Relationship Between Antibodies to Dsdna and to Soluble Cellular Antigens and Histologically Defined Glomerulonephritis in Patients with SLE

To better define the relationships between circulating autoantibodies and renal involvement in systemic lupus erythematosus (SLE), antibodies to both dsDNA and soluble cellular antigens were detected in sera from a large series of SLE patients. Significantly higher dsDNA binding activities and lower...

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Veröffentlicht in:Autoimmunity (Chur, Switzerland) Switzerland), 1990, Vol.7 (1), p.13-21
Hauptverfasser: Asero, R., Banfi, G., Radelli, L., Origgi, L., Bertetti, E., Vanoli, M., Riboldi, P.
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container_title Autoimmunity (Chur, Switzerland)
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creator Asero, R.
Banfi, G.
Radelli, L.
Origgi, L.
Bertetti, E.
Vanoli, M.
Riboldi, P.
description To better define the relationships between circulating autoantibodies and renal involvement in systemic lupus erythematosus (SLE), antibodies to both dsDNA and soluble cellular antigens were detected in sera from a large series of SLE patients. Significantly higher dsDNA binding activities and lower complement levels at onset were found in patients with renal disease; however, this was uniquely due to subjects with diffuse or focal proliferative glomerulonephritis. Patients with membranous nephropathy (MGN) showed very low dsDNA binding activities (6/9 of them being negative for dsDNA antibodies) and normal mean C3 and C4 levels. A comparison between patients with proliferative nephritis and patients without renal involvement with high dsDNA binding activities revealed significantly lower complement levels in the former group. No significant difference was observed in the prevalence of antibodies to soluble cellular antigens between patients with or without renal disease; however, nRNP antibody was two-fold more frequent in patients with MGN than in all other subgroups. This study highlights the close relationship between concurrently high anti-dsDNA and low complement levels and proliferative glomerulonephritis in SLE, and suggests that subjects with MGN may represent a subgroup of SLE patients showing peculiar serological features. Different mechanisms possibly involved in the pathogenesis of MGN in SLE are discussed.
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Significantly higher dsDNA binding activities and lower complement levels at onset were found in patients with renal disease; however, this was uniquely due to subjects with diffuse or focal proliferative glomerulonephritis. Patients with membranous nephropathy (MGN) showed very low dsDNA binding activities (6/9 of them being negative for dsDNA antibodies) and normal mean C3 and C4 levels. A comparison between patients with proliferative nephritis and patients without renal involvement with high dsDNA binding activities revealed significantly lower complement levels in the former group. No significant difference was observed in the prevalence of antibodies to soluble cellular antigens between patients with or without renal disease; however, nRNP antibody was two-fold more frequent in patients with MGN than in all other subgroups. This study highlights the close relationship between concurrently high anti-dsDNA and low complement levels and proliferative glomerulonephritis in SLE, and suggests that subjects with MGN may represent a subgroup of SLE patients showing peculiar serological features. 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ispartof Autoimmunity (Chur, Switzerland), 1990, Vol.7 (1), p.13-21
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source MEDLINE; Taylor & Francis:Master (3349 titles)
subjects Adolescent
Adult
Antibodies, Antinuclear - analysis
Antigens - immunology
Biopsy
complement
Complement C3 - analysis
Complement C4 - analysis
DNA - immunology
dsDNA antibody
Female
glomerulonephritis
Glomerulonephritis - immunology
Glomerulonephritis, Membranous - immunology
Humans
Lupus Erythematosus, Systemic - complications
Lupus Erythematosus, Systemic - immunology
Lupus Erythematosus, Systemic - pathology
Male
Middle Aged
soluble cellular antigens
Systemic lupus erythematosus
title Relationship Between Antibodies to Dsdna and to Soluble Cellular Antigens and Histologically Defined Glomerulonephritis in Patients with SLE
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