免疫系统
细胞外小泡
细胞外
细胞生物学
生物
免疫学
癌症研究
化学
生物化学
作者
Wen Liu,Yuki Takahashi,Masaki Morishita,Makiya Nishikawa,Yoshinobu Takakura
出处
期刊:Nanomedicine
[Future Medicine]
日期:2020-07-01
卷期号:15 (17): 1641-1652
被引量:10
标识
DOI:10.2217/nnm-2020-0071
摘要
Aim: Tumor-derived small extracellular vesicles (TEVs) are considered for use in inducing tumor antigen-specific immune responses as they contain tumor antigens. The delivery of tumor antigens to the antigen presentation cells (especially dendritic cells [DCs]), and the activation of DCs are the main challenges of TEV therapy. Materials & methods: TEVs were modified with CD40 ligand (CD40L), which can target CD40 expressed on the surface of DCs and can activate them via CD40L-CD40 interactions. Results: It was found that CD40L-TEVs were efficiently taken up by DCs and also activated them. Moreover, tumor antigens were efficiently presented to the T cells by DCs treated with CD40L-TEVs. Conclusion: This study proved that CD40L-modification of TEVs will be helpful for further development of TEV-based tumor vaccination.
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