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. 2019 Jul 11;178(2):346–360.e24. doi: 10.1016/j.cell.2019.05.047

Figure 3.

Figure 3

Neutrophils Drive DNTαβ Type 1 Polarization

(A) Expression of IFNγ by tumor-infiltrating T cells stimulated ex vivo by PMA plus ionomycin.

(B) Representative dot plot showing Rorγt, and T-bet expression in UTCαβ from Csf3r+/+ and Csf3r−/− tumors.

(C and D) Quantification of Eomes, Rorγt, and T-bet expression in UTCαβ from Csf3r+/+ and Csf3r−/− tumors (C) and in Csf3r−/− mice after adoptive transfer of neutrophils (D).

(E) Expression of Eomes, Rorγt, and T-bet in UTCαβ infiltrating the 3-MCA injection site (10 days after administration of 3-MCA).

(F) Quantification of iNKT, MAIT, and DNTαβ frequencies among sarcoma-infiltrating CD45+ cells.

(G) Polarization of tumor-associated DNTαβ cells after neutrophil adoptive transfer.

(D and G) 3 × 106 neutrophils were transferred i.v. once a week starting from the first day the tumor was palpable. (E) 3 × 106 neutrophils were transferred i.v. at days −1, 0, 1, and 9 with respect to 3-MCA administration. (A and C–G) Data are mean ± SEM. p ≤ 0.05, ∗∗p ≤ 0.01, ∗∗∗p ≤ 0.001. (A, C, and F) Two-tailed multiple Student’s t tests. (D) One-way ANOVA. (E and G) Kruskal-Wallis test with Dunn’s multiple comparison test.

See also Figures S3 and S4.