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. Author manuscript; available in PMC: 2018 Nov 15.
Published in final edited form as: J Immunol. 2017 Oct 18;199(10):3700–3710. doi: 10.4049/jimmunol.1700380

Figure 1. T cell-derived CD70 inhibits inflammatory bowel disease (IBD).

Figure 1

(A) Naïve RAG1−/− mice in the C57BL/6 strain background were injected with 1×106 CD4+CD25 T cells purified from C57BL/6 WT or CD70−/− mice. Body weight was monitored after adoptive transfer. Representative weight data from 1 out of 3 independent experiments were shown as mean ± SD (n=4 per group), with statistical significance determined by two-way ANNOVA. (B) Kaplan-Meier survival data were summarized by combining 3 independent experiments (n=10–11 per group), with statistical significance determined by Log-rank test. (C-D) Naïve RAG1−/− mice were injected with 1×106 CD4+CD25 T cells purified from C57BL/6 WT mice, and then treated from day 1 with 100ug of either CD70 antibody (FR70) or IgG control twice weekly for the duration of the experiment. (C) Body weight was shown as mean ± SD, with statistical significance determined by two-way ANNOVA. (D) Kaplan-Meier survival curves were shown with statistical significance determined using Log-rank test. (E-F) RAG1−/− host mice were sacrificed on days 17, 36 and 66. A blinded pathologist scored large (E) and small (F) intestines based on disease criteria outline in the Experimental Procedures. Summary scores combined from 3 independent experiments were shown, with statistical significance determined by unpaired student t test. (G) Representative histopathological images were shown for large intestine samples harvested from RAG1−/− host mice at day 36 after adoptive transfer.