CD4+ T-cell responses in primary culture
. | Control T cells . | G-CSF T cells . | ProGP-1 T cells . |
---|---|---|---|
Cpm | 72.5 ± 4.6 | 55.8 ± 4.2 | 61.6 ± 4.8 |
IFNγ | 31.1 ± 3.1 | 37.5 ± 3.5 | 35.7 ± 1.1 |
IL-4 | 523 ± 34 | 2064 ± 81* | 1221 ± 120* |
IL-10 | 383 ± 191 | 917 ± 72* | 935 ± 145* |
. | Control T cells . | G-CSF T cells . | ProGP-1 T cells . |
---|---|---|---|
Cpm | 72.5 ± 4.6 | 55.8 ± 4.2 | 61.6 ± 4.8 |
IFNγ | 31.1 ± 3.1 | 37.5 ± 3.5 | 35.7 ± 1.1 |
IL-4 | 523 ± 34 | 2064 ± 81* | 1221 ± 120* |
IL-10 | 383 ± 191 | 917 ± 72* | 935 ± 145* |
Naive B6 (H2b) mice received control diluent, G-CSF, or ProGP-1 as described in “Materials and methods.” Splenic CD4+ T cells were purified by magnetic separation or FACS (as described in “Materials and methods”) and stimulated in primary culture by plate-bound antibodies to CD3 and CD28 (both at 10 μg/mL). Results represent mean ± SE of triplicate wells.
P < .05 versus control T cells. Proliferative responses (×103) were measured by 3H incorporation. IFNγ (U/mL), IL-4 (pg/mL), and IL-10 (pg/mL) were determined in culture supernatants by ELISA.