48 49 Intriguingly, we indeed saw that treatment of THP1-reporter cells with high concentrations of TGF-β (like concentrations recovered from OV-patients in UZL-CSI cohort) induced highly significant IFN/ISG (but not NFkB) responses ( figure 3H, I ), thereby suggesting a context-dependent pro-immunogenic role for TGF-β.
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Peripherally-driven myeloid NFkB and IFN/ISG responses predict malignancy risk, survival, and immunotherapy regime in ovarian cancer.
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