Department of Surgical Oncology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Cancer Institute (Key Laboratory of Cancer Prevention & Intervention, National Ministry of Education, Provincial Key Laboratory of Molecular Biology in Medical Sciences), Zhejiang University School of Medicine, Hangzhou, China.
J Immunol Res. 2017;2017:1073947. doi: 10.1155/2017/1073947. Epub 2017 May 31.
Exosomes are a kind of cell-released membrane-form structures which contain proteins, lipids, and nucleic acids. These vesicular organelles play a key role in intercellular communication. Numerous experiments demonstrated that tumor-related exosomes (TEXs) can induce immune surveillance in the microenvironment in vivo and in vitro. They can interfere with the maturation of DC cells, impair NK cell activation, induce myeloid-derived suppressor cells, and educate macrophages into protumor phenotype. They can also selectively induce effector T cell apoptosis via Fas/FasL interaction and enhance regulatory T cell proliferation and function by releasing TGF-. In this review, we focus on the TEX-induced immunosuppression and microenvironment change. Based on the truth that TEXs play crucial roles in suppressing the immune system, studies on modification of exosomes as immunotherapy strategies will also be discussed.
外泌体是一种细胞释放的膜状结构,包含蛋白质、脂质和核酸。这些囊泡细胞器在细胞间通讯中发挥着关键作用。大量实验表明,肿瘤相关的外泌体(TEXs)可以在体内和体外诱导微环境中的免疫监视。它们可以干扰 DC 细胞的成熟,损害 NK 细胞的激活,诱导髓源抑制细胞,并将巨噬细胞诱导为促肿瘤表型。它们还可以通过 Fas/FasL 相互作用选择性地诱导效应 T 细胞凋亡,并通过释放 TGF-来增强调节性 T 细胞的增殖和功能。在这篇综述中,我们重点关注 TEX 诱导的免疫抑制和微环境变化。基于 TEX 在抑制免疫系统中发挥关键作用的事实,我们还将讨论对外泌体进行修饰作为免疫治疗策略的研究。