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    Home > Biochemistry News > Biotechnology News > Scientists reveal the effect of tumor exosomes on NK cells in tumor immunotherapy

    Scientists reveal the effect of tumor exosomes on NK cells in tumor immunotherapy

    • Last Update: 2022-05-01
    • Source: Internet
    • Author: User
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    Tumor-derived exosomes (TDEs) play an important role in multiple aspects of cancer biology, and many studies have clearly shown that TDES can also promote tumor growth by negatively affecting anti-tumor immunity


    Based on this theory, in vitro expansion of NK cells/NK cell lines, such as NK 92 cells, has received extensive attention and research as a promising approach for cancer immunotherapy


    Image credit: https://doi.


    Recently, researchers from the Faculty of Medicine of the Medical University of Isfahan published a review article entitled "Cancer exosomes and natural killer cells dysfunction: biological roles, clinical significance and implications for immunotherapy" in the journal Molecular Cancer, on the role of TDEs in tumor induction.


    Uptake/interaction of TDEs with NK cells

    Uptake/interaction of TDEs with NK cells

    Tumor-derived exosomes (TDEs) can be taken up by various cells through plasma membrane fusion, endocytosis, phagocytosis, micropinocytosis, and lipid raft-mediated internalization, and preferentially by immune cells


    Immune synapses between tumor-derived exosomes and NK cells

    Immune synapses between tumor-derived exosomes and NK cells

    Tumor cells release a large number of immunosuppressive exosomes into the tumor microenvironment and circulation, where they interact with NK cells and deliver their inhibitory contents to NK cells


    Immune synapses between tumor-derived exosomes and NK cells

    Image credit: https://doi.


    Taken together, an in-depth understanding of the pathological roles and mechanisms of TDE-mediated NK cell dysfunction will enable us to further improve the therapeutic potential of NK cells


    references:

    Reza Hosseini et al.


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