环境景观的理解方面取得了重大进展,但在各种实体瘤中观察到的靶向小分子药物和免疫检查点抑制剂的成功并未转化为GBM的疗效。然而,这些发现揭示了GBM令人难以置信的异质性及其在治疗失败和生存中的作用。新型细胞治疗技术正在肿瘤学领域取得成功,并具有使其特别适合克服GBM所带来挑战的特性,例如对肿瘤异质性的更强抵抗力、模块化、局部递送和安全性。考虑到这些优势,我们编写了这篇关于GBM细胞治疗的综述文章,重点关注细胞免疫疗法和基于干细胞的疗法,以评估其效用。我们根据其特异性对其进行分类,回顾其临床前和临床数据,并提取有价值的见解以帮助指导未来的细胞治疗开发。
Glioblastoma (GBM) is a highly aggressive tumor with a devastating impact on quality-of-life and abysmal survivorship. Patients have very limited effective treatment options. The successes of targeted small molecule drugs and immune checkpoint inhibitors seen in various solid tumors have not translated to GBM, despite significant advances in our understanding of its molecular, immune, and microenvironment landscapes. These discoveries, however, have unveiled GBM's incredible heterogeneity and its role in treatment failure and survival.
Novel cellular therapy technologies are finding successes in oncology and harbor characteristics that make them uniquely suited to overcome challenges posed by GBM, such as increased resistance to tumor heterogeneity, modularity, localized delivery, and safety. Considering these advantages, we compiled this review article on cellular therapies for GBM, focusing on cellular immunotherapies and stem cell-based therapies, to evaluate their utility.
We categorize them based on their specificity, review their preclinical and clinical data, and extract valuable insights to help guide future cellular therapy development.
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