Objective
T cell abnormalities, B cell hyperactivity and abnormal cytokine production
have been implicated to be of pathogenic importance in systemic lupus eryt
hematosus (SLE). The aim of this study was to investigate if ongoing produc
tion and serum levels of type 1 and 2 cytokines reflect disease activity an
d the presence of organ manifestations.
Methods
Fifty-two SLE patients and 29 healthy individuals were investigated. Blood
samples were collected for assessment of anti-ds DNA antibodies, cytokine p
roduction and serum cytokine levels. Disease activity was simultaneously as
sessed using the Systemic Lupus Activity Measure (SLAM) index and SLE Disea
se Activity Index (SLEDAI). ELISPOT analysis of freshly isolated peripheral
blood mononuclear cells (PBMC) was used to estimate the production of cyto
kines (gamma-interferon (IFN-gamma), interleukin-4 (IL-4), IL-6 and IL-10)
using both unstimulated cells and cells stimulated with the T cell mitogen
phytohaemagglutinin (PHA). Serum levels of IL-10 were determined using an E
LISA method, serum levels of IL-6 were determined using a bioassay and anti
-dr DNA antibodies were analysed by immunofluorescence.
Results
The SLE patient group had significantly increased numbers of cells spontane
ously producing IL-10 and IL-6 as compared to healthy controls (P = 0.01 an
d 0.03, respectively). The number of cells producing IL-10 and IL-6 after P
HA-stimulation was also increased in SLE patients (P = 0.01 and < 0.0004, r
espectively). Serum IL-10 and IL-6 levels were also significantly increased
in SLE patients (P < 0.0004 and 0.0005, respectively). Serum IL-10 levels
correlated with the titre of anti-ds DNA antibodies in the patients. No cor
relation was found between disease activity or clinical profiles and the pr
oduction or serum levels of cytokines except for a weak correlation (not st
atistically significant) between levels of IL-10 in the sera and disease ac
tivity as measured by the SLEDAI but not by the SLAM index.
Conclusion
Our results confirm earlier reports that. SLE patients have an increased pr
oduction as well as increased serum levels of the type 2 cytokines IL-10 an
d IL-6. We found no significant correlation between IL-6 and IL-10 and dise
ase activity or clinical profiles. Serum IL-10 levels correlated with the t
itre of anti-ds DNA antibodies in the SLE patients. In summary our result i
ndicate that the increased IL-10 production in SLE could be constitutive.