Fusion of Dendritic Cells and Cancer-Associated Fibroblasts for Activation of Anti-Tumor Cytotoxic T Lymphocytes

细胞毒性T细胞 间质细胞 抗原提呈细胞 白细胞介素12 CD40 肿瘤微环境 分子生物学 流式细胞术 骨髓 癌症研究 免疫系统 体外 细胞生物学 化学 生物 免疫学 生物化学
作者
Liwen Qian,Zhuoran Tang,Shihua Yin,Fengzhen Mo,Xiaomei Yang,Xiaoqiong Hou,Aiqun Liu,Xiaoling Lü
出处
期刊:Journal of Biomedical Nanotechnology [American Scientific Publishers]
卷期号:14 (10): 1826-1835 被引量:39
标识
DOI:10.1166/jbn.2018.2616
摘要

Here we explored the fusion of dendritic cells (DCs), potent antigen-presenting cells that initiate primary immune responses, with cancer-associated fibroblasts (CAFs), which are a stromal component needed for tumor progression, with the aim of stimulating T cells to inhibit tumor growth. Dendritic cells from the bone marrow of BALB/c mice were co-cultured with CAFs from H22 mouse hepatoma cells. CAFs were found to express fibroblast activation protein and α-smooth muscle actin by flow cytometry, Western blotting and immunofluorescence. Polyethylene glycol was added to the co-culture medium to encourage fusion, and the ability of the resulting fusion cells to produce TNF-α, IL-1β, IL-6, and IL-12p70 was confirmed using ELISA. These fusion cells efficiently stimulated T lymphocytes in vitro, causing them to generate IFN-α and IFN-γ. T cells activated by DC/CAF fusion cells led to strong CTL response against CAFs in vitro. The activated T cells also inhibited growth of H22 xenografts in vivo. These results indicate that DC/CAF fusion cells show potential for stimulating T cells as a novel anti-tumor vaccine.

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