RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Neoantigen-specific mRNA/DC vaccines for effective anticancer immunotherapy.
Neoantigen-specific mRNA/DC vaccines for effective anticancer immunotherapy.
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基于新抗原的个体化抗癌疫苗的开发代表了肿瘤免疫治疗的新方向。树突状细胞(DC)肿瘤疫苗构建的最新进展涉及将编码新抗原的 mRNA 负载到 DC 中,这允许快速生产并适合个体化制备。细胞穿透肽(CPP)正在成为生物递送系统,其中带负电荷的核酸可以缠绕到阳离子 CPP 骨架上以形成纳米级复合物。这种制备方法有利于标准化。如果 DC 能够高水平表达和呈递新抗原 mRNA,则具有广阔的应用潜力。在本研究中,我们使用来自小鼠结肠癌(MC38)的候选新抗原开发了新抗原-mRNA/DC 疫苗,并检查了其免疫和抗肿瘤效果。结果表明,新抗原-mRNA/DC 疫苗诱导了强烈的 T 细胞免疫反应,并表现出显著的抗肿瘤效果,有效防止肿瘤生长。我们的研究为进一步优化 DC 疫苗的制备和降低其成本提供了实验基础。
The development of personalized anticancer vaccines based on neoantigens represents a new direction in cancer immunotherapy. The latest advancement in dendritic cell (DC) tumor vaccine construction involves loading DC with mRNA-encoding neoantigens, which allows for rapid production and is suitable for personalized preparation. Cell-penetrating peptides (CPPs) are emerging as biological delivery systems in which negatively charged nucleic acids can be wound onto the cationic CPP backbone to form nanoscale complexes.
This preparation method facilitates standardization. If DC can express and present neoantigen mRNA at high levels, it holds promising application potential. In this study, we developed a neoantigen-mRNA/DC vaccine using candidate neoantigens from mouse colon cancer (MC38) and examined its immune and antitumor effects. The results demonstrated that neoantigen-mRNA/DC vaccines induced strong T cell immune responses and exhibited significant antitumor effects, effectively preventing tumor growth.
Our study provides an experimental basis for further optimizing the preparation of DC vaccines and reducing their costs.
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