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Circulating T cells from healthy volunteers ( n = 6), depleted or not for regulatory T cells, were co-cultured with circulating PCs purified from septic patients ( n = 6) at 1:1 ratio for 72 h and stimulated by anti-CD2/CD3/CD28 antibodies-coated beads. Proliferation of CD3+ T cells was measured among viable cells by flow cytometry. Geometric means with standard deviations (SD) and individual values are shown. Two-sided Wilcoxon paired tests were used to compare results of T-cell proliferation between culture conditions. Only significant p values < 0.05 are shown.

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