Incidence and outcomes of BK virus allograft nephropathy among ABO- and HLA-incompatible kidney transplant recipients

Clin J Am Soc Nephrol. 2012 Aug;7(8):1320-7. doi: 10.2215/CJN.00770112. Epub 2012 May 24.

Abstract

Background and objectives: ABO-incompatible kidney transplant recipients may have a higher incidence of BK virus allograft nephropathy (BKVAN) compared with ABO-compatible recipients. It is unclear whether HLA-incompatible recipients share this risk or whether this phenomenon is unique to ABO-incompatible recipients. DESIGN, SETTING, PARTICIPATION, MEASUREMENTS: This study analyzed adult incompatible kidney transplant recipients from 1998 to 2010 (62 ABO-incompatible and 221 HLA-incompatible) and identified patients in whom BKVAN was diagnosed by biopsy (per protocol or for cause). This was a retrospective analysis of a prospectively maintained database that compared BKVAN incidence and outcomes between ABO- and HLA-incompatible recipients, respectively. BKVAN link to rejection and graft accommodation phenotype were also explored. The Johns Hopkins Institutional Review Board approved this study.

Results: Risk for BKVAN was greater among ABO-incompatible than HLA-incompatible patients (17.7% versus 5.9%; P=0.008). Of BKVAN cases, 42% were subclinical, diagnosed by protocol biopsy. ABO-incompatibility and age were independent predictors for BKVAN