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. 2020 Sep 28;218(1):e20181853. doi: 10.1084/jem.20181853

Figure S3.

Figure S3.

Transfer of T cells from Nfatc1deltaSUMO mice leads to less acute GvHD compared with WT T cells. (A) Preclinical model of aGvHD after MHC-mismatched allo-HCT. BALB/c (H-2d) mice were lethally irradiated with a single dose of 8.0 Gy and transplanted with 5 × 106 CD90.2+ BM cells and 1.2 × 106 CD90.1+ luc+ T cells from C57BL/6 donors (H-2b). (B) Body weight changes of host BALB/c mice (n = 5), irradiated (irradiation control) and transplanted with allogeneic BM (BM only), BM plus allogeneic WT (BM + WT), or BM plus allogeneic Nfatc1deltaSUMO (BM + ΔS) mice. (C) Representative in vivo BLI of mice transplanted with B6.CD90.2+ BM (BM only), BM plus B6.CD90.1+ luc+ WT T cells, and BM plus B6.CD90.1+ luc+ NFATc1/ΔS+ T cells. Statistical significance was calculated using two-way ANOVA; *, P < 0.05; ***, P < 0.001. (D) Frequency of splenic donor CD4+ and CD8+ T cells after 6 d, analyzed by flow cytometry and quantified from n = 15. (E) Analysis of serum IFN-γ and TNFα on days 2–6 after allo-HCT using cytometric bead array (n = 5, mean + SD).