Figure 4.
Figure 4. Polyclonal expansion of sorted CD4+CD25high T cells with bead-coupled anti-CD3/anti-CD28 Abs and high-dose IL-2. Sorted CD4+CD25high T cells can be expanded polyclonally with bead-coupled anti-CD3/anti-CD28 Abs and high-dose IL-2 without down-regulation of LN homing receptors or loss of suppressive function. (A) Sorted CD4+CD25high T cells (n = 7 individual cultures) were stimulated with anti-CD3/anti-CD28–coated beads plus IL-2. Symbols indicate different donors (n = 5; same as in Figure 2). (B) TCR Vβ-repertoire of CD4+CD25high and CD4+CD25- T cells before and after expansion for 24 days with Ab-coated beads and IL-2. One of 5 different cultures with cells from 5 different donors. (C) Surface expression of CD25, CD62L, CCR7, and CD27, and intracellular expression of CTLA-4 of CD4+CD25high T cells (gray histograms in i and ii; and iv and vi) and CD4+CD25- T cells (solid-line histograms in i and ii; and iii and v) after expansion with Ab-coated beads and IL-2 for 3 weeks. Dotted line indicates isotype control. Numbers indicate the percentage of cells within each quadrant. (D) CD4+ Tresp cells were stimulated with allogeneic PBMCs for 5 days. CD4+CD25high T cells, freshly isolated or expanded with Ab-coated beads for 13 or 22 days and then rested for 2 days, were added at variable numbers to obtain the indicated ratios. One of 3 independent experiments using cells from different donors. Error bars represent standard deviations from triplicate wells.

Polyclonal expansion of sorted CD4+CD25high T cells with bead-coupled anti-CD3/anti-CD28 Abs and high-dose IL-2. Sorted CD4+CD25high T cells can be expanded polyclonally with bead-coupled anti-CD3/anti-CD28 Abs and high-dose IL-2 without down-regulation of LN homing receptors or loss of suppressive function. (A) Sorted CD4+CD25high T cells (n = 7 individual cultures) were stimulated with anti-CD3/anti-CD28–coated beads plus IL-2. Symbols indicate different donors (n = 5; same as in Figure 2). (B) TCR Vβ-repertoire of CD4+CD25high and CD4+CD25- T cells before and after expansion for 24 days with Ab-coated beads and IL-2. One of 5 different cultures with cells from 5 different donors. (C) Surface expression of CD25, CD62L, CCR7, and CD27, and intracellular expression of CTLA-4 of CD4+CD25high T cells (gray histograms in i and ii; and iv and vi) and CD4+CD25- T cells (solid-line histograms in i and ii; and iii and v) after expansion with Ab-coated beads and IL-2 for 3 weeks. Dotted line indicates isotype control. Numbers indicate the percentage of cells within each quadrant. (D) CD4+ Tresp cells were stimulated with allogeneic PBMCs for 5 days. CD4+CD25high T cells, freshly isolated or expanded with Ab-coated beads for 13 or 22 days and then rested for 2 days, were added at variable numbers to obtain the indicated ratios. One of 3 independent experiments using cells from different donors. Error bars represent standard deviations from triplicate wells.

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