Allograft outcomes of treated children with kidney transplant who developed plasma cell-rich acute rejection (PCAR): A single center's experience

Pediatr Transplant. 2019 Sep;23(6):e13500. doi: 10.1111/petr.13500.

Abstract

Introduction: PCAR is a rare form of ACR that may compromise renal allografts. This review evaluates the outcomes of a protocol used to treat PCAR (Study group), and compares these outcomes with a matched cohort with ACR (Control group).

Methods: A retrospective analysis of 138 of pRTRs who underwent renal allograft biopsies between January 2008 and November 2016.

Results: Seven biopsies revealed in situ hybridization of EBER-negative PCAR (5%). Three Study group pRTRs lost their grafts within 3 months after rejection (43%). None of the Control group pRTRs lost their graft during this period. At the time of rejection, eGFR was different between the Control and Study groups (27.0 ± 19.9 mL/min per m2 vs 40.0 ± 10.6 mL/min/1.73 m2 , respectively; P < 0.05). Among Study group pRTRs with functioning allografts (n = 4), treatment resulted in an increase in eGFR from nadir levels (27.0 ± 19.9 vs 55.6 ± 18.3 mL/min/1.73 m2 , P < 0.05). In the Study group, complications included neutropenia, BK and EBV viremia, and infusion-related hypotension and hypertension.

Summary: (a) Graft loss in Study group while remaining high (43%) was lower than that reported in the published pediatric literature. (b) Our protocol was associated with improvement in eGFR in all surviving pRTRs within the Study group. (c) No life-threatening complications or malignancy were reported during the observation period.

Keywords: pediatric renal transplant recipients; plasma cell rich acute rejection.

MeSH terms

  • Adolescent
  • Allografts
  • B-Lymphocytes / cytology
  • Biopsy
  • Child
  • Female
  • Follow-Up Studies
  • Glomerular Filtration Rate
  • Graft Rejection / immunology*
  • Graft Survival*
  • Humans
  • Hypotension
  • Immunosuppressive Agents / therapeutic use
  • Kidney Transplantation*
  • Male
  • Plasma Cells / cytology*
  • Retrospective Studies
  • Transplantation, Homologous
  • Treatment Outcome

Substances

  • Immunosuppressive Agents