EXPRESSION OF IL-2R, IL-4R, IL-6R ON PERIPHERAL-BLOOD LYMPHOCYTES IN SYSTEMIC LUPUS-ERYTHEMATOSUS AND CORRELATION WITH DISEASE-ACTIVITY - APROSPECTIVE-STUDY
Eyt. Chan et al., EXPRESSION OF IL-2R, IL-4R, IL-6R ON PERIPHERAL-BLOOD LYMPHOCYTES IN SYSTEMIC LUPUS-ERYTHEMATOSUS AND CORRELATION WITH DISEASE-ACTIVITY - APROSPECTIVE-STUDY, Journal of Clinical Pathology, 49(8), 1996, pp. 660-663
Aims-To study the expression of interleukin-2 receptor (IL-2R), interl
eukin-4 receptor (IL-4R) and interleukin-6 receptor (IL-6R) on periphe
ral blood lymphocytes (PBL) in patients with systemic lupus erythemato
sus (SLE); to correlate the level of expression of these receptors wit
h SLE disease activity. Methods-Peripheral blood lymphocytes were stud
ied by a high sensitivity flow cytometry technique using monoclonal an
tibodies directed against CD25 (IL-2R alpha chain), CD122 (IL-2R beta
chain), CD124 (IL-4R), and CD126 (IL-6R). SLE disease activity was sco
red using the SLE Disease Activity Index, C3 and C3, concentrations, a
nti-dsDNA level, and absolute lymphocyte count. Results-Compared with
normal controls, PBL from. patients with SLE had a higher percentage o
f CD25+ cells (median 20.8% v 16.5%) and a lower percentage of CD122cells (median 13.1% v 22.4%). The difference in CD122+ cells was great
er in the CD122(weak) population than the CD122(strong) (natural kille
r cell) population. The percentages of CD124+ and CD126+ PBLs in patie
nts with SLE and controls were similar. On CD25+ cells, the relative a
ntigenic level of the IL-2R alpha chain was significantly higher in pa
tients with SLE (median 2.01 v 1.81). The relative antigenic levels of
CD122+, CD124+ and CD126+ cells were similar in patients and controls
. Neither the percentages nor the relative antigenic levels of all of
these cytokine receptors were correlated with any of the parameters of
disease activity. Conclusion-Lymphocyte activation in patients with S
LE was evident from the increase in CD25 expression on PBL, with a rec
iprocal decrease in CD122 expression. As tile expression of IL-2R, IL-
4R, IL-6R did not correlate with disease activity, it seems that these
cytokine/receptor systems do not play a direct role in disease activa
tion in SLE.