Figure 3
Suppressive capacity segregates with the CD49d−CD127− CD4+ T-cell subset. (A) CD49d/CD127 FACS sorting. CD4+ cells isolated from PBMC with a commercial MACS-depletion kit were stained with α-CD49d and α-CD127 and sorted by FACS into the CD49d−CD127− and the CD49d+CD127− subset (top panels). The Foxp3 versus CD25 staining is shown in the bottom panels. Numbers represent percentages of cells per quadrant. (B) In vitro suppression assay. CD49d−CD127− and CD49d+CD127− cells were incubated with CD4+ cells. Proliferation of CD4+ cells was induced by stimulation; suppressor cells were added at a ratio of 1:1. Inhibition of the proliferative response of CD4+ cells was determined in a FACS-based suppression assay as shown in Figure 4B. Suppression is expressed as “% inhibition” based on the fraction of dividing cells in reference to noninhibited stimulated CD4+ cells. Summarized data of 4 independent experiments are shown (% inhibition CD49d−CD127− cells, 76.9% ± 12.8%; CD49d+CD127− cells, 27.8% ± 7%).

Suppressive capacity segregates with the CD49dCD127 CD4+ T-cell subset. (A) CD49d/CD127 FACS sorting. CD4+ cells isolated from PBMC with a commercial MACS-depletion kit were stained with α-CD49d and α-CD127 and sorted by FACS into the CD49dCD127 and the CD49d+CD127 subset (top panels). The Foxp3 versus CD25 staining is shown in the bottom panels. Numbers represent percentages of cells per quadrant. (B) In vitro suppression assay. CD49dCD127 and CD49d+CD127 cells were incubated with CD4+ cells. Proliferation of CD4+ cells was induced by stimulation; suppressor cells were added at a ratio of 1:1. Inhibition of the proliferative response of CD4+ cells was determined in a FACS-based suppression assay as shown in Figure 4B. Suppression is expressed as “% inhibition” based on the fraction of dividing cells in reference to noninhibited stimulated CD4+ cells. Summarized data of 4 independent experiments are shown (% inhibition CD49dCD127 cells, 76.9% ± 12.8%; CD49d+CD127 cells, 27.8% ± 7%).

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