Table 3.

IFN-γ does not shift immature DCs toward macrophages

No
cytokine
GM-CSF + IL-4
NoneIFN-γIFN-γ +
M-CSF
M-CSF +
IL-6
CD1153-150 ND 76 ± 10 83 ± 13 10 ± 3 15 ± 2 
CD1a3-151 11 ± 2 310 ± 35 298 ± 29 358 ± 42 399 ± 50 
CD143-151 56 ± 9 < 5 < 5 < 5 < 5 
CD833-152 < 5% 99% 98% 99% 99% 
MLR3-153 ND 2 ± 0.1 5 ± 0.8 ND ND 
MLR3-155 ND 22 ± 2 24 ± 3 ND ND 
No
cytokine
GM-CSF + IL-4
NoneIFN-γIFN-γ +
M-CSF
M-CSF +
IL-6
CD1153-150 ND 76 ± 10 83 ± 13 10 ± 3 15 ± 2 
CD1a3-151 11 ± 2 310 ± 35 298 ± 29 358 ± 42 399 ± 50 
CD143-151 56 ± 9 < 5 < 5 < 5 < 5 
CD833-152 < 5% 99% 98% 99% 99% 
MLR3-153 ND 2 ± 0.1 5 ± 0.8 ND ND 
MLR3-155 ND 22 ± 2 24 ± 3 ND ND 

Day 5 immature DCs were cultured in the absence of cytokine or in GM-CSF plus IL-4 in the absence or presence of 25 ng/mL IFN-γ, 25 ng/mL IFN-γ plus 100 ng/mL M-CSF, or 100 ng/mL M-CSF plus 100 ng/mL IL-6.

ND indicates not done.

F3-150

After 1 day, membrane CD115 expression was analyzed by FACS.

F3-151

After 3 days, CD1a and CD14 expression were analyzed by FACS. For CD1a, CD14, and CD115, results are expressed in MFI ± values, mean SD of 4 separate experiments.

F3-152

After 3 days, cells were further stimulated for 24 hours with LPS, and CD83 was analyzed by FACS. Results are expressed in percentage of positive cells.

F3-153

After 2 days, cells were used as stimulatory cells in primary allogeneic MLRs.

F3-155

After 2 days, cells were stimulated for 24 hours with LPS before being used as stimulatory cells in primary allogeneic MLRs. Results are expressed in counts per minute × 10−3 as mean ± SD of quadruplicate values and are representative of 1 of 3 experiments.

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