Figure 4
Figure 4. Tregs expanded with DCs from CTX-treated mice have less suppressor activity. Isolated CD4+ CD25+ Tregs from Balb/c mice were cocultured with different DC subsets (DCs from naive mice, DCs from CTX-treated mice, CD8+ DCs, and DCs from CTX-treated mice + CD8+ DCs) from B6 mice (primary MLR). After 7 days, Tregs expanded with different DC subsets were mixed with 105 CFSE-labeled CD25− CD3+ T cells in various ratios (2:1-32:1) and stimulated with irradiated mature DCs activated with LPS (secondary MLR). At 5 days after secondary MLR culture, T-cell proliferation was examined by measurement of CFSE dilution. Results are the mean ± SEM of triplicate wells. Data are representative of 2 independent experiments. *Statistically significant.

Tregs expanded with DCs from CTX-treated mice have less suppressor activity. Isolated CD4+ CD25+ Tregs from Balb/c mice were cocultured with different DC subsets (DCs from naive mice, DCs from CTX-treated mice, CD8+ DCs, and DCs from CTX-treated mice + CD8+ DCs) from B6 mice (primary MLR). After 7 days, Tregs expanded with different DC subsets were mixed with 105 CFSE-labeled CD25 CD3+ T cells in various ratios (2:1-32:1) and stimulated with irradiated mature DCs activated with LPS (secondary MLR). At 5 days after secondary MLR culture, T-cell proliferation was examined by measurement of CFSE dilution. Results are the mean ± SEM of triplicate wells. Data are representative of 2 independent experiments. *Statistically significant.

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