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:Recent Development in NKT-Based Immunotherapy of Glioblastoma: From Bench to Bedside.
Recent Development in NKT-Based Immunotherapy of Glioblastoma: From Bench to Bedside.
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多形性胶质母细胞瘤(GBM)是一种侵袭性强且预后极差的疾病,中位总生存期约为15个月,5年生存率为7.2%。由于基因突变、耐药性、血脑屏障(BBB)/血脑肿瘤屏障(BBTB)的破坏以及免疫抑制环境的复杂性,GBM的治疗方法仍面临重大挑战。传统疗法,包括手术、放疗和替莫唑胺标准化疗,并未使GBM患者的总生存期获得令人满意的改善。在癌症免疫治疗方法中,我们提出,采用恒定自然杀伤T(iNKT)细胞和细胞因子诱导的杀伤(CIK)细胞的辅助NKT免疫治疗可能改善这一毁灭性疾病的临床状况。鉴于此,本文主要基于体外/体内实验、临床试验以及具有未来治疗潜力的联合方案,讨论当前针对GBM的NKT治疗策略。
Glioblastoma multiforme (GBM) is an aggressive and dismal disease with a median overall survival of around 15 months and a 5-year survival rate of 7. 2%. Owing to genetic mutations, drug resistance, disruption to the blood-brain barrier (BBB)/blood-brain tumor barrier (BBTB), and the complexity of the immunosuppressive environment, the therapeutic approaches to GBM represent still major challenges. Conventional therapies, including surgery, radiotherapy, and standard chemotherapy with temozolomide, have not resulted in satisfactory improvements in the overall survival of GBM patients.
Among cancer immunotherapeutic approaches, we propose that adjuvant NKT immunotherapy with invariant NKT (iNKT) and cytokine-induced killer (CIK) cells may improve the clinical scenario of this devastating disease. Considering this, herein, we discuss the current strategies of NKT therapy for GBM based primarily on in vitro/in vivo experiments, clinical trials, and the combinatorial approaches with future therapeutic potential.
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