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.
英文原题:γδ T cells as a potential therapeutic agent for glioblastoma.
γδ T cells as a potential therapeutic agent for glioblastoma.
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尽管γδ T细胞仅占T细胞的一小部分,但它们在抵御感染和抑制肿瘤方面发挥着重要作用。凭借其独特的组织定位特性,结合其多种靶标识别机制,γδ T细胞有潜力成为对当前治疗手段无应答的肿瘤的有效解决方案。胶质母细胞瘤(GBM)就是其中一种,它是世界卫生组织分级最高、因此预后最差的恶性脑肿瘤。免疫抑制性肿瘤微环境(TME)和免疫逃逸性胶质瘤干细胞是GBM免疫治疗失败的主要因素。目前,在临床前和临床层面揭示的γδ T细胞强大抗肿瘤功能的鼓舞下,多个研究团队已展示了基于γδ T细胞的GBM治疗的进展。
然而,仍存在若干限制因素阻碍了利用γδ T细胞有效治疗GBM。因此,理解γδ T细胞在抗肿瘤免疫应答中的独特作用以及GBM TME的抑制机制,对于成功的γδ T细胞介导的GBM治疗至关重要。在本综述中,我们总结了γδ T细胞在肿瘤免疫中的效应功能,并讨论了基于γδ T细胞的GBM免疫治疗的当前进展和局限性。
此外,我们提出了未来方向,以克服基于γδ T细胞的GBM免疫治疗的局限性,从而实现GBM的成功治疗。
Although γδ T cells comprise a small population of T cells, they perform important roles in protecting against infection and suppressing tumors. With their distinct tissue-localizing properties, combined with their various target recognition mechanisms, γδ T cells have the potential to become an effective solution for tumors that do not respond to current therapeutic procedures.
One such tumor, glioblastoma (GBM), is a malignant brain tumor with the highest World Health Organization grade and therefore the worst prognosis. The immune-suppressive tumor microenvironment (TME) and immune-evasive glioma stem cells are major factors in GBM immunotherapy failure. Currently, encouraged by the strong anti-tumoral function of γδ T cells revealed at the preclinical and clinical levels, several research groups have shown progression of γδ T cell-based GBM treatment.
However, several limitations still exist that block effective GBM treatment using γδ T cells.
Therefore, understanding the distinct roles of γδ T cells in anti-tumor immune responses and the suppression mechanism of the GBM TME are critical for successful γδ T cell-mediated GBM therapy. In this review, we summarize the effector functions of γδ T cells in tumor immunity and discuss current advances and limitations of γδ T cell-based GBM immunotherapy.
Additionally, we suggest future directions to overcome the limitations of γδ T cell-based GBM immunotherapy to achieve successful treatment of GBM.
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