{"title":"基于人工改造 NK 细胞的癌症免疫基因光动力协同疗法。","authors":"Jiale Wu, Kaihong Shi, Wei Chao, Zeyu Qin, Youhui Hu, Yihua Yang, Yuan He, Yabing Hua, Ziming Zhao","doi":"10.2147/IJN.S481368","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>The immunotherapeutic approach utilizing Natural Killer (NK) cells for cancer treatment has garnered significant interest owing to its inherent cytotoxicity, immunomodulatory properties, demonstrated safety in in vivo studies. However, multiple immunosuppressive mechanisms in the tumor microenvironment (TME) suppress the anticancer effect of NK cells in the treatment of solid tumors. Herein, a smart NK cell drug delivery system (DDS) with photo-responsive and TME-responsive properties was designed.</p><p><strong>Methods: </strong>The NK cell DDS consists of two parts: the carrier is living NK cell with pH-low (abbreviated as NK<sub>pH</sub>) insertion peptide on its surface, the cargo is reductive-responsive nanogel (NG) encapsulated siRNA and photosensitizer (abbreviated as SP-NG), the final carrier was abbreviated as SP-NG@ NK<sub>pH</sub>. Firstly, pHLip helped artificially modified NK cell target and anchor onto cancer and exert the efficacy of cellular immunotherapy. Then, the strategy of combining photoactivation and bioreduction responsiveness achieved the precise release of cargos in cancer cells. Finally, the DDS combined the effect of the immunotherapy of NK cell, the gene therapy of siRNA, and the photodynamic therapy of photosensitizer.</p><p><strong>Results: </strong>Under near-infrared laser irradiation, SP-NG@NK<sub>pH</sub> induced an increase in reactive oxygen species (ROS) within cells, exacerbated cell membrane permeability, and allowed for rapid drug release. Within the tumor microenvironment (TME), NG exhibits highly sensitive reducibility for drug release. The SP-NG released from NK cells can be uptaken by tumor cells. When exposed to near-infrared laser irradiation, SP-NG@NK<sub>pH</sub> demonstrates significant tumor-targeting specificity and cytotoxicity.</p><p><strong>Discussion: </strong>The combined effect of the immunotherapy of NK cell, the gene therapy of siRNA, and the photodynamic therapy of photosensitizer obtained a stronger cancer killing effect in vitro and in vivo. Therefore, this versatile NK cell DDS exhibits a good clinical application prospect.</p>","PeriodicalId":14084,"journal":{"name":"International Journal of Nanomedicine","volume":"19 ","pages":"12323-12342"},"PeriodicalIF":6.6000,"publicationDate":"2024-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11587796/pdf/","citationCount":"0","resultStr":"{\"title\":\"Artificially Modified NK Cell-Based Synergistic Immuno-Gene-Photodynamic Therapy for Cancer.\",\"authors\":\"Jiale Wu, Kaihong Shi, Wei Chao, Zeyu Qin, Youhui Hu, Yihua Yang, Yuan He, Yabing Hua, Ziming Zhao\",\"doi\":\"10.2147/IJN.S481368\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>The immunotherapeutic approach utilizing Natural Killer (NK) cells for cancer treatment has garnered significant interest owing to its inherent cytotoxicity, immunomodulatory properties, demonstrated safety in in vivo studies. However, multiple immunosuppressive mechanisms in the tumor microenvironment (TME) suppress the anticancer effect of NK cells in the treatment of solid tumors. Herein, a smart NK cell drug delivery system (DDS) with photo-responsive and TME-responsive properties was designed.</p><p><strong>Methods: </strong>The NK cell DDS consists of two parts: the carrier is living NK cell with pH-low (abbreviated as NK<sub>pH</sub>) insertion peptide on its surface, the cargo is reductive-responsive nanogel (NG) encapsulated siRNA and photosensitizer (abbreviated as SP-NG), the final carrier was abbreviated as SP-NG@ NK<sub>pH</sub>. Firstly, pHLip helped artificially modified NK cell target and anchor onto cancer and exert the efficacy of cellular immunotherapy. Then, the strategy of combining photoactivation and bioreduction responsiveness achieved the precise release of cargos in cancer cells. Finally, the DDS combined the effect of the immunotherapy of NK cell, the gene therapy of siRNA, and the photodynamic therapy of photosensitizer.