Xu Weizhe, Wang Shiyuan, Zhang Jiayi, Wang Fang, Sun Zhaogang, Liu Bei, Ye Jun, Chu Hongqian
Translational Medicine Center, Beijing Chest Hospital, Beijing Tuberculosis and Thoracic Tumor Research Institute, Capital Medical University, Beijing, 101149, China.
State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100050, China.
J Nanobiotechnology. 2025 Jun 2;23(1):410. doi: 10.1186/s12951-025-03464-1.
In recent years, anti-tumor immunity has emerged as a central focus in cancer research, with the rapid advancement of immunotherapy heralding a new era in cancer treatment. Despite the significant potential of immunotherapy, the use of single-agent approaches or limited combination therapies has not consistently yielded optimal therapeutic outcomes. The strategic and controlled integration of diverse immune activation techniques within a single nanoparticle, utilizing a straightforward and universal methodology, continues to present a substantial challenge. Self-assembly, as a simple synthesis method, offers the possibility of combining multiple therapeutic approaches through straightforward means. In this study, we developed a novel approach to construct a biocompatible nanosystem, named Cu-ICG-CpG-FA (CICF), which was synthesized through one-pot coordination-driven self-assembly of Cu ions, CpG oligonucleotides and indocyanine green (ICG), followed by a surface modification with folic acid. Folic acid, as a ligand, can bind to folic acid receptors expressed on the surface of tumor cells. Cu facilitates chemodynamic therapy (CDT) through the Fenton reaction. ICG serves as a therapeutic for photothermal therapy (PTT) and photodynamic therapy (PDT). Moreover, CDT and PTT/PDT can induce immunogenic cell death (ICD), which is further enhanced by the immune-stimulating effect of CpG, thereby improving the tumor immunosuppressive microenvironment. Therefore, CICF provides a simple and efficient approach to synergistic cancer immunotherapy with promising clinical applications.
近年来,抗肿瘤免疫已成为癌症研究的核心焦点,免疫疗法的迅速发展预示着癌症治疗的新时代。尽管免疫疗法具有巨大潜力,但使用单一药物方法或有限的联合疗法并不能始终产生最佳治疗效果。在单个纳米颗粒中利用简单通用的方法对多种免疫激活技术进行战略和可控整合,仍然是一个重大挑战。自组装作为一种简单的合成方法,提供了通过直接手段结合多种治疗方法的可能性。在本研究中,我们开发了一种构建生物相容性纳米系统的新方法,名为Cu-ICG-CpG-FA(CICF),它是通过铜离子、CpG寡核苷酸和吲哚菁绿(ICG)的一锅配位驱动自组装合成的,随后用叶酸进行表面修饰。叶酸作为一种配体,可以与肿瘤细胞表面表达的叶酸受体结合。铜通过芬顿反应促进化学动力疗法(CDT)。ICG用作光热疗法(PTT)和光动力疗法(PDT)的治疗剂。此外,CDT和PTT/PDT可以诱导免疫原性细胞死亡(ICD),而CpG的免疫刺激作用进一步增强了ICD,从而改善肿瘤免疫抑制微环境。因此,CICF为协同癌症免疫治疗提供了一种简单有效的方法,具有广阔的临床应用前景。