Figure 6.
Figure 6. ILT3 is dispensable for induction of CD4+Foxp3+ regulatory T cells by 1,25(OH)2D3-treated DCs. The read-out system to test for suppressive activity was composed of CFSE-labeled CD4+CD25-cells from donor A PBMCs cultured with 1:10 LPS-matured monocyte-derived DCs from donor B in the presence of 1 μg/mL anti–human CD3 mAb. To evaluate the induction of Ts, CD4+ T cells from donor C were generated by 3 rounds of restimulation with allogeneic immature monocyte-derived DCs from donor D, which were cultured for the last 48 hours with or without 10 nM 1,25(OH)2D3. The coculture was carried out with or without anti-ILT3 mAb (20 μg/mL). After 96 hours of culture, cells were analyzed by flow cytometry. Expression of Foxp3 transcripts, evaluated by real time RT-PCR, is shown as arbitrary units (AU) normalized to GAPDH signals. (A) Proliferation of CFSE-labeled CD4+CD25– cells (5 × 104/well). Basal levels of Foxp3 transcripts are expressed as AU. (B) Addition of blood CD4+CD25+ cells (6.5 × 103/well) inhibits CD4+CD25– cell proliferation. Foxp3 expression of blood CD4+CD25+ cells is indicated. (C) CD4+ cells (6.5 × 103/well) stimulated for 3 rounds with allogeneic immature monocyte-derived DCs (CD4-iDC) show enhanced Foxp3 expression and inhibit proliferation of CFSE-labeled CD4+CD25– cells. (D) CD4+ cells stimulated for 3 rounds with allogeneic immature monocyte-derived DCs in the presence of 10 nM 1,25(OH)2D3 (CD4-iDC-D3) show enhanced Foxp3 expression and inhibit proliferation of CFSE-labeled CD4+CD25– cells. (E) Addition of anti-ILT3 mAb to CD4+ cells stimulated for 3 rounds with allogeneic immature monocyte-derived DCs (CD4-iDC-αILT3) show basal levels of Foxp3 expression and fail to inhibit proliferation of CFSE-labeled CD4+CD25– cells. (F) Addition of anti-ILT3 mAb to CD4+ cells stimulated for 3 rounds with allogeneic immature monocyte-derived DCs in the presence of 10 nM 1,25(OH)2D3 (CD4-iDC-D3-αILT3) show enhanced Foxp3 expression and inhibit proliferation of CFSE-labeled CD4+CD25– cells. A representative experiment out of 2 performed is shown.

ILT3 is dispensable for induction of CD4+Foxp3+ regulatory T cells by 1,25(OH)2D3-treated DCs. The read-out system to test for suppressive activity was composed of CFSE-labeled CD4+CD25-cells from donor A PBMCs cultured with 1:10 LPS-matured monocyte-derived DCs from donor B in the presence of 1 μg/mL anti–human CD3 mAb. To evaluate the induction of Ts, CD4+ T cells from donor C were generated by 3 rounds of restimulation with allogeneic immature monocyte-derived DCs from donor D, which were cultured for the last 48 hours with or without 10 nM 1,25(OH)2D3. The coculture was carried out with or without anti-ILT3 mAb (20 μg/mL). After 96 hours of culture, cells were analyzed by flow cytometry. Expression of Foxp3 transcripts, evaluated by real time RT-PCR, is shown as arbitrary units (AU) normalized to GAPDH signals. (A) Proliferation of CFSE-labeled CD4+CD25 cells (5 × 104/well). Basal levels of Foxp3 transcripts are expressed as AU. (B) Addition of blood CD4+CD25+ cells (6.5 × 103/well) inhibits CD4+CD25 cell proliferation. Foxp3 expression of blood CD4+CD25+ cells is indicated. (C) CD4+ cells (6.5 × 103/well) stimulated for 3 rounds with allogeneic immature monocyte-derived DCs (CD4-iDC) show enhanced Foxp3 expression and inhibit proliferation of CFSE-labeled CD4+CD25 cells. (D) CD4+ cells stimulated for 3 rounds with allogeneic immature monocyte-derived DCs in the presence of 10 nM 1,25(OH)2D3 (CD4-iDC-D3) show enhanced Foxp3 expression and inhibit proliferation of CFSE-labeled CD4+CD25 cells. (E) Addition of anti-ILT3 mAb to CD4+ cells stimulated for 3 rounds with allogeneic immature monocyte-derived DCs (CD4-iDC-αILT3) show basal levels of Foxp3 expression and fail to inhibit proliferation of CFSE-labeled CD4+CD25 cells. (F) Addition of anti-ILT3 mAb to CD4+ cells stimulated for 3 rounds with allogeneic immature monocyte-derived DCs in the presence of 10 nM 1,25(OH)2D3 (CD4-iDC-D3-αILT3) show enhanced Foxp3 expression and inhibit proliferation of CFSE-labeled CD4+CD25 cells. A representative experiment out of 2 performed is shown.

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