PROTAC 工程化蛋白/DNA 纳米抗原是癌症免疫治疗中树突状细胞疫苗的有效增强剂
PROTAC-Engineered Protein/DNA Nanoantigen is a Potent Booster for Dendritic Cell Vaccines in Cancer Immunotherapy.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Magnetic nanoparticles enhance the cellular immune response of dendritic cell tumor vaccines by realizing the cytoplasmic delivery of tumor antigens.
Magnetic nanoparticles enhance the cellular immune response of dendritic cell tumor vaccines by realizing the cytoplasmic delivery of tumor antigens.
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基于树突状细胞(DCs)的肿瘤疫苗具有安全性高、快速激活T细胞等优势,已被批准用于临床肿瘤治疗。然而,传统DC疫苗存在体外DC激活效果差、抗原提呈水平低、细胞活力下降以及体内难以靶向淋巴结等严重问题,导致临床治疗效果不佳。
本研究制备了磁性纳米颗粒Fe 3 O 4 @Ca/MnCO 3,用于主动高效地将抗原递送至DCs胞质,促进抗原交叉提呈和DC激活,最终增强DC疫苗的细胞免疫应答。
结果表明,该磁性纳米颗粒可通过调控磁场主动快速地将抗原递送至DCs胞质,并实现抗原的交叉提呈。同时,纳米颗粒降解产物Mn 2+ 通过干扰素基因刺激蛋白(STING)通路增强免疫刺激,另一降解产物Ca 2+ 则通过增加自噬最终促进细胞免疫应答。利用该磁性纳米颗粒构建的DC疫苗能够更有效地迁移至淋巴结,促进CD8 + T细胞增殖,延长免疫记忆时间,并产生更高水平的抗体。与传统DC疫苗相比,利用该磁性纳米颗粒进行胞质抗原递送为新型DC疫苗的构建提供了新思路。
Dendritic cells (DCs)-based tumor vaccines have the advantages of high safety and rapid activation of T cells, and have been approved for clinical tumor treatment.
However, the conventional DC vaccines have some severe problems, such as poor activation of DCs in vitro, low level of antigen presentation, reduced cell viability, and difficulty in targeting lymph nodes in vivo, resulting in poor clinical therapeutic effects. In this research, magnetic nanoparticles Fe 3 O 4 @Ca/MnCO 3 were prepared and used to actively and efficiently deliver antigens to the cytoplasm of DCs, promote antigen cross-presentation and DC activation, and finally enhance the cellular immune response of DC vaccines. The results show that the magnetic nanoparticles can actively and quickly deliver antigens to the cytoplasm of DCs by regulating the magnetic field, and achieve cross-presentation of antigens.
At the same time, the nanoparticles degradation product Mn 2+ enhanced immune stimulation through the interferon gene stimulating protein (STING) pathway, and another degradation product Ca 2+ ultimately promoted cellular immune response by increasing autophagy.
The DC vaccine constructed with the magnetic nanoparticles can more effectively migrate to the lymph nodes, promote the proliferation of CD8 + T cells, prolong the time of immune memory, and produce higher antibody levels. Compared with traditional DC vaccines, cytoplasmic antigen delivery with the magnetic nanoparticles provides a new idea for the construction of novel DC vaccines.
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