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工程化巨噬细胞用于黑色素瘤的靶向免疫治疗和药物递送

Engineering macrophages for targeted immunotherapy and drug delivery in melanoma.

作者信息

Liu Xudong, Liu Ye, Zhao Danyu, Shan Dehong, Guo Chenghao, Jia Lianqun

机构信息

College of Integrated Traditional Chinese and Western Medicine, Liaoning University of Traditional Chinese Medicine, Shenyang, Liaoning Province, 116600, China.

Department of Nephrology, Liaoning University of Traditional Chinese Medicine Affiliated Hospital, Shenyang, Liaoning Province, 110000, China.

出版信息

J Transl Med. 2025 Sep 24;23(1):998. doi: 10.1186/s12967-025-06687-w.

Abstract

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.

摘要

黑色素瘤是一种侵袭性很强的皮肤癌,具有很高的转移潜能且预后较差。尽管免疫检查点抑制剂彻底改变了治疗方式,但许多患者仍然没有反应。工程化巨噬细胞已成为免疫治疗和靶向药物递送中有前景的工具。本综述探讨了三种主要策略:通过细胞因子工程增强促炎活性、用嵌合抗原受体(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纳米颗粒介导药物递送平台。临床前证据支持它们调节肿瘤微环境、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,可能克服对当前疗法的耐药性。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。

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