Rheumatology 2000; 39: 432-438
© 2000 British Society for Rheumatology
Tumour necrosis factor alpha and its soluble receptors in juvenile chronic arthritis
Centre for Paediatric and Adolescent Rheumatology, UCL, London, UK and
1 Division of Immunology and Allergy, University Hospital, Geneva, Switzerland
Objective. To identify possible imbalance of tumour necrosis factor alpha (TNF
) and its soluble receptors in the different subgroups of juvenile chronic arthritis (JCA).
Methods. Serum and synovial fluid samples from 45 children were examined, 25 pauciarticular JCA, 13 polyarticular JCA and seven spondyloarthropathy. TNF
, sTNFRI and sTNFRII levels were measured by EASIA and enzyme-linked immunosorbent assay (ELISA). Analysis of the results was carried out using non-parametric tests: KruskalWallis one-way analysis of variance was used to compare the three clinical subgroups; the MannWhitney U-test was used to compare group medians.
Results. Thirty-three serum samples were assayed for TNF
. There was no significant difference between the three groups using the KruskalWallis analysis of variance. Analysis of synovial fluid TNF levels showed significantly lower levels in the spondyloarthropathy group compared with the pauciarticular JCA (P = 0.01) and the polyarticular group (P = 0.002). Significantly higher levels of sTNFRI were observed in the synovial fluid of the polyarticular JCA group compared with the pauciarticular JCA group (P = 0.004) and similarly for sTNFRII (P = 0.03). Molar ratios were calculated for TNF vs sTNFRI. The sTNFRI/TNF
ratio was significantly higher in the spondyloarthropathy group compared with the pauci- (P 0.003) and the polyarticular JCA subgroups (P = 0.003). The combined soluble receptor levels expressed as molar ratio to TNF again showed a significantly higher ratio in the spondyloarthropathy group compared with the pauciarticular group (P = 0.01) and compared with the polyarticular group (P = 0.05).
Conclusion. These results suggest that the increased joint destruction observed in polyarticular disease compared with the other two subtypes may be related to the lower sTNFR/TNF
ratios observed.
KEY WORDS: Juvenile chronic arthritis, Synovial fluid, Cytokines, Tumour necrosis factor alpha, Soluble TNF receptors.
Correspondence to: P. Woo, Centre for Paediatric and Adolescent Rheumatology, UCL, Department of Molecular Pathology, The Windeyer Institute of Medical Sciences, 46 Cleveland Street, London, W1P 6DB, UK.
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