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. Author manuscript; available in PMC: 2022 Mar 23.
Published in final edited form as: Cell. 2021 Dec 14;184(26):6262–6280.e26. doi: 10.1016/j.cell.2021.11.031

Figure 6. The immune landscape of colonic tumor subtypes.

Figure 6.

(A) Regulon-based UMAP representation of non-epithelial cells.

(B) Heatmap of marker genes defining each cell type in (A). T - T cell, PLA - Plasma B cell, MYE - Myeloid, MAS - Mast, FIB - Fibroblast cell, END - Endothelial cell, B - B cell.

(C) Scatterplots of cell type representation of (top) polyp and (bottom) CRC subtypes. Points represent individual specimens. Error bars represent SEM of n = 28 for AD, n = 17 for SER, n = 66 for NL, n = 33 for MSS, and n = 34 for MSI-H.

(D and E) Scatterplots of (D) CD4+ T cell and (E) tumor cell-specific signature scores, with each point representing a single cell. Error bars depict SEM of single cells.

(F) MxIF images of CD8+ cells in polyps.

(G) Image quantification of intraepithelial CD8+ cells for n = 20 polyps per type.

(H) MxIF images of CD68+ and MUC5AC+ in cells in polyps.

(I) MxIF scans of intratumoral heterogeneous regions within CRCs (OLFM4+ stem regions versus MUC5AC+ metaplastic regions). MSS CRC only has stem regions. MxIF images of CD8 and CD3 within stem and metaplastic regions. The inset is the quantification of CD8-positive pixels in these regions from MxIF scans of n = 15 MSS and n = 10 MSI-H CRCs.

*p < 0.05, **p < 0.01, ***p < 0.001. See also Figure S6 and Tables S3, S4, and S5.