Differential expression and modulation of costimulatory molecules CD80 andCD86 on monocytes from patients with systemic lupus erythematosus

Citation
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
Citations number
23
Categorie Soggetti
Immunology
Journal title
SCANDINAVIAN JOURNAL OF IMMUNOLOGY
ISSN journal
03009475 → ACNP
Volume
49
Issue
1
Year of publication
1999
Pages
82 - 87
Database
ISI
SICI code
0300-9475(199901)49:1<82:DEAMOC>2.0.ZU;2-D
Abstract
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.