
Levels of circulating tumor necrosis factor α and interleukin‐6 in patients with rheumatoid arthritis. relationship to serum levels of hyaluronan and antigenic keratan sulfate
Author(s) -
Manicourt DanielHenri,
Triki Rafak,
Fukuda Kanji,
Devogelaer JeanPierre,
Deuxchaisnes Charles Nagant De,
Thonar Eugene J.M. A.
Publication year - 1993
Publication title -
arthritis & rheumatism
Language(s) - English
Resource type - Journals
eISSN - 1529-0131
pISSN - 0004-3591
DOI - 10.1002/art.1780360409
Subject(s) - erythrocyte sedimentation rate , rheumatoid arthritis , medicine , immunology , tumor necrosis factor alpha , endocrinology , population , arthritis , antigen , environmental health
Objective. To measure serum levels of tumor necrosis factor α (TNF α) and interleukin‐6 (IL‐6) in patients with rheumatoid arthritis (RA) and age‐matched control subjects and to study how these correlate with serum levels of hyaluronan (HA) and antigenic keratan sulfate (KS) and other biochemical as well as clinical indicators of disease activity. Methods. Immunoassays were used to measure levels of TNFα, IL‐6, HA, and antigenic KS in the serum of 35 patients with RA and a group of age‐ and sex‐matched control subjects. Clinical disease activity in the RA group was assessed using the Lansbury index. Drug intake was recorded and the erythrocyte sedimentation rate, and levels of fibrinogen, creatinine, bilirubin, alkaline phosphatase, lactate dehydrogenase, and aminotransferase were measured. Results. Serum levels of TNFα, IL‐6, and HA were significantly higher in the RA population than in the control group. In patients with RA, serum levels of HA correlated positively with serum levels of TNFα and with clinical joint scores, but only weakly with other laboratory parameters of inflammation. Serum levels of antigenic KS correlated negatively with levels of circulating TNFα, but much more weakly with other clinical and biochemical parameters of disease activity. Conclusion. These in vivo data support in vitro studies which have shown that TNFα is a potent stimulator of HA synthesis by synovial lining cells. The results strengthen the contention that serum HA may be a unique marker of synovial involvement and inflammation, rather than of only inflammation, in RA.