RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Current strategies and novel immunotherapeutic approaches for overcoming immune resistance in glioblastoma.
Current strategies and novel immunotherapeutic approaches for overcoming immune resistance in glioblastoma.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
胶质母细胞瘤(GBM)是侵袭性最强的原发性恶性脑肿瘤,具有增殖迅速、广泛浸润和遗传异质性显著等特点。尽管已有手术切除、放疗和化疗等标准治疗,GBM患者预后仍然较差,中位生存期约为15个月。免疫治疗近期进展带来了创新方法,旨在利用免疫系统特异性靶向并清除GBM细胞。这些策略包括细胞因子治疗、免疫检查点抑制剂、嵌合抗原受体(CAR)T细胞和自然杀伤(NK)细胞疗法、RNA免疫疗法以及纳米颗粒介导的药物递送系统。此外,CRISPR/Cas9基因编辑、外泌体递送、STING通路激活及人工智能指导的个体化治疗等新兴技术,有望克服免疫抑制性肿瘤微环境并提高治疗效果。本综述全面介绍这些前沿方法,讨论其作用机制、临床潜力、现有局限及未来方向,以促进开发更有效的GBM免疫疗法。
Glioblastoma (GBM) is the most aggressive primary malignant brain tumor, characterized by rapid proliferation, extensive invasion, and significant genetic heterogeneity. Despite the availability of standard treatments such as surgical resection, radiotherapy, and chemotherapy, the prognosis for GBM patients remains poor, with a median survival of approximately 15 months.
Recent advances in immunotherapy have introduced innovative approaches aimed at leveraging the immune system to specifically target and eliminate GBM cells. These strategies include cytokine-based therapies, immune checkpoint inhibitors, chimeric antigen receptor (CAR) T-cell and natural killer (NK) cell therapies, RNA-based immunotherapies, and nanoparticle-mediated drug delivery systems.
Furthermore, emerging technologies such as CRISPR/Cas9 gene editing, exosome-based delivery, STING pathway activation, and AI-guided personalized treatment have shown promise in overcoming the immunosuppressive tumor microenvironment and enhancing therapeutic efficacy. This review provides a comprehensive overview of these cutting-edge approaches, discussing their mechanisms, clinical potential, current limitations, and future directions for the development of more effective immunotherapies for GBM.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。