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Metabolism of c4 and factor b in rheumatoid arthritis

✍ Scribed by Roy A. Kaplan; John G. Curd; David H. Deheer; Dennis A. Carson; Michael K. Pangburn; HANS J. Müller-E Berhard; John H. Vaughan


Publisher
John Wiley and Sons
Year
1980
Tongue
English
Weight
829 KB
Volume
23
Category
Article
ISSN
0004-3591

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✦ Synopsis


Abstract

Metabolic turnover determined by radioiodide labeled C4 and Factor B was studied in 18 patients with rheumatoid arthritis (RA) and 19 normal control subjects as a means of estimating the relative ratio of consumption of components in the classical and alternative pathways of complement activation. Predominance of fractional catabolic rate (FCR) of C4 over Factor B was demonstrated with differentially labeled C4 and Factor B. The hypercatabolism occurred in the extravascular space. C4 FCR correlated significantly with rheumatoid factor (RF) determined in a hemolytic assay (r~s~ = 0.72), measured as IgG RF (r~s~ = 0.57), and as IgM RF (r~s~ = 0.45). There were no significant correlations with several other antibodies measured. These results are consistent with the hypothesis that RA is a systemic, extravascular immune complex disease, in which RF immune complexes play a significant pathogenetic role principally via activation of the classical pathway of complement.


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