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10.3389/fimmu.2017.00391

http://scihub22266oqcxt.onion/10.3389/fimmu.2017.00391
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C5382194!5382194!28428785
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suck abstract from ncbi


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pmid28428785      Front+Immunol 2017 ; 8 (ä): ä
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  • Interferon Gamma Induces Changes in Natural Killer (NK) Cell Ligand Expression and Alters NK Cell-Mediated Lysis of Pediatric Cancer Cell Lines #MMPMID28428785
  • Aquino-López A; Senyukov VV; Vlasic Z; Kleinerman ES; Lee DA
  • Front Immunol 2017[]; 8 (ä): ä PMID28428785show ga
  • Natural killer (NK) cells have therapeutic potential for cancer due to their capacity for targeting tumor cells without prior sensitization. Our laboratory has developed an NK cell expansion protocol that generates large quantities of NK cells for therapeutic infusion that secret 20 times the amount of interferon gamma (IFN?) than resting NK cells. IFN? can upregulate major histocompatibility complex (MHC)-class I, an inhibitory ligand for NK cells, but can also upregulate intercellular adhesion molecule 1 (ICAM-1) which promotes NK:target cell interaction for an efficient lysis. Due to the opposing effects reported for IFN? on tumor sensitivity to NK cells, we evaluated a panel 22 tumor cell lines from the pediatric preclinical testing program corresponding to different tumor types. We determined the impact of IFN? on their expression of NK cell activating and inhibitory ligands, death receptors, and adhesion molecules using mass cytometry. We also evaluated the effect of IFN? on their sensitivity to NK cell-mediated lysis. Our results show upregulation of PD-L1, ICAM-1, MHC-class I, HLA-DR, CD95/FasR, and CD270/HVEM after IFN? treatment, this upregulation is variable across different tumor types. We also observed a variable impact of IFN? in NK cell-mediated lysis. For six of the cancer cell lines IFN? resulted in increased resistance to NK cells, while for three of them it resulted in increased sensitivity. Modeling of the data suggests that the effect of IFN? on NK cell-mediated tumor lysis is mostly dependent on changes in MHC-class I and ICAM-1 expression. For three of the cell lines with increased resistance, we observed higher upregulation of MHC-class I than ICAM-1. For the cell lines with increased sensitivity after IFN? treatment, we observed upregulation of ICAM-1 exceeding MHC-class I upregulation. ICAM-1 upregulation resulted in increased conjugate formation between the NK cells and tumor cells, which can contribute to the increased sensitivity observed. However, the effects of MHC-class I and ICAM-1 are not readily predictable. Due to the high IFN? secretion of NK cell infusion products, a better understanding of the NK ligands on tumor cells and how they are affected by IFN? is essential to optimize NK cell immunotherapy.
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