免疫检查点阻断通过扩增效应 CD8⁺ T 细胞克隆增强淋巴细胞清除性化疗诱导的抗肿瘤免疫
Immune Checkpoint Blockade Augments Lymphodepleting Chemotherapy-Induced Antitumor Immunity by Expanding Effector CD8+ T-cell Clones.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Engineering macrophages for targeted immunotherapy and drug delivery in melanoma.
Engineering macrophages for targeted immunotherapy and drug delivery in melanoma.
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黑色素瘤是一种高度侵袭性的皮肤癌,具有高转移潜能和不良预后。尽管免疫检查点抑制剂已经彻底改变了治疗格局,但许多患者仍然无应答。工程化巨噬细胞已成为免疫治疗和靶向药物递送中颇具前景的工具。本综述探讨了三大策略:通过细胞因子工程增强促炎活性、嵌合抗原受体(CAR)修饰巨噬细胞以实现抗原特异性靶向,以及基于巨噬细胞的平台用于纳米颗粒介导的药物递送。临床前证据支持其调节肿瘤微环境、增强 T 细胞募集和减少肿瘤生长的能力。这些策略提供了互补的方法,可能克服对当前治疗的耐药性。我们还讨论了当前的局限性和未来方向,强调了这些基于巨噬细胞的干预措施临床转化的潜力。
Melanoma is a highly aggressive skin cancer with a high metastatic potential and poor prognosis. While immune checkpoint inhibitors have revolutionized treatment, many patients remain unresponsive. Engineered macrophages have emerged as promising tools in immunotherapy and targeted drug delivery.
This review explores three major strategies: cytokine engineering to enhance pro-inflammatory activity, chimeric antigen receptor (CAR)-modified macrophages for antigen-specific targeting, and macrophage-based platforms for nanoparticle-mediated drug delivery. Preclinical evidence supports their capacity to modulate the tumor microenvironment, enhance T cell recruitment, and reduce tumor growth. These strategies offer complementary approaches that may overcome resistance to current therapies.
We also discuss current limitations and future directions, emphasizing the potential for clinical translation of these macrophage-based interventions.
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