Mf. Liu et al., Differential expression and modulation of costimulatory molecules CD80 andCD86 on monocytes from patients with systemic lupus erythematosus, SC J IMMUN, 49(1), 1999, pp. 82-87
Patients with systemic lupus erythematosus (SLE) were recently shown to be
defective in costimulatory molecule CD80 (B7-1) expression on antigen-prese
nting cells. This study was undertaken to further investigate the expressio
n and cytokine regulation of both CD80 and CD86 (B7-2) on monocytes from pa
tients with SLE. Freshly isolated and in vitro cytokine-stimulated peripher
al blood mononuclear cells from 13 patients with SLE and 10 healthy subject
s were analysed, cytometrically with dual-fluorescence staining, to detect
expression of CD80 and CD86 in the CD14(+) monocyte population. The results
showed that, as in normal individuals, an overwhelming majority (95.62 +/-
3.54%) of monocytes from patients with SLE expressed the CD86 molecule, bu
t only a few monocytes (5.54 +/- 4.36%) had detectable CD80 expression. The
effects of interleukin-10 (IL-10) on the expression of CD80 and CD86 on mo
nocytes from patients with SLE and normal controls were similar. IL-10 down
-regulated the expression of CD86 while it slightly enhanced that of CD80.
Interferon-gamma (IFN-gamma) increased both CD80 and CD86 expression on mon
ocytes from both SLE patients and normal groups, albeit less significantly
in the former than in the latter, i.e. CD80: 142.84 +/- 65.99% versus 226.0
8 +/- 78.90%, P < 0.05; and CD86: 72.55 +/- 74.23% versus 153.99 +/- 94.14%
, P<0.05, when expressed as percentage modulation. Granulocyte-macrophage c
olony-stimulating factor (GM-CSF) showed a capacity for up-regulation of CD
80 and CD86 expression on monocytes, of a magnitude that was similar both i
n patients with SLE and in normal subjects. We concluded that CD80 and CD86
were differentially expressed and modulated on monocytes and the defective
IFN-gamma-induced up-regulation of CD80 and CD86 expression on SLE monocyt
es might be a factor in the pathogenesis of SLE.