Table 1

Immunophenotype of iDCZol+ and mDCZol+

iDCZol−*iDCZol+mDCZol−mDCZol+
HLA-DR 680 ± 283 622 ± 249 1.287 ± 586 1.698 ± 910 
CD86 78 ± 25 142 ± 55 113 ± 30 121 ± 30 
CD80 235 ± 57 246 ± 55 263 ± 57 349 ± 85 
CD54 1.617 ± 341 1.685 ± 487 2.219 ± 780 2.168 ± 520 
CD83 82 ± 23 59 ± 15 139 ± 69 121 ± 46 
CD11a 116 ± 58 113 ± 55 121 ± 48 619 ± 517 
CCR7 367 ± 35 368 ± 13 356 ± 36 317 ± 25 
CXCR4 132 ± 58 128 ± 57 136 ± 66 136 ± 72 
DC-LAMP 58 ± 2 54 ± 5 78 ± 10 88 ± 2 
iDCZol−*iDCZol+mDCZol−mDCZol+
HLA-DR 680 ± 283 622 ± 249 1.287 ± 586 1.698 ± 910 
CD86 78 ± 25 142 ± 55 113 ± 30 121 ± 30 
CD80 235 ± 57 246 ± 55 263 ± 57 349 ± 85 
CD54 1.617 ± 341 1.685 ± 487 2.219 ± 780 2.168 ± 520 
CD83 82 ± 23 59 ± 15 139 ± 69 121 ± 46 
CD11a 116 ± 58 113 ± 55 121 ± 48 619 ± 517 
CCR7 367 ± 35 368 ± 13 356 ± 36 317 ± 25 
CXCR4 132 ± 58 128 ± 57 136 ± 66 136 ± 72 
DC-LAMP 58 ± 2 54 ± 5 78 ± 10 88 ± 2 

Results are mean fluorescence intensity (MFI) plus or minus the SEM from 10 (HLA-DR) to 3 (DC-LAMP) experiments.

*

iDCs were generated from peripheral monocytes by incubation for 6 days with IL-4 and granulocyte-macrophage colony-stimulating factor as reported in “Materials and methods.” On day 6, iDCs were harvested and incubated for 24 hours in the presence (iDCZol+) or absence of 5 μM Zol (iDCZol−).

mDCs were generated by incubation of iDCs with TNF-α and IL-1β for 24 hours in the presence (mDCZol+) or absence (mDCZol−) of 5 μM Zol. DC-LAMP expression is determined after 48 hours of incubation.

Difference statistically significant between mDCZol− and mDCZol+ (both P < .05).

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