Figure 2
Figure 2. Duration of in vitro programming stimulus is a critical determinant of in vivo antitumor efficacy. (A) Sublethally irradiated WT mice bearing day 10 established subcutaneous B16 tumors were left untreated as controls (×) or received pmel TEM cells (●), pmel TEM cells programmed in vitro with 1 μM hgp10025-33 peptide-pulsed irradiated APCs for indicated time points before transfer (■), or pmel TEM cells plus rFPgp100 vaccination (□). For groups receiving pmel TEM cells, mice received 106 cells. For mice receiving peptide-programmed pmel TEM cells, cultures were started with 106 cells, and the total number of cells present at the time of transfer was divided evenly between the numbers of recipient mice and transferred. For all treatment groups receiving cell transfer, mice also received exogenous rhIL-2 (36 μg/dose × 6 doses). Results for tumor treatment experiments are presented as the mean measurements from 5 mice per group (± SEM). (B) Increased duration of in vitro programming does not impair the relative efficiency of engraftment after adoptive cell transfer. pmel TEM cells were transferred without further stimulation (■) or received programming with 1 μM hgp10025-33 peptide-pulsed irradiated APCs for 24 hours (▩) or 72 hours (□) before ACT. For all groups, cultures were started with 107 pmel TEM cells, and the total number of cells present at the time of transfer were divided evenly between recipient mice and transferred. The absolute number of pmel cells (identified by CD8+tetramer+ lymphocytes) was enumerated in the spleen of recipient mice 48 hours after transfer as outlined in “In vivo tumor treatment and enumeration of adoptively transferred cells.” Each data point represents the average ± SEM of 3 independent mice per treatment group. This experiment was repeated twice with similar results. *P < .01 for the comparisons of nonstimulated pmel TEM cells and TEM cells programmed for 24 hours to TEM cells programmed for 72 hours before transfer. †P > .2 for the comparison of nonstimulated pmel TEM cells to TEM cells programmed for 24 hours before transfer.

Duration of in vitro programming stimulus is a critical determinant of in vivo antitumor efficacy. (A) Sublethally irradiated WT mice bearing day 10 established subcutaneous B16 tumors were left untreated as controls (×) or received pmel TEM cells (●), pmel TEM cells programmed in vitro with 1 μM hgp10025-33 peptide-pulsed irradiated APCs for indicated time points before transfer (■), or pmel TEM cells plus rFPgp100 vaccination (□). For groups receiving pmel TEM cells, mice received 106 cells. For mice receiving peptide-programmed pmel TEM cells, cultures were started with 106 cells, and the total number of cells present at the time of transfer was divided evenly between the numbers of recipient mice and transferred. For all treatment groups receiving cell transfer, mice also received exogenous rhIL-2 (36 μg/dose × 6 doses). Results for tumor treatment experiments are presented as the mean measurements from 5 mice per group (± SEM). (B) Increased duration of in vitro programming does not impair the relative efficiency of engraftment after adoptive cell transfer. pmel TEM cells were transferred without further stimulation (■) or received programming with 1 μM hgp10025-33 peptide-pulsed irradiated APCs for 24 hours (▩) or 72 hours (□) before ACT. For all groups, cultures were started with 107 pmel TEM cells, and the total number of cells present at the time of transfer were divided evenly between recipient mice and transferred. The absolute number of pmel cells (identified by CD8+tetramer+ lymphocytes) was enumerated in the spleen of recipient mice 48 hours after transfer as outlined in “In vivo tumor treatment and enumeration of adoptively transferred cells.” Each data point represents the average ± SEM of 3 independent mice per treatment group. This experiment was repeated twice with similar results. *P < .01 for the comparisons of nonstimulated pmel TEM cells and TEM cells programmed for 24 hours to TEM cells programmed for 72 hours before transfer. †P > .2 for the comparison of nonstimulated pmel TEM cells to TEM cells programmed for 24 hours before transfer.

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