Tumor-derived extracellular vesicles modulate innate immune responses to affect tumor progression

被引:23
作者
Wang, Siqi [1 ,2 ]
Sun, Jiaxin [1 ,2 ]
Dastgheyb, Raha M. M. [3 ]
Li, Zhigang [1 ]
机构
[1] Sun Yat sen Univ, Affiliated Hosp 7, Sci Res Ctr, Shenzhen, Peoples R China
[2] Sun Yat sen Univ, Sch Med, Shenzhen, Peoples R China
[3] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
关键词
macrophages; dendritic cells; neutrophils; natural killer cells; tumor-derived extracellular vesicles (TDEVs); tumor progression; NATURAL-KILLER-CELLS; M2 MACROPHAGE POLARIZATION; NF-KAPPA-B; CANCER-CELLS; DENDRITIC CELLS; ACTIVATED MACROPHAGES; EXOSOMES; PROMOTE; MICROVESICLES; EXPRESSION;
D O I
10.3389/fimmu.2022.1045624
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immune cells are capable of influencing tumor progression in the tumor microenvironment (TME). Meanwhile, one mechanism by which tumor modulate immune cells function is through extracellular vesicles (EVs), which are cell-derived extracellular membrane vesicles. EVs can act as mediators of intercellular communication and can deliver nucleic acids, proteins, lipids, and other signaling molecules between cells. In recent years, studies have found that EVs play a crucial role in the communication between tumor cells and immune cells. Innate immunity is the first-line response of the immune system against tumor progression. Therefore, tumor cell-derived EVs (TDEVs) which modulate the functional change of innate immune cells serve important functions in the context of tumor progression. Emerging evidence has shown that TDEVs dually enhance or suppress innate immunity through various pathways. This review aims to summarize the influence of TDEVs on macrophages, dendritic cells, neutrophils, and natural killer cells. We also summarize their further effects on the progression of tumors, which may provide new ideas for developing novel tumor therapies targeting EVs.
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页数:18
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