H. Mangge et al., Long-term follow-up of cytokines and soluble cytokine receptors in peripheral blood of patients with juvenile rheumatoid arthritis, J INTERF CY, 19(9), 1999, pp. 1005-1010
Plasma levels of interleukin-1 beta (IL-1 beta), IL-2, soluble IL-2 recepto
r (sIL-2R), IL-6, IL-8, tumor necrosis factor-alpha (TNF-alpha), and the p6
0 soluble TNF receptor (sTNFR) were repeatedly determined by enzyme-linked
immunosorbent assays (ELISA) in 35 patients with different subtypes of juve
nile rheumatoid arthritis (JRA) during an observation period of up to 36 mo
nths. The data were related to conventional inflammatory parameters and dis
ease activity. Patients with systemic disease showed the most pronounced el
evations of plasma cytokines, followed by polyarticular and pauciarticular
JRA. Soluble receptors sIL-2R and sTNFR were consistently elevated in patie
nts of all JRA subtypes and indicated disease activity even in patients wit
h normal C-reactive protein (CRP). In contrast, the determination of IL-1 b
eta, IL-2, IL-8, and TNF-alpha revealed strikingly different individual pro
files in patients of the same clinical subtype of JRA and irrespective of d
isease activity. It is concluded that the determination of sIL-2R and sTNFR
may be relevant for monitoring JRA, as they indicate disease activity also
in cases with unaltered conventional inflammatory parameters. The differen
t individual cytokine profiles of patients within identical subtypes of dis
ease suggest JRA to be even more heterogeneous than hitherto assumed. The d
ata should be considered in attempts to develop anticytokine strategies in
the therapy of JRA.