TABLE 3.
TCM inhibits LPS-induced HLA-DR and CD40 up-regulationa
Condition(s) | Surface molecule expression (MFI)b
|
||||
---|---|---|---|---|---|
HLA-DR | CD40 | CD54 | CD80 | CD86 | |
Medium | 216 ± 3 | 55 ± 4 | 84 ± 31 | 21 ± 5 | 33 ± 16 |
Medium + TCM | 232 ± 41 | 46 ± 4 | 55 ± 19 | 19 ± 5 | 33 ± 16 |
LPS | 1,006 ± 419 | 99 ± 11 | 125 ± 35 | 45 ± 6 | 106 ± 20 |
LPS + TCM | 680 ± 244* | 72 ± 9* | 114 ± 26 | 35 ± 4 | 72 ± 4 |
DC were stimulated with LPS (10 ng/ml) in the presence or absence of TCM (75%). After 2 h, the DC were harvested and washed, and the expression of surface molecules was determined by flow cytometry analysis. As a control, DC were incubated in medium alone in the presence or the absence of TCM (75%).
Results are expressed as median fluorescence intensity (MFI) and represent the mean ± standard error of the mean of six independent experiments with six different donors. Cell labeling with control MAb was not affected by TCM (data not shown). *, P ≤ 0.01 by nonparametric Wilcoxon’s paired one-tailed test, compared to MFI in the absence of TCM.