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Kidney transplantation in children and adolescents with C3 glomerulopathy or immune complex membranoproliferative glomerulonephritis: a real-world study within the CERTAIN research network

  • Christian Patry
  • , Nicholas J.A. Webb
  • , Manuel Feißt
  • , Kai Krupka
  • , Jan Becker
  • , Martin Bald
  • , Benedetta Antoniello
  • , Ilmay Bilge
  • , Bora Gulhan
  • , Julien Hogan
  • , Nele Kanzelmeyer
  • , Ozan Ozkaya
  • , Anja Büscher
  • , Anne Laure Sellier-Leclerc
  • , Mohan Shenoy
  • , Lutz T. Weber
  • , Alexander Fichtner
  • , Britta Höcker
  • , Matthias Meier
  • , Burkhard Tönshoff
  • Heidelberg University 
  • Novartis
  • University of Cologne
  • Klinikum Stuttgart
  • Azienda Ospedaliera di Padova
  • Koc University
  • Robert-Debré Children University Hospital-APHP
  • Hannover Medical School
  • Istinye University
  • University of Duisburg-Essen
  • Hospices civils de Lyon
  • Manchester University NHS Foundation Trust

Research output: Contribution to journalArticlepeer-review

5 Citations (Scopus)

Abstract

Background: Complement 3 glomerulopathy (C3G) and immune complex membranoproliferative glomerulonephritis (IC-MPGN) are ultra-rare chronic kidney diseases with an overall poor prognosis, with approximately 40–50% of patients progressing to kidney failure within 10 years of diagnosis. C3G is characterized by a high rate of disease recurrence in the transplanted kidney. However, there is a lack of published data on clinical outcomes in the pediatric population following transplantation. Methods: In this multicenter longitudinal cohort study of the Cooperative European Paediatric Renal Transplant Initiative (CERTAIN) registry, we compared the post-transplant outcomes of pediatric patients with C3G (n = 17) or IC-MPGN (n = 3) with a matched case–control group (n = 20). Results: Eleven of 20 children (55%) with C3G or IC-MPGN experienced a recurrence within 5 years post-transplant. Patients with C3G or IC-MPGN had a 5-year graft survival of 61.4%, which was significantly (P = 0.029) lower than the 5-year graft survival of 90% in controls; five patients with C3G or IC-MPGN lost their graft due to recurrence during this observation period. Both the 1-year (20%) and the 5-year (42%) rates of biopsy-proven acute rejection episodes were comparable between patients and controls. Complement-targeted therapy with eculizumab, either as prophylaxis or treatment, did not appear to be effective. Conclusions: These data in pediatric patients with C3G or IC-MPGN show a high risk of post-transplant disease recurrence (55%) and a significantly lower 5-year graft survival compared to matched controls with other primary kidney diseases. These data underscore the need for post-transplant patients for effective and specific therapies that target the underlying disease mechanism. Graphical abstract: (Figure presented.)

Original languageEnglish
Pages (from-to)3569-3580
Number of pages12
JournalPediatric Nephrology
Volume39
Issue number12
DOIs
Publication statusPublished - Dec 2024

Keywords

  • Complement 3 glomerulopathy
  • Graft survival
  • Immune complex membranoproliferative glomerulonephritis
  • Pediatric kidney transplantation
  • Recurrence

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