Table 3.

Phenotype analysis of DCs matured after exposure to LPS in the presence of IVIg

TreatmentCD83HLA-DRCD86CD80CD40CD95
Ctl-LPS 30 ± 2 208 ± 32 84 ± 16 53 ± 7 381 ± 34 46 ± 9 
IVIg-LPS 21 ± 43-150 156 ± 50 54 ± 103-150 40 ± 43-150 210 ± 326 34 ± 10 
HSA-LPS 29 ± 4 173 ± 12 111 ± 4 56 ± 5 404 ± 156 46 ± 2 
TreatmentCD83HLA-DRCD86CD80CD40CD95
Ctl-LPS 30 ± 2 208 ± 32 84 ± 16 53 ± 7 381 ± 34 46 ± 9 
IVIg-LPS 21 ± 43-150 156 ± 50 54 ± 103-150 40 ± 43-150 210 ± 326 34 ± 10 
HSA-LPS 29 ± 4 173 ± 12 111 ± 4 56 ± 5 404 ± 156 46 ± 2 

Immature DCs obtained after 5-day culture with IL-4 and GM-CSF were treated with IVIg (0.15 mM) for 12 hours followed by stimulation with LPS (1 μg/mL) (IVIg-LPS) or were treated with LPS alone (Ctl-LPS) for 48 hours. In control experiments, cells were treated with HSA, an irrelevant protein, for 12 hours followed by stimulation with LPS (HSA-LPS). Results are expressed as MFI. Data are from 4 independent experiments from different donors. Statistical significance as determined by unpaired Student t test is indicated.

F3-150

P < .05.

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