Synovial fluid levels of complement SC5b-9 and fragment Bb are elevated in patients with rheumatoid arthritis

Authors

  • James P. Brodeur MD,

    1. Division of Rheumatology, Allergy and Immunology, the Department of Internal Medicine, Medical College of Virginia, Virginia Commonwealth University, Richmond
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  • Shaun Ruddy MD,

    1. Division of Rheumatology, Allergy and Immunology, the Department of Internal Medicine, Medical College of Virginia, Virginia Commonwealth University, Richmond
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  • Lawrence B. Schwartz MD, PhD,

    1. Division of Rheumatology, Allergy and Immunology, the Department of Internal Medicine, Medical College of Virginia, Virginia Commonwealth University, Richmond
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  • George Moxley MD

    Corresponding author
    1. Division of Rheumatology, Allergy and Immunology, the Department of Internal Medicine, Medical College of Virginia, Virginia Commonwealth University, Richmond
    • Division of Rheumatology, Allergy and Immunology, Medical College of Virginia, Box 263, MCV Station, Richmond, VA 23298-0263
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Abstract

To determine whether complement turnover in synovial fluids of patients with rheumatoid arthritis (RA) reflects activation by the classical or alternative pathway, we used novel immunoassays to measure products of complement activation (the membrane attack complex SC5b-9 and the cleavage fragments Bb and C4d). Mean synovial fluid levels of SC5b-9 were more than 8 times higher in RA than in crystal-induced arthritis (gout and pseudogout) and over 16 times higher than in degenerative joint disease (DJD). Similarly, Bb levels were more than 3 times higher in RA synovial fluids than in crystal-induced arthritis and over 7 times higher than in DJD. Levels of C4d did not differ among the groups. SC5b-9 levels correlated with synovial fluid C3 anaphylatoxin (C3a), Bb, and C4d levels (r = 0.81, 0.62, and 0.51, respectively). In patients with RA, synovial fluid SC5b-9 levels correlated with C3a and Bb (r = 0.6 and 0.56, respectively) but not with C4d. Therefore, novel assays for complement activation indicate that both classical and alternative pathways are involved in complement turnover and that the alternative pathway contributes more to complement activation in RA than in DJD or crystal-induced arthritis.

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