Donor specific antibody surveillance among pediatric kidney transplant programs: A report from the improving renal

Emily J Steinbach1, Gina M Barletta2, Hiren P Patel3

  • 1Division of Nephrology, Dialysis, and Transplantation, University of Iowa Stead Family Children's Hospital, Iowa City, Iowa, USA.

Insights

Pediatric kidney transplant centers vary in donor specific antibody (DSA) monitoring and management protocols. This survey highlights current practices and provides a reference for de novo (dn) DSA surveillance in children.

Area of Science:

  • Pediatric Nephrology
  • Transplant Immunology
  • Organ Transplantation

Background:

  • Kidney transplantation (KT) is the primary treatment for pediatric end-stage kidney disease.
  • Advances in immunosuppression and donor specific antibody (DSA) testing improve allograft survival.
  • However, significant variability exists in DSA surveillance and de novo (dn) DSA management among pediatric KT programs.

Purpose of the Study:

  • To survey pediatric transplant nephrologists regarding their practices for DSA surveillance and dnDSA management.
  • To identify current trends and variations in monitoring and treatment strategies.
  • To establish a reference for pediatric dnDSA monitoring.

Main Methods:

  • A voluntary, web-based survey was conducted among pediatric transplant nephrologists in the Improving Renal Outcomes Collaborative (IROC) from 2019-2020.
  • The survey collected data on the frequency and timing of routine DSA surveillance.
  • It also assessed theoretical management strategies for dnDSA in stable graft function settings.

Main Results:

  • 29 out of 30 IROC centers responded.
  • DSA screening occurs approximately every 3 months in the first year post-transplant.
  • Management decisions are primarily guided by antibody mean fluorescent intensity and trends, with elevated creatinine prompting DSA assessment.
  • Most centers (24/29) continue monitoring or intensify immunosuppression upon dnDSA detection in stable grafts.
  • 10/29 centers perform allograft biopsies for dnDSA even with stable graft function.

Conclusions:

  • This study represents the largest survey of pediatric transplant nephrologist practices concerning DSA monitoring.
  • It provides valuable insights into current surveillance and management patterns for dnDSA in pediatric kidney transplant recipients.
  • The findings serve as a benchmark for standardizing dnDSA monitoring protocols.
Abstract

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