作者: W G Couser , P J Baker , M Schulze , C J Pruchno , M Burns
DOI:
关键词: Complement system 、 Glomerular deposits 、 Membranous nephropathy 、 Complement factor I 、 Immune complex disease 、 Heymann Nephritis 、 Complement C3c 、 Glomerulonephritis 、 Immunology 、 Biology
摘要: In antibody-mediated glomerular disease, deposits of C3 (C3b) are common and degraded by factor I to C3c C3d. However, the kinetics C3b degradation in glomerulonephritis have not been defined. To do this, we studied three models complement-dependent with established (passive Heymann nephritis, cationized immunoglobulin G membranous nephropathy, concanavalin A-anticoncanavalin A glomerulonephritis). deposition was halted administration cobra venom factor, disappearance C3d from glomeruli measured specific antibodies quantitative fluorescence densitometry. Results showed that were reduced over 85% within 24 hours all models. clearance unaffected site or mechanism deposit formation. persisted despite lack ongoing complement activation. passive nephritis when disease activity monitored urinary C5b-9 excretion, cleared parallel return urine excretion normal values. We conclude cessation Positive staining for utilizing antibody portion documents recent activation usually reflecting new immune