</p><p><strong>Results: </strong>Under near-infrared laser irradiation, SP-NG@NK<sub>pH</sub> induced an increase in reactive oxygen species (ROS) within cells, exacerbated cell membrane permeability, and allowed for rapid drug release. Within the tumor microenvironment (TME), NG exhibits highly sensitive reducibility for drug release. The SP-NG released from NK cells can be uptaken by tumor cells. When exposed to near-infrared laser irradiation, SP-NG@NK<sub>pH</sub> demonstrates significant tumor-targeting specificity and cytotoxicity.</p><p><strong>Discussion: </strong>The combined effect of the immunotherapy of NK cell, the gene therapy of siRNA, and the photodynamic therapy of photosensitizer obtained a stronger cancer killing effect in vitro and in vivo. 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引用次数: 0
摘要
背景:利用自然杀伤(NK)细胞治疗癌症的免疫疗法因其固有的细胞毒性、免疫调节特性以及在体内研究中表现出的安全性而备受关注。然而,肿瘤微环境(TME)中的多种免疫抑制机制抑制了 NK 细胞治疗实体瘤的抗癌效果。在此,我们设计了一种具有光响应和TME响应特性的智能NK细胞给药系统(DDS):NK细胞药物递送系统由两部分组成:载体是表面含有低pH值插入肽(简称NKpH)的活体NK细胞,货物是包裹siRNA和光敏剂的还原反应纳米凝胶(NG)(简称SP-NG),最终载体简称为SP-NG@ NKpH。首先,pHLip有助于人工改造的NK细胞靶向和锚定癌症,发挥细胞免疫治疗的功效。然后,光激活与生物还原反应相结合的策略实现了载体在癌细胞中的精确释放。最后,DDS 结合了 NK 细胞的免疫疗法、siRNA 的基因疗法和光敏剂的光动力疗法:结果:在近红外激光照射下,SP-NG@NKpH 能诱导细胞内活性氧(ROS)的增加,加剧细胞膜的通透性,使药物快速释放。在肿瘤微环境(TME)中,NG 对药物释放表现出高度敏感的还原性。NK 细胞释放的 SP-NG 可被肿瘤细胞吸收。在近红外激光照射下,SP-NG@NKpH 显示出显著的肿瘤靶向特异性和细胞毒性:NK细胞的免疫治疗、siRNA的基因治疗和光敏剂的光动力治疗相结合,在体外和体内获得了更强的杀癌效果。因此,这种多功能 NK 细胞 DDS 具有良好的临床应用前景。
Artificially Modified NK Cell-Based Synergistic Immuno-Gene-Photodynamic Therapy for Cancer.
Background: The immunotherapeutic approach utilizing Natural Killer (NK) cells for cancer treatment has garnered significant interest owing to its inherent cytotoxicity, immunomodulatory properties, demonstrated safety in in vivo studies. However, multiple immunosuppressive mechanisms in the tumor microenvironment (TME) suppress the anticancer effect of NK cells in the treatment of solid tumors. Herein, a smart NK cell drug delivery system (DDS) with photo-responsive and TME-responsive properties was designed.
Methods: The NK cell DDS consists of two parts: the carrier is living NK cell with pH-low (abbreviated as NKpH) insertion peptide on its surface, the cargo is reductive-responsive nanogel (NG) encapsulated siRNA and photosensitizer (abbreviated as SP-NG), the final carrier was abbreviated as SP-NG@ NKpH. Firstly, pHLip helped artificially modified NK cell target and anchor onto cancer and exert the efficacy of cellular immunotherapy. Then, the strategy of combining photoactivation and bioreduction responsiveness achieved the precise release of cargos in cancer cells. Finally, the DDS combined the effect of the immunotherapy of NK cell, the gene therapy of siRNA, and the photodynamic therapy of photosensitizer.
Results: Under near-infrared laser irradiation, SP-NG@NKpH induced an increase in reactive oxygen species (ROS) within cells, exacerbated cell membrane permeability, and allowed for rapid drug release. Within the tumor microenvironment (TME), NG exhibits highly sensitive reducibility for drug release. The SP-NG released from NK cells can be uptaken by tumor cells. When exposed to near-infrared laser irradiation, SP-NG@NKpH demonstrates significant tumor-targeting specificity and cytotoxicity.
Discussion: The combined effect of the immunotherapy of NK cell, the gene therapy of siRNA, and the photodynamic therapy of photosensitizer obtained a stronger cancer killing effect in vitro and in vivo. Therefore, this versatile NK cell DDS exhibits a good clinical application prospect.
期刊介绍:
The International Journal of Nanomedicine is a globally recognized journal that focuses on the applications of nanotechnology in the biomedical field. It is a peer-reviewed and open-access publication that covers diverse aspects of this rapidly evolving research area.
With its strong emphasis on the clinical potential of nanoparticles in disease diagnostics, prevention, and treatment, the journal aims to showcase cutting-edge research and development in the field.
Starting from now, the International Journal of Nanomedicine will not accept meta-analyses for publication.