Figure 1.
Human T-cell differentiation in ND samples and patients with early T-cell block. (A) Representative analysis of T-cell differentiation in an ND sample at 8 weeks (ND4). Cells were gated on LIVE/DEAD–CD45+CD14–CD56– cells to check for the presence of CD34+ and CD19+ cells and the expression of early and late T-cell commitment markers (CD5, CD7, CD1a, CD4, CD8α, CD8β, CD3, TCRαβ, and TCRγδ). (B-D) T-cell differentiation assay in patients with reticular dysgenesis (RD) (analyzed at 5 weeks) (B), and XSCID, carrying a null (P2) (6 weeks) (C), or a missense mutation (P3) (6 weeks) (D). The fluorescence-activated cell sorting (FACS) plots show expression of CD34, CD19, CD7, CD5, CD1a, CD4, CD8β, TCRαβ, and CD3 upon gating on LIVE/DEAD–CD45+CD14–CD56– cells. CD5, CD7, and CD1a plots are obtained upon gating on LIVE/DEAD–CD45+CD14–CD56–CD34– cells. The bar graphs show the absolute cell counts per ATO in the indicated gates in each patient’s sample and in the ND sample (red bars) analyzed in parallel in the T-cell differentiation assay.

Human T-cell differentiation in ND samples and patients with early T-cell block. (A) Representative analysis of T-cell differentiation in an ND sample at 8 weeks (ND4). Cells were gated on LIVE/DEADCD45+CD14CD56 cells to check for the presence of CD34+ and CD19+ cells and the expression of early and late T-cell commitment markers (CD5, CD7, CD1a, CD4, CD8α, CD8β, CD3, TCRαβ, and TCRγδ). (B-D) T-cell differentiation assay in patients with reticular dysgenesis (RD) (analyzed at 5 weeks) (B), and XSCID, carrying a null (P2) (6 weeks) (C), or a missense mutation (P3) (6 weeks) (D). The fluorescence-activated cell sorting (FACS) plots show expression of CD34, CD19, CD7, CD5, CD1a, CD4, CD8β, TCRαβ, and CD3 upon gating on LIVE/DEADCD45+CD14CD56 cells. CD5, CD7, and CD1a plots are obtained upon gating on LIVE/DEADCD45+CD14CD56CD34 cells. The bar graphs show the absolute cell counts per ATO in the indicated gates in each patient’s sample and in the ND sample (red bars) analyzed in parallel in the T-cell differentiation assay.

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