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:Advancements in dendritic cell vaccination: enhancing efficacy and optimizing combinatorial strategies for the treatment of glioblastoma.
Advancements in dendritic cell vaccination: enhancing efficacy and optimizing combinatorial strategies for the treatment of glioblastoma.
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胶质母细胞瘤(GBM)是高度侵袭性的恶性原发性脑肿瘤。总体预后较差,GBM的管理仍然是一项艰巨的挑战,需要新的治疗策略,如树突状细胞疫苗(DCV)。虽然许多早期临床试验显示可诱导抗肿瘤免疫反应,但结果不一,且取决于试验间各异的众多因素。DCV的优化至关重要;GBM特异性抗原的选择和18F-氟脱氧葡萄糖正电子发射断层扫描(FDG-PET)的应用可能增加重要价值,并最终改善接受胶质母细胞瘤治疗患者的预后。本综述概述了DCV的机制,评估了既往临床试验,并讨论了将DCV整合到胶质母细胞瘤治疗方案中的未来策略。最后,本综述讨论了与DCV使用相关的挑战,并强调了将DCV与标准治疗相结合的潜力。
Glioblastomas (GBM) are highly invasive, malignant primary brain tumors. The overall prognosis is poor, and management of GBMs remains a formidable challenge, necessitating novel therapeutic strategies such as dendritic cell vaccinations (DCVs). While many early clinical trials demonstrate an induction of an antitumoral immune response, outcomes are mixed and dependent on numerous factors that vary between trials.
Optimization of DCVs is essential; the selection of GBM-specific antigens and the utilization of 18 F-fludeoxyglucose Positron Emission Tomography (FDG-PET) may add significant value and ultimately improve outcomes for patients undergoing treatment for glioblastoma.
This review provides an overview of the mechanism of DCV, assesses previous clinical trials, and discusses future strategies for the integration of DCV into glioblastoma treatment protocols. To conclude, the review discusses challenges associated with the use of DCVs and highlights the potential of integrating DCV with standard therapies.
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