Figure 3
Figure 3. On day 19 after BMT without vaccination, KGF does not change the percentage of CD8+tetramer+ cells that could respond to vaccination or the percentage of CD4+ cells that express Foxp3 but does increase the overall number CD8+tetramer+ and CD4+Foxp3+ cells in each mouse. B6 mice underwent T cell-depleted BMT and were treated with KGF as described in Figure 1. On day 19, frequency and total number of CD8+tetramer+ cells were determined by purifying peripheral CD8+ cells (combined spleens and inguinal LNs) with magnetic beads, and staining with opt-TRP1-455 tetramer. Purified CD8+ cells staining for tetramer (A and B, *P = .004) and splenocytes staining for Foxp3 (C,D, *P < .001) were analyzed with flow cytometry. Data are pooled from 2 experiments with similar results.

On day 19 after BMT without vaccination, KGF does not change the percentage of CD8+tetramer+ cells that could respond to vaccination or the percentage of CD4+ cells that express Foxp3 but does increase the overall number CD8+tetramer+ and CD4+Foxp3+ cells in each mouse. B6 mice underwent T cell-depleted BMT and were treated with KGF as described in Figure 1. On day 19, frequency and total number of CD8+tetramer+ cells were determined by purifying peripheral CD8+ cells (combined spleens and inguinal LNs) with magnetic beads, and staining with opt-TRP1-455 tetramer. Purified CD8+ cells staining for tetramer (A and B, *P = .004) and splenocytes staining for Foxp3 (C,D, *P < .001) were analyzed with flow cytometry. Data are pooled from 2 experiments with similar results.

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