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:A systematic review of immunotherapy in high-grade glioma: learning from the past to shape future perspectives.
A systematic review of immunotherapy in high-grade glioma: learning from the past to shape future perspectives.
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高级别胶质瘤(HGGs)是最常见的恶性原发性脑肿瘤,尽管采用标准的多模式治疗,预后仍然很差。近年来,免疫治疗改变了许多癌症的预后,为HGG治疗带来了更多希望。我们在PubMed、Scopus、Embase和Web of Science数据库进行了全面检索,以纳入相关研究。本研究按照系统评价和荟萃分析首选报告项目(PRISMA)指南进行。最终纳入52篇论文(44项II期和8项III期临床试验),并进一步分为四个不同的亚组:14项肽疫苗试验、15项树突状细胞疫苗(DCV)试验、6项免疫检查点抑制剂(ICI)试验,以及17项包括“主动”和“被动”免疫治疗的杂项组试验。在过去十年中,免疫治疗为提高HGG患者的生存带来了巨大希望;然而,在III期临床试验中,其结果大多令人沮丧。对这些临床结果的深入分析提供了关于导致临床层面失败的常见模式的线索,并有助于塑造神经肿瘤学下一代免疫治疗的前景。
High-grade gliomas (HGGs) constitute the most common malignant primary brain tumor with a poor prognosis despite the standard multimodal therapy. In recent years, immunotherapy has changed the prognosis of many cancers, increasing the hope for HGG therapy.
We conducted a comprehensive search on PubMed, Scopus, Embase, and Web of Science databases to include relevant studies.
This study was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines. Fifty-two papers were finally included (44 phase II and eight phase III clinical trials) and further divided into four different subgroups: 14 peptide vaccine trials, 15 dendritic cell vaccination (DCV) trials, six immune checkpoint inhibitor (ICI) trials, and 17 miscellaneous group trials that included both "active" and "passive" immunotherapies.
In the last decade, immunotherapy created great hope to increase the survival of patients affected by HGGs; however, it has yielded mostly dismal results in the setting of phase III clinical trials. An in-depth analysis of these clinical results provides clues about common patterns that have led to failures at the clinical level and helps shape the perspective for the next generation of immunotherapies in neuro-oncology.
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