1963
DOI: 10.3109/rhe1.1963.9.issue-1-4.21
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Studies on the Depressed Hemolytic Complement Activity of Synovial Fluid in Adult Rheumatoid Arthritis

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Cited by 59 publications
(9 citation statements)
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“…Elution of rheumatoid synovium using acid pH or high ionic-strength buffers has yielded predominantly IgG and albumin and C3 (21,22), and complexes rich in IgG and containing IgG and IgM rheumatoid factors have been identified. Striking diminution in CH50 (23)(24)(25) and C2 (26) has been recorded by both single radial diffusion and stoichiometric hemolytic titrations (27,28). Further evidence for the activation of late components including a reduction of C9 in seropositive patients has been noted more recently (29).…”
Section: Discussionmentioning
confidence: 92%
“…Elution of rheumatoid synovium using acid pH or high ionic-strength buffers has yielded predominantly IgG and albumin and C3 (21,22), and complexes rich in IgG and containing IgG and IgM rheumatoid factors have been identified. Striking diminution in CH50 (23)(24)(25) and C2 (26) has been recorded by both single radial diffusion and stoichiometric hemolytic titrations (27,28). Further evidence for the activation of late components including a reduction of C9 in seropositive patients has been noted more recently (29).…”
Section: Discussionmentioning
confidence: 92%
“…The first studies of synovial fluid complement activity in disease observed that to make meaningful comparisons, it was necessary to make a correction for total synovial fluid protein (1,2). Thus it was described that corrected complement activity in synovial fluids of patients with rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE) were lower than predicted by total protein (1,2).…”
mentioning
confidence: 99%
“…Corrected complement levels in fluids from patients with gout and Reiter's disease are said to be the same or greater than those of DJD (1)(2)(3)5,9,11,13,14). Any sizable overlap of ranges diminishes the usefulness of complement determinations for diagnosis or for identification of new syndromes in which complement activation plays a pathogenetic role.…”
mentioning
confidence: 99%
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“…Chronic inflammation is a characteristic feature of the chronic arthritis diseases, and there is now convincing evidence that the complement system is activated in both seropositive (Hedberg, 1963(Hedberg, , 1964(Hedberg, , 1967Pekin & Zvaifler, 1964;Fostiropoulis, Austen & Bloch, 1965;Barnett, Bienenstock & Bloch, 1966;Peltier, Coste & Delbarre, 1966; Vaughan, Barnett, Sobel & Jacox, 1968;Zvaifler, 1969; Ruddy & Austen, 1970;Hedberg, Lundh & Laurell, 1970;Gligore, Bolishu, Duter & Podut, 1971; Ruddy, Everson, Schur & Austen, 1971; Ruddy, Muller-Eberhard & Austen, 1971; Britton & Schur, 1971; Ward & Zvaifler, 1971;Versey, Hobbs & Holt, 1973;and seronegative (Whaley, Canesi, Moseley, Morrow, Sturrock, Mitchell & Dick, 1974) arthritides. As there is at present no cure for these disorders, treatment is simply symptomatic.…”
Section: Introductionmentioning
confidence: 99%