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Functional Characterization of Anti-C3bBb Autoantibodies and C3 Glomerulopathy Phenotype.
Roquigny, Julia; Meuleman, Marie-Sophie; El Sissy, Carine; Cailliez, Mathilde; Servais, Aude; Roussey, Gwenaelle; Baudouin, Véronique; Decramer, Stéphane; Nobili, François; Wynckel, Alain; Sellier Leclerc, Anne-Laure; Lapeyraque, Anne-Laure; Martins, Paula Vieira; Meri, Seppo; Dragon-Durey, Marie-Agnès; Chauvet, Sophie; Frémeaux-Bacchi, Véronique.
Afiliação
  • Roquigny J; Inflammation, Complement and Cancer Team, Cordeliers Research Center, Institut National de la Santé et de la Recherche Médicale (INSERM) Unité Mixte de Recherche (UMR) S1138, Paris, France.
  • Meuleman MS; Department of Bacteriology and Immunology, University of Helsinki, Finland.
  • El Sissy C; Inflammation, Complement and Cancer Team, Cordeliers Research Center, Institut National de la Santé et de la Recherche Médicale (INSERM) Unité Mixte de Recherche (UMR) S1138, Paris, France.
  • Cailliez M; Inflammation, Complement and Cancer Team, Cordeliers Research Center, Institut National de la Santé et de la Recherche Médicale (INSERM) Unité Mixte de Recherche (UMR) S1138, Paris, France.
  • Servais A; Department of Immunology, Assistance Publique- Hôpitaux de Paris (AP-HP), Georges Pompidou European Hospital, Paris, France.
  • Roussey G; Department of Pediatric Nephrology, Marseille University Hospital, France.
  • Baudouin V; Department of Nephrology, Necker Hospital, Paris, France.
  • Decramer S; Department of Pediatric Nephrology, Nantes University Hospital, France.
  • Nobili F; Department of Pediatric Nephrology, Robert Debre Hospital, Paris, France.
  • Wynckel A; Department of Nephrology, Toulouse University Hospital, France.
  • Sellier Leclerc AL; Department of Nephrology, Besancon University Hospital, France.
  • Lapeyraque AL; Department of Nephrology, Reims University Hospital, France.
  • Martins PV; Department of Pediatric Nephrology, Rhumatology, Dermatology, Lyon University Hospital, France.
  • Meri S; Department of Pediatry, Saint Justine University Hospital, Montreal, Canada.
  • Dragon-Durey MA; Department of Immunology, Assistance Publique- Hôpitaux de Paris (AP-HP), Georges Pompidou European Hospital, Paris, France.
  • Chauvet S; Department of Bacteriology and Immunology, University of Helsinki, Finland.
  • Frémeaux-Bacchi V; Inflammation, Complement and Cancer Team, Cordeliers Research Center, Institut National de la Santé et de la Recherche Médicale (INSERM) Unité Mixte de Recherche (UMR) S1138, Paris, France.
J Am Soc Nephrol ; 2024 Sep 26.
Article em En | MEDLINE | ID: mdl-39325562
ABSTRACT

BACKGROUND:

C3 nephritic factors, i.e. autoantibodies that stabilize the C3 convertase of the alternative pathway are the most frequent acquired abnormality in C3 glomerulopathy and primary immunoglobulin-mediated membranoproliferative GN (Ig-MPGN).

METHODS:

Our study included 27 patients with C3 glomerulopathy (n=21) or Ig-MPGN (n=6), of whom 78% were children at disease onset. At the time of sampling, 13/19 (68%) patients with low C3 levels and 8/8 (100%) patients with normal C3 levels were positive for C3 nephritic factors by haemolytic assay. Using novel Luminex assays, we performed a screening for IgG that recognize and affect the formation and/or the stabilization of the alternative pathway C3 convertase (C3bBb).

RESULTS:

Using Luminex assays, an increase in C3bBb formation and/or stabilization was observed in the presence of IgG from 18/27 patients, including 9 with a double-function, 6 only enhancing the C3bBb formation, and 3 that exclusively stabilized C3bBb. All patients presenting a formation and stabilization function had a low C3 level, versus 55% without this double-function. The level of C3bBb formation correlated to the plasmatic C3 but not sC5b-9 levels. The stabilization of C3bBb did not correlate with C3 or sC5b-9 levels. At the last follow-up, 5/27 patients (19%) reached kidney failure after a median delay of 87 [52,119] months. The patients positive for double-function anti-C3bBb antibodies had a 5-year kidney survival of 70% compared to 100% in those negative (P=0.02).

CONCLUSIONS:

Our findings highlight the association of the dual function of C3bBb formation and stabilization with severe C3 consumption and poor kidney survival in C3 glomerulopathy and Ig-MPGN.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Am Soc Nephrol Assunto da revista: NEFROLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Am Soc Nephrol Assunto da revista: NEFROLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: França