Losing sensitivity to IFNγ may contribute to tumor immune escape, but containment of IFNγ-insensitive tumors is also reported. Here the authors show, by analyzing immune landscape differences between WT and IFNγ receptor-deficient mouse B16-F10 melanoma tumors, that local IFNγ induces complex cellular crosstalk to promote anti-tumor immunity in the latter scenario.
- Vivian W. C. Lau
- Gracie J. Mead
- Audrey Gérard