Tumor-Derived Exosome and Immune Modulation

نویسندگان

چکیده

Tumor cells, like most other release exosomes called tumor-derived (TEX) and are vital for intercellular communication. TEX membrane-bound extracellular vesicles (EVs), containing unique cargo reminiscent of the parent tumor cells possess immunomodulatory functions. carries factors that directly promote immunosuppression in microenvironment indirectly attract immunosuppressive T-regulatory (Treg) cells. The tumor-secreted can transfer their by multiple mechanisms fusion, phagocytosis, receptor-mediated endocytosis, activating recipient engages releases cytokines, inactivating natural killer (NK) T-cells apoptosis. Tumor-derived also soluble to suppress dendritic cell (DC) maturation while expansion immune-suppressive Myeloid-derived suppressor (MDSCs) Regulatory T Several studies have shown relevance tumor-associated antigens (TAA) reducing efficacy cancer immunotherapy adoptive therapy. Hence understanding basic biology mechanism TEX-mediated is critical discovering biomarkers finding better therapy approaches. In this chapter, we discussed biogenesis, TEX’s structural molecular features, immunosuppression, its relation immunotherapy.

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ژورنال

عنوان ژورنال: Physiology

سال: 2022

ISSN: ['1548-9221', '1548-9213']

DOI: https://doi.org/10.5772/intechopen.103718