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:γδ T Cells in Glioblastoma Multiforme: Novel Roles and Therapeutic Opportunities.
γδ T Cells in Glioblastoma Multiforme: Novel Roles and Therapeutic Opportunities.
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多形性胶质母细胞瘤(GBM)是最具侵袭性的癌症之一,由于其高度免疫抑制的微环境和对常规疗法的耐药性,治疗选择有限。γδ T 细胞以其强大的抗肿瘤活性和不依赖 HLA 分子识别肿瘤抗原的能力而闻名,已成为一种有前景的治疗策略。本综述探讨了 γδ T 细胞在胶质母细胞瘤中的作用,重点关注其功能可塑性、细胞毒性机制以及与肿瘤微环境各组分的相互作用。我们审视了影响 γδ T 细胞向促肿瘤或抗肿瘤表型极化的因素,并分析了支持其在 GBM 治疗中应用的临床前研究结果。此外,我们讨论了潜在的联合方案——包括免疫检查点抑制剂、细胞因子刺激和过继性细胞转移技术——以增强 γδ T 细胞的治疗效果和持久性。理解 GBM 与 γδ T 细胞之间的动态关系,可能为旨在克服免疫逃逸和改善临床结局的创新免疫治疗策略铺平道路。
Glioblastoma multiforme (GBM) is one of the most aggressive cancers, with limited treatment options due to its highly immunosuppressive microenvironment and resistance to conventional therapies. γδ T cells, known for their potent antitumor activity and ability to recognize tumor antigens independently of HLA molecules, have emerged as a promising therapeutic strategy. This review explores the role of γδ T cells in glioblastoma, focusing on their functional plasticity, cytotoxic mechanisms, and interactions with components of the tumor microenvironment.
We examine the factors that influence γδ T cell polarization toward pro- or anti-tumor phenotypes and analyze preclinical findings that support their application in GBM treatment.
Furthermore, we discuss potential combinatory approaches-including immune checkpoint inhibitors, cytokine stimulation, and adoptive cell transfer techniques-to enhance the therapeutic effectiveness and persistence of γδ T cells. Understanding the dynamics between GBM and γδ T cells may pave the way for innovative immunotherapeutic strategies aimed at overcoming immune evasion and improving clinical outcomes.
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