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. 2023 Apr 17;31(7):2105–2119. doi: 10.1016/j.ymthe.2023.04.008

Figure 1.

Figure 1

HFRT induces significant alterations of MDSCs and T cells within tumors

(A) Treatment scheme. (B) Bar plots showing fractions of CD45+ tumor-infiltrating immune cells (TIICs), CD11c+ DCs, CD49b+ NK cells, CD11b+ F4/80+ macrophages, or CD4+ CD25+ Foxp3+ Treg cells in CT26 tumors. (C and E) Representative flow plots of CD45+ TIICs, CD3+, CD4+, CD8+ T cells, Gr-1+ CD11b+ MDSCs, Gr-1+ CD11b+ Ly6Ghigh polymorphonuclear (PMN)-MDSCs, or Gr-1+ CD11b+ Ly6Glow M-MDSCs in CT26 tumors (percentage of all live cells) in tumor. (D and F) Bar plots showing fractions of total MDSCs, PMN-MDSCs, M-MDSCs, CD3+, CD4+, or CD8+ T cells (percentage of all live cells) in CT26 tumor. (G) Representative multicolor immunofluorescence images of tumor specimens from rectal cancer patients who received 5 × 5 Gy preoperative HFRT (n = 3; scale bar: 100 μm; magnification 20×; MDSCs: red arrowheads, T cells: white arrowheads). (H–K) Bar plots showing fractions of CD45+ TIICs, CD3+, CD4+, CD8+ T cells, MDSCs, PMN-MDSCs, and M-MDSCs (percentage of all live cells) in 4T1 (H and J) or MC38 (I and K) tumor. The results are presented as mean ± SEM. ∗p < 0.05 and ∗∗p < 0.01; NS, p > 0.05 (unpaired Student’s t test).