Fig. 4From: Comparing syngeneic and autochthonous models of breast cancer to identify tumor immune components that correlate with response to immunotherapy in breast cancerMyeloid immune cell subsets differ significantly between the different versions of the MMTV-PyMT breast tumor model. Tumors from the autochthonous MMTV-PyMT model were harvested and single-cell suspensions were generated. Cells (1E6, 1E5, or 1E4) were injected into the mammary fat pad of FVB/NJ wild-type mice. When tumors reached 100 mm3, tumors were obtained and processed into a single-cell suspension for immunophenotyping by flow cytometry. a–d Analysis of cells subsets as a percent of myeloid cells (CD11b+) include a myeloid-derived suppressor cells (MDSC (GR1+)), b PD-L1+F4/80+, c PD-L1– F4/80+, and d other CD11b+ populations; e Analysis of the myeloid cells subsets as a percent of viable cells include f analysis of PD-L1 expression on myeloid cells (CD11b+) and g cancer cells represented by CD45-. h Analysis of the ratio of lymphocytes expressing PD-1. i Analysis of M1-like macrophage markers, CD40+, CD80+, and CD86+ and an M2-like macrophage marker, CD206+, as a ratio of total myeloid cells (CD11b+, top), and mature macrophages (F4/80+, bottom). Graphs show mean ± SEM from at least two independent experiments with at least three mice per group. Each data point represents an individual mouse. Unpaired two-tailed t test. *P<0.05, **P<0.01, ***P<0.001, and ****P<0.001Back to article page