Figure 6
TLR stimulation and CD4 help license DC to prime CD8+ T cells. (A-B) Autologous naive CD4+ or CD8+ T cells from peripheral blood were CFSE-labeled and cultured alone or together with allogeneic DC or monocytes subsets in the absence (−) or presence of TLR agonists as indicated. Proliferation was assessed after 7 days by CFSE dilution and is shown as the percentage of divided CD4+ T cells (A) or CD8+ T cells (B). (C) MHC class I (upper panels) and CD86 (lower panels) expression on DC before (filled histograms) or after stimulation (open histograms) with LPS + R848 of mDC1 (left panels), with polyI:C + R848 of mDC2 (central panels) and with CpG of pDC (right panels). One representative donor of 3 is shown. *P < .05; **P < .005; ***P < .0005.

TLR stimulation and CD4 help license DC to prime CD8+ T cells. (A-B) Autologous naive CD4+ or CD8+ T cells from peripheral blood were CFSE-labeled and cultured alone or together with allogeneic DC or monocytes subsets in the absence (−) or presence of TLR agonists as indicated. Proliferation was assessed after 7 days by CFSE dilution and is shown as the percentage of divided CD4+ T cells (A) or CD8+ T cells (B). (C) MHC class I (upper panels) and CD86 (lower panels) expression on DC before (filled histograms) or after stimulation (open histograms) with LPS + R848 of mDC1 (left panels), with polyI:C + R848 of mDC2 (central panels) and with CpG of pDC (right panels). One representative donor of 3 is shown. *P < .05; **P < .005; ***P < .0005.

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