Complement deposition in glomerular diseases.

G B di Belgiojoso; A Tarantino; A Durante; L Guerra

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PubMed · 1105561

Complement deposition in glomerular diseases.

G B di Belgiojoso·A Tarantino·A Durante·L Guerra

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Abstract

Biopsies from 400 patients affected by glomerular diseases, both "primary" and secondary to systemic diseases, have been studied by immunofluorescence. Staining was performed for immunoglobulins fibrogen and C1q, C4, C3 and C3A. C1q, C4 and C3 were positive in a high percentage of cases in focal glomerulosclerosis, membranoproliferative glomerulonephritis, lupus nephritis and essential cryoglobulinaemia glomerulonephritis. C1q and C4 were very rarely present in focal proliferative glomerulonephritis and rheumatoid purpura glomerulonephritis. C3A was found frequently only in acute glomerulonephritis. Results are discussed with reference to their diagnostic value and to information about mechanisms of complement activation.

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Complement C1 Complement C3 Complement C4 Complement System Proteins Fluorescent Antibody Technique Glomerulonephritis Humans Kidney Diseases Kidney Glomerulus Sclerosis Comparative Study Journal Article

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G B di Belgiojoso, A Tarantino, A Durante, L Guerra. 1975. Complement deposition in glomerular diseases.. https://pubmed.ncbi.nlm.nih.gov/1105561/

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