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. 2021 Apr 29;184(9):2454–2470.e26. doi: 10.1016/j.cell.2021.03.023

Figure S3.

Figure S3

Immune evasive NPE-IE tumors possess a highly immunosuppressive TME, related to Figure 3

(A) & (B) Gating strategy to define myeloid (A) and lymphoid (B) populations in NPE and NPE-IE tumors.

(C) Representative histograms of PD-L1 expression on microglia and macrophages in NPE-IE tumors (linked to Figure 3E). Control represents fully stained sample minus anti-PD-L1 antibody.

(D) Representative histograms of CD206, CD86 and CD11c expression on macrophages from NPE and NPE-IE tumors. Data derived from 3 tumors randomly down sampled for 50,000 live cells each. Control represents fully stained sample minus either anti-CD206, anti-CD86 or anti-CD11c antibodies.

(E) Flow cytometry quantification of the frequency of macrophages, M-MDSC and microglia positive for expression of PD-L1

(F) Flow cytometry quantification of the frequency of NK cells as a percentage of live cells.

(G) Flow cytometry quantification of the frequency of CD11b+ DCs as a percentage of live cells.

(H) Flow cytometry quantification of CD11b+ DCs positive for expression of PD-L1.

(I) Survival analysis of NSG mice orthotopically injected with NPE-IE cells subjected to IP injection of aCSF-1R or PBS (n = 5 mice + ɑCSF-1R; n = 3 mice +PBS; p = 0.2367).