Deeper phenotyping revealed that loss of CD8+ T cells resulted in depletion of classical monocyte Ly6Chi CX3CR1− or CD86+ subsets in both in WT and IFNγRKO tumours (Fig. 6H), but did not affect F4/80+ macrophage populations (Supplementary Fig. 6D–F). Here, CD86 is linked to neoplasm.