Increased Levels of Interleukin 33 in Sera and Synovial Fluid from Patients with Active Rheumatoid Arthritis

• Published in: Journal of rheumatology 2010-01, Vol.37 (1), p.18-25
• Main Authors: MATSUYAMA, Yasushi, OKAZAKI, Hitoaki, TOMINAGA, Shin-Ichi, MINOTA, Seiji, TAMEMOTO, Hiroyuki, KIMURA, Hirotaka, KAMATA, Yasuyuki, NAGATANI, Katsuya, NAGASHIMA, Takao, HAYAKAWA, Morisada, IWAMOTO, Masahiro, YOSHIO, Taku
• Format: Article
• Language: English
• Subjects: Adult; Aged; Aged, 80 and over; Animals; Antirheumatic Agents - therapeutic use; Arthritis, Rheumatoid - drug therapy; Arthritis, Rheumatoid - metabolism; Arthritis, Rheumatoid - pathology; Arthritis, Rheumatoid - physiopathology; Biological and medical sciences; Cells, Cultured; Diseases of the osteoarticular system; Female; Humans; Inflammatory joint diseases; Interleukin-33; Interleukins - metabolism; Joints - immunology; Joints - pathology; Leukocytes, Mononuclear - cytology; Leukocytes, Mononuclear - immunology; Male; Medical sciences; Mice; Middle Aged; Signal Transduction - physiology; Synovial Fluid - immunology
• ISSN: 0315-162X; 1499-2752
• DOI: 10.3899/jrheum.090492

Objective. To determine levels of interleukin 33 (IL-33) in serum and synovial fluid (SF) and their clinical associations in patients with rheumatoid arthritis (RA). To evaluate the ability of activated peripheral blood mononuclear cells (PBMC) and fibroblast-like synoviocytes (FLS) from RA patients to release IL-33. Methods. Sera were obtained from 59 patients with RA, 10 patients with infectious diseases, and 42 healthy volunteers. SF samples were obtained from 15 patients with RA and 13 with osteoarthritis. IL-33 levels were measured using a sandwich ELISA after removal of rheumatoid factor with protein A-Sepharose beads. FLS were stimulated with IL-1ß and tumor necrosis factor, and treated with or without chemical damage. PBMC were stimulated with anti-CD3/CD28 antibodies. The levels of IL-33 were measured in the culture supernatants and cell lysates by ELISA or immunoblotting. Results. Serum IL-33 levels were significantly higher in RA patients, especially in the high disease activity group compared to the moderate or low activity group. IL-33 levels in SF were elevated in all 15 RA patients measured. IL-33 levels were higher in SF samples than in sera in 7 RA patients measured simultaneously. The 30-kDa IL-33 precursor was detected in the culture supernatants of damaged FLS but was not detected in those of activated PBMC and non-damaged FLS. Conclusion. IL-33 levels were elevated in sera and SF samples from patients with RA, and correlated with disease activity. IL-33 was produced mainly in inflamed joints; IL-33/ST2L signaling might play an important role in joint inflammation of human RA.