Table 3.

Activation of Clonal T Cells From Patient 2 by DC Requires Addition of rIL-2

MLC Conditions3-150Apoptotic Cells (%)3H-Thymidine Uptake (cpm) IL-5 (pg/mL)IL-13 (pg/mL) IFN-γ (U/mL)
T cells  54  47 <20  <10  <2  
T cells + DC  51  143 <20  <10  <2  
T cells + rIL-2  28  22,886 502  427  <2  
T cells + DC + rIL-2  24  35,010 32,520  11,100  <2 
MLC Conditions3-150Apoptotic Cells (%)3H-Thymidine Uptake (cpm) IL-5 (pg/mL)IL-13 (pg/mL) IFN-γ (U/mL)
T cells  54  47 <20  <10  <2  
T cells + DC  51  143 <20  <10  <2  
T cells + rIL-2  28  22,886 502  427  <2  
T cells + DC + rIL-2  24  35,010 32,520  11,100  <2 
F3-150

Purified CD3CD4+ cells from patient 2 were cocultured with mature irradiated DC generated from allogeneic PBMC (DC:T-cell ratio 1:30) in absence or in the presence of rIL-2 (150 U/mL). After 5 days, the percentage of apoptotic cells was determined by flow cytometry using annexin V and PI staining, T-cell proliferation was determined by 3H-thymidine uptake, and cytokine concentrations were measured in supernatants by ELISA. Data are from 1 of 8 experiments, which gave similar results.

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