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:Emerging macrophage-based therapies for cancer: a review of preclinical and clinical advances.
Emerging macrophage-based therapies for cancer: a review of preclinical and clinical advances.
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巨噬细胞是许多实体瘤中数量最多的免疫细胞,如今已不再仅被视为癌症的帮凶,也被视为强有力的治疗盟友。本综述梳理了巨噬细胞免疫疗法的快速发展,包括CD47/SIRPα检查点阻断、CAR巨噬细胞以及巨噬细胞-药物偶联物(MDC)。文章重点介绍正在兴起的前沿方向——基于RNA的重编程、表观遗传调节、小激活RNA和环状RNA策略,以及巨噬细胞来源的细胞外囊泡;这些方向正在重新定义如何靶向或利用肿瘤相关巨噬细胞。与早期TAM综述不同,本文整合了进行中和已完成临床试验的结果,介绍经典清除和极化方法之外的治疗平台,并将巨噬细胞既视为靶细胞,也视为递送载体。通过聚焦创新策略及其临床转化挑战,本文旨在为推动下一代癌症免疫治疗的研究人员和临床医生提供前瞻性指南。
Macrophages, the most abundant immune cells in many solid tumors, are no longer viewed solely as accomplices of cancer but as powerful therapeutic allies. This review charts the rapid rise of macrophage-based immunotherapies, from CD47/SIRPα checkpoint blockade and CAR-macrophages to macrophage-drug conjugates (MDCs).
We emphasize emerging frontiers - RNA-based reprogramming, epigenetic modulation, small activating RNA and circRNA approaches, and macrophage-derived extracellular vesicles - that are redefining how tumor-associated macrophages can be targeted or harnessed.
Distinct from earlier TAM reviews, we integrate outcomes from ongoing and completed clinical trials, highlight therapeutic platforms beyond classical depletion and polarization, and frame macrophages not only as targets but also as delivery vehicles. By spotlighting both innovative strategies and the challenges of moving them into the clinic, we aim to provide a forward-looking guide for researchers and clinicians shaping the next generation of cancer immunotherapy.
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 →
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