Fig. 4.
Fig. 4. Characterization of the CD4+ T-cell response to MAGE-3161-175. / CD4+ T cells from donor/patient 5 (HLA-DR4, HLA-DR11) were propagated by weekly restimulation with pool II. (A) Proliferative responses, measured in 2-day microproliferation assays, to each single peptide forming pool II (10 μg/mL) after 5 weeks of propagation of the line. The blank (ie, the basal level of proliferation of CD4+ T cells in the presence of homozygous PBMCs or LCLs as APCs) is expressed as B + DR11-PBMC or B + DR4-LCL. (B) Proliferative responses to each single peptide forming pool II (10 μg/mL) after magnetic selection of MAGE-3161-175–specific CD4+ T cells. (C) IFN-γ release of CD4+ T cells in the presence of melanoma cells, DR4-LCL, MAGE-3161-175–pulsed DR4-LCL, DR4-LCL-M3, and DR4-LCL-IiM3. The data shown in panels A to C are means of triplicate determinations ± SDs. Responses significantly higher than the blanks are indicated: **.001 < P < .05, ***P < .001 (determined by unpaired, one-tailed Student ttest).

Characterization of the CD4+ T-cell response to MAGE-3161-175.

CD4+ T cells from donor/patient 5 (HLA-DR4, HLA-DR11) were propagated by weekly restimulation with pool II. (A) Proliferative responses, measured in 2-day microproliferation assays, to each single peptide forming pool II (10 μg/mL) after 5 weeks of propagation of the line. The blank (ie, the basal level of proliferation of CD4+ T cells in the presence of homozygous PBMCs or LCLs as APCs) is expressed as B + DR11-PBMC or B + DR4-LCL. (B) Proliferative responses to each single peptide forming pool II (10 μg/mL) after magnetic selection of MAGE-3161-175–specific CD4+ T cells. (C) IFN-γ release of CD4+ T cells in the presence of melanoma cells, DR4-LCL, MAGE-3161-175–pulsed DR4-LCL, DR4-LCL-M3, and DR4-LCL-IiM3. The data shown in panels A to C are means of triplicate determinations ± SDs. Responses significantly higher than the blanks are indicated: **.001 < P < .05, ***P < .001 (determined by unpaired, one-tailed Student ttest).

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