Coexistence of different circulating anti-podocyte antibodies in membranous nephropathy

Autor: Corrado Murtas, Pietro Ravani, Francesca Bruno, Maurizio Bruschi, Piergiorgio Messa, Riccardo Magistroni, Francesco Scolari, Giovanni Candiano, Landino Allegri, Andrea Magnano, Fernando C. Fervenza, Maria Luisa Carnevali, Gian Marco Ghiggeri, Lucia Argentiero, L. Furci, Renato Alberto Sinico, Antonella Radice, Gabriella Moroni, Loreto Gesualdo
Přispěvatelé: Murtas, C, Bruschi, M, Candiano, G, Moroni, G, Magistroni, R, Magnano, A, Bruno, F, Radice, A, Furci, L, Argentiero, L, Carnevali, M, Messa, P, Scolari, F, Sinico, R, Gesualdo, L, Fervenza, F, Allegri, L, Ravani, P, Ghiggeri, G
Rok vydání: 2012
Předmět:
Male
Registrie
nefrologia
Time Factors
Epidemiology
glomerulonefrite membranosa
Critical Care and Intensive Care Medicine
Glomerulonephritis
Membranous

Immunoglobulin G
Retrospective Studie
Medicine
Registries
antigene
Proteinuria
biology
Podocytes
Glomerulosclerosis
Focal Segmental

Middle Aged
Glomerulonephritis
Membranou

Isotype
Autoantibodie
sindrome nefrosica
Italy
Nephrology
Linear Model
Female
Neprilysin
medicine.symptom
Human
Adult
Adolescent
Logistic Model
Time Factor
Podocyte
Nephropathy
Young Adult
Antigen
Membranous nephropathy
Aldehyde Reductase
Humans
Autoantibodies
Retrospective Studies
Aged
Transplantation
business.industry
Superoxide Dismutase
Receptors
Phospholipase A2

Autoantibody
Glomerulonephritis
IGA

Original Articles
medicine.disease
Logistic Models
Phosphopyruvate Hydratase
Immunology
Linear Models
biology.protein
business
Popis: Summary Background and objectives The discovery of different podocyte autoantibodies in membranous nephropathy (MN) raises questions about their pathogenetic and clinical meaning. This study sought to define antibody isotypes and correlations; to compare levels in MN, other glomerulonephritides, and controls; and to determine their association with clinical outcomes. Design, setting, participants, & measurements Serum IgG1 ,I gG3 ,a nd IgG4 against aldose reductase (AR), SOD2, and a-enolase (aENO) were measured at diagnosis in 186 consecutive MN patients, in 96 proteinuric controls (36 with FSGS, and 60 with IgA nephropathy), and in 92 healthy people recruited in four Italian nephrology units. Anti-phospholipase A2 receptor (PLA2r) and anti-neutral endopeptidase (NEP) IgG4 were titrated in the same specimens. Association with 1-year follow-up clinical parameters was studied in 120 patients. Results IgG4 was the most common isotype for all antibodies; IgG1 and IgG3 were nearly negligible. IgG4 levels werepositiveinasignificantproportionofMNpatients(AR,34%;SOD2,28%;aENO,43%).Antibodytiterswere higher in MN than in healthy and pathologic controls (P,0.005). Anti-NEP IgG4 did not differ from normal controls (P=0.12). Anti-PLA2r IgG4 was detected in 60% of patients and correlated with anti-AR, anti-SOD2, and anti-aENO IgG4 (P,0.001). In MN patients negative for the whole antibody panel (20%), 1-year proteinuria was lower compared with patients with at least one antibody positivity (P,0.05). Conclusions Our data suggest that IgG4 is the prevalent isotype for antibodies against cytoplasmic antigens of podocytes (AR, SOD2, aENO). Their levels were higher than in other proteinuric glomerulonephritides and in normal controls and were correlated with anti-PLA2r. Only baseline negativity for all known antibodies predicted lower 1-year proteinuria. Clin J Am Soc Nephrol 7: ccc–ccc, 2012. doi: 10.2215/CJN.02170312
Databáze: OpenAIRE