Figure 6.
IL-6 classical signaling in donor T cells drives Th22- and Th17-dependent GVHD. (A-L) Lethally irradiated (1300 cGy) B6D2F1 mice received BM and T cells or TCD BM allografts from control mice (CD4Cre− × IL-6Rfl) or mice with T cells deficient in IL-6 classical signaling (CD4Cre+ × IL-6Rfl). (B) Deletion of IL-6R on Cre+ recipients was confirmed by flow cytometric analysis of mIL-6R expression on peripheral blood CD4+ T cells before transplantation. (C) Functional confirmation was performed by stimulation of CD4+ T cells (in peripheral whole blood) with IL-6 (to induce classical signaling) or hyper–IL-6 (H-IL-6; to induce trans signaling) and upregulation of phosphorylated STAT3 (pSTAT3) expression measured by flow cytometry. (D) Survival indices by Kaplan-Meier analyses and weekly clinical GVHD scores of recipients after transplantation (BM and T-cell grafts, n = 12 mice per group; TCD, n = 6 mice per group; from 2 experiments). (E) Survival indices of recipient mice receiving grafts containing BM and the listed combination of sorted CD4+ (CD90.2+CD4+γδTCR−7AAD−) or CD8+ (CD90.2+CD4−γδTCR−7AAD−) T cells from CD4Cre− × IL-6Rfl (CD4 wild-type [CD4.WT] or CD8.WT) or CD4Cre+ × IL-6Rfl mice (T-cell grafts, n = 24 mice per group; TCD grafts, n = 8 mice per group; from 4 experiments). (F-I) CD4+ T-cell cytokine expression was assessed at day 7 after transplantation after stimulation. (F-G) Representative contour plots (mLNs; concatenated from 5 mice per group) (F) and frequencies of IFNγ, TNF, and GM-CSF expressing in CD4+ T cells isolated from the spleen and mLNs (n = 10 mice per group from 2 experiments) (G). (H-I) Representative flow cytometry plots of IL-22 and IL-17A in CD4+ T cells isolated from the mLNs (concatenated from 5 mice per group) (H) and frequencies and total numbers of Th22 (CD4+IL-22+IL-17−), IL-22+Th17 (CD4+IL-22+IL-17+), and IL-22−Th17 (CD4+IL-22−IL-17+) in the spleen, liver, mLNs, and peripheral LNs (pLNs) (n = 10 mice per group from 2 experiments) (I). (J) Peripheral blood serum levels of IL-17A at day 4 and day 7 after transplantation. (K-M) Frequency and total numbers of Tbet+ and RORγt+ in CD4+ T cells (K), Tr1 cells (CD4+IFNγ+IL-10+EOMES+) (L),73 and Tregs (CD4+FoxP3+) in the spleen at day 7 after transplantation (M) (n = 10 mice per group from 2 experiments). Data presented as mean ± standard error of the mean. *P < .05, **P < .01, ***P < .001. TBI, total-body irradiation.

IL-6 classical signaling in donor T cells drives Th22- and Th17-dependent GVHD. (A-L) Lethally irradiated (1300 cGy) B6D2F1 mice received BM and T cells or TCD BM allografts from control mice (CD4Cre × IL-6Rfl) or mice with T cells deficient in IL-6 classical signaling (CD4Cre+ × IL-6Rfl). (B) Deletion of IL-6R on Cre+ recipients was confirmed by flow cytometric analysis of mIL-6R expression on peripheral blood CD4+ T cells before transplantation. (C) Functional confirmation was performed by stimulation of CD4+ T cells (in peripheral whole blood) with IL-6 (to induce classical signaling) or hyper–IL-6 (H-IL-6; to induce trans signaling) and upregulation of phosphorylated STAT3 (pSTAT3) expression measured by flow cytometry. (D) Survival indices by Kaplan-Meier analyses and weekly clinical GVHD scores of recipients after transplantation (BM and T-cell grafts, n = 12 mice per group; TCD, n = 6 mice per group; from 2 experiments). (E) Survival indices of recipient mice receiving grafts containing BM and the listed combination of sorted CD4+ (CD90.2+CD4+γδTCR7AAD) or CD8+ (CD90.2+CD4γδTCR7AAD) T cells from CD4Cre × IL-6Rfl (CD4 wild-type [CD4.WT] or CD8.WT) or CD4Cre+ × IL-6Rfl mice (T-cell grafts, n = 24 mice per group; TCD grafts, n = 8 mice per group; from 4 experiments). (F-I) CD4+ T-cell cytokine expression was assessed at day 7 after transplantation after stimulation. (F-G) Representative contour plots (mLNs; concatenated from 5 mice per group) (F) and frequencies of IFNγ, TNF, and GM-CSF expressing in CD4+ T cells isolated from the spleen and mLNs (n = 10 mice per group from 2 experiments) (G). (H-I) Representative flow cytometry plots of IL-22 and IL-17A in CD4+ T cells isolated from the mLNs (concatenated from 5 mice per group) (H) and frequencies and total numbers of Th22 (CD4+IL-22+IL-17), IL-22+Th17 (CD4+IL-22+IL-17+), and IL-22Th17 (CD4+IL-22IL-17+) in the spleen, liver, mLNs, and peripheral LNs (pLNs) (n = 10 mice per group from 2 experiments) (I). (J) Peripheral blood serum levels of IL-17A at day 4 and day 7 after transplantation. (K-M) Frequency and total numbers of Tbet+ and RORγt+ in CD4+ T cells (K), Tr1 cells (CD4+IFNγ+IL-10+EOMES+) (L),73  and Tregs (CD4+FoxP3+) in the spleen at day 7 after transplantation (M) (n = 10 mice per group from 2 experiments). Data presented as mean ± standard error of the mean. *P < .05, **P < .01, ***P < .001. TBI, total-body irradiation.

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