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. 2014 Aug 18;124(13):2131–2141. doi: 10.1182/blood-2013-10-525873

Figure 2.

Figure 2

In vivo ablation of donor Foxp3+ T cells abolishes PTCy protection against GVHD. (A) Experimental schema. BALB/B recipients after lethal conditioning (775 cGy) received 107 TCD BM (B6 CD45.1+) and GVH inocula of 12 × 106 splenocytes and CLN cells from Foxp3DTR or Foxp3WT B6 CD45.2+ donors. Designated groups received DT (50 ng/g IP) or PBS on days 0 and +1. PTCy (200 mg/kg IP) was administered to designated groups on day +3 post-alloBMT. All animals were monitored daily for survival and scored twice weekly for GVHD on day +7 post-alloBMT and every 4 days thereafter until day +60, when experiments were terminated. (B) Mean GVHD scores and survival. Combined results of 3 independent experiments are shown. (C) Frequency of cytokine-producing, inocula-derived CD4+CD45.2+ T cells in spleens of surviving chimeras on day +28. (D) Frequency (left panel) and total numbers (right panel) of CD4+CD45.2+Foxp3+ T cells in the spleens of surviving chimeras on day +28. Data are representative of 3 independent experiments, with a minimum of 4 animals per group. The results are presented as the mean ± standard error of the mean.