Exosomes as mediators of immune regulation and immunotherapy in cancer

被引:137
|
作者
G. Kugeratski, Fernanda [1 ]
Kalluri, Raghu [1 ,2 ,3 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Metastasis Res Ctr, Dept Canc Biol, Houston, TX 77054 USA
[2] Rice Univ, Dept Bioengn, Houston, TX USA
[3] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
关键词
cancer; exosomes; immunotherapy; lymphoid cells; myeloid cells; CELL-DERIVED EXOSOMES; T-CELLS; DENDRITIC CELLS; ANTITUMOR IMMUNITY; MACROPHAGE POLARIZATION; CLINICAL-SIGNIFICANCE; DELIVERY PLATFORM; TUMOR PROGRESSION; COLORECTAL-CANCER; SUPPRESSOR-CELLS;
D O I
10.1111/febs.15558
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Exosomes are nanosized extracellular vesicles of endosomal origin that enclose a multitude of functional biomolecules. Exosomes have emerged as key players of intercellular communication in physiological and pathological conditions. In cancer, depending on the context, exosomes can oppose or potentiate the development of an aggressive tumor microenvironment, thereby impacting tumor progression and clinical outcome. Increasing evidence has established exosomes as important mediators of immune regulation in cancer, as they deliver a plethora of signals that can either support or restrain immunosuppression of lymphoid and myeloid cell populations in tumors. Here, we review the current knowledge related to exosome-mediated regulation of lymphoid (T lymphocytes, B lymphocytes, and NK cells) and myeloid (macrophages, dendritic cells, monocytes, myeloid-derived suppressor cells, and neutrophils) cell populations in cancer. We also discuss the translational potential of engineered exosomes as immunomodulatory agents for cancer therapy.
引用
收藏
页码:10 / 35
页数:26
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