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:Advancing vaccine-based immunotherapy in glioblastoma treatment.
Advancing vaccine-based immunotherapy in glioblastoma treatment.
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胶质母细胞瘤(GBM)起源于胶质细胞,以侵袭性生长和预后不良为特征。尽管手术切除技术不断进步,完全清除肿瘤仍然具有挑战性,常导致复发并对标准治疗产生耐药。免疫治疗和传统治疗在提高多种癌症的治疗效果方面显示出前景。研究人员持续探索新的治疗方法,尤其是放疗、化疗和手术;然而,胶质母细胞瘤仍然极具挑战性,生存期改善有限。免疫治疗的最新进展,特别是肿瘤疫苗如肽基疫苗和细胞基疫苗(例如树突状细胞疫苗),代表了重大进步,尽管当前临床试验中仍存在局限性。本文综述了基于疫苗的免疫治疗在胶质母细胞瘤治疗中的最新进展。
Glioblastomas (GBMs) originate from glial cells and are characterized by aggressive growth and poor prognosis. Despite advances in surgical resection, complete elimination remains challenging, often leading to recurrence that is resistant to standard therapies. Immunotherapy and conventional treatments show promise in enhancing therapeutic outcomes across various cancers.
Researchers continue to explore new treatments, particularly radiation, chemotherapy, and surgery; however, glioblastoma remains highly challenging, with only modest improvements in survival. Recent progress in immunotherapy, especially with tumor vaccines such as peptide-based and cell-based options (eg, dendritic cell vaccines), represents significant advancements despite the limitations observed in current clinical trials. This article reviews recent developments in vaccine-based immunotherapy for glioblastoma treatment.
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