Figure 7
Figure 7. Immune tolerance to cFVIII is associated with a cFVIII-expandable population of CD4+CD25+Foxp3+ T cells. (A) A representative flow cytometric analysis obtained with CD4+ T cells, derived from the spleens of hemophilia A mice that received Lenti-HCR/hAAT-cFVIII as neonates (cFIII-Tolerized) or did not receive gene transfer and were not challenged intravenously with cFVIII (Naive) and that were challenged with FVIII. Isolated splenocytes were stained directly (Pre-cFVIII) for CD4+CD25+Foxp3+ or after 72 hours in vitro stimulation with cFVIII (Post-cFVIII). (B) Comparison of the mean percentage of CD4+CD25+Foxp3+ T cells within the CD4+ cell population from the tolerized and naive mice before and after in vitro cFVIII stimulation. Error bars represent SEM, and * indicates a significant (P < .01) increase in CD4+CD25+Foxp3+ T cells.

Immune tolerance to cFVIII is associated with a cFVIII-expandable population of CD4+CD25+Foxp3+ T cells. (A) A representative flow cytometric analysis obtained with CD4+ T cells, derived from the spleens of hemophilia A mice that received Lenti-HCR/hAAT-cFVIII as neonates (cFIII-Tolerized) or did not receive gene transfer and were not challenged intravenously with cFVIII (Naive) and that were challenged with FVIII. Isolated splenocytes were stained directly (Pre-cFVIII) for CD4+CD25+Foxp3+ or after 72 hours in vitro stimulation with cFVIII (Post-cFVIII). (B) Comparison of the mean percentage of CD4+CD25+Foxp3+ T cells within the CD4+ cell population from the tolerized and naive mice before and after in vitro cFVIII stimulation. Error bars represent SEM, and * indicates a significant (P < .01) increase in CD4+CD25+Foxp3+ T cells.

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