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Magnetic Enrichment of Dendritic Cell Vaccine in Lymph Node with Fluorescent-Magnetic Nanoparticles Enhanced Cancer Immunotherapy

机译:磁性磁性纳米粒子增强淋巴结中树突状细胞疫苗的磁富集增强了癌症免疫治疗。

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摘要

Dendritic cell (DC) migration to the lymph node is a key component of DC-based immunotherapy. However, the DC homing rate to the lymphoid tissues is poor, thus hindering the DC-mediated activation of antigen-specific T cells. Here, we developed a system using fluorescent magnetic nanoparticles (α-AP-fmNPs; loaded with antigen peptide, iron oxide nanoparticles, and indocyanine green) in combination with magnetic pull force (MPF) to successfully manipulate DC migration in vitro and in vivo. α-AP-fmNPs endowed DCs with MPF-responsiveness, antigen presentation, and simultaneous optical and magnetic resonance imaging detectability. We showed for the first time that α-AP-fmNP-loaded DCs were sensitive to MPF, and their migration efficiency could be dramatically improved both in vitro and in vivo through MPF treatment. Due to the enhanced migration of DCs, MPF treatment significantly augmented antitumor efficacy of the nanoparticle-loaded DCs. Therefore, we have developed a biocompatible approach with which to improve the homing efficiency of DCs and subsequent anti-tumor efficacy, and track their migration by multi-modality imaging, with great potential applications for DC-based cancer immunotherapy.
机译:树突状细胞(DC)迁移到淋巴结是基于DC的免疫疗法的关键组成部分。然而,淋巴组织的DC归巢率很差,因此阻碍了DC介导的抗原特异性T细胞的活化。在这里,我们开发了一种系统,该系统使用荧光磁性纳米颗粒(α-AP-fmNPs;负载有抗原肽,氧化铁纳米颗粒和吲哚菁绿)与磁性拉力(MPF)相结合,成功地控制了体内和体外的DC迁移。 α-AP-fmNPs使DC具有MPF反应性,抗原呈递以及同时的光学和磁共振成像可检测性。我们首次表明,α-AP-fmNP负载的DC对MPF敏感,通过MPF处理,其迁移效率在体内外均可得到显着提高。由于DC的增强迁移,MPF治疗显着增强了负载纳米颗粒的DC的抗肿瘤功效。因此,我们开发了一种生物相容性方法,可通过其改善DC的归巢效率和随后的抗肿瘤功效,并通过多模态成像跟踪其迁移,在基于DC的癌症免疫治疗中具有巨大的潜在应用。

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