Figure 5.
Figure 5. Profile of responding T lymphocytes primed by stimulating DCs in allogeneic reactions. iDCs or IFN-β, IFN-λ, or LPS-treated DCs were used for 24 hours to stimulate allogeneic T-cell proliferation in vitro at a 1:10 DC/T-cell ratio. [3H]-Thymidine was added for the last 18 hours of culture. (A) CD4+ T lymphocytes present in MLR reactions were analyzed for their expression level of CD25 by flow cytometry. (B) Percentage of CD4+ CD25+hi T cells in MLR cultures. Mean ± SEM of 3 experiments performed with different blood donors. (C) Purity analysis of CD4+ T cells separated for the expression of CD25 by immunomagnetic selection into CD4+CD25– (i) and CD4+CD25+ T cells (ii). (D) Proliferation of CD4+CD25+ or CD25– T lymphocytes primed by DCs. Mean ± SEM of 3 independent experiments performed on different blood donors.

Profile of responding T lymphocytes primed by stimulating DCs in allogeneic reactions. iDCs or IFN-β, IFN-λ, or LPS-treated DCs were used for 24 hours to stimulate allogeneic T-cell proliferation in vitro at a 1:10 DC/T-cell ratio. [3H]-Thymidine was added for the last 18 hours of culture. (A) CD4+ T lymphocytes present in MLR reactions were analyzed for their expression level of CD25 by flow cytometry. (B) Percentage of CD4+ CD25+hi T cells in MLR cultures. Mean ± SEM of 3 experiments performed with different blood donors. (C) Purity analysis of CD4+ T cells separated for the expression of CD25 by immunomagnetic selection into CD4+CD25 (i) and CD4+CD25+ T cells (ii). (D) Proliferation of CD4+CD25+ or CD25 T lymphocytes primed by DCs. Mean ± SEM of 3 independent experiments performed on different blood donors.

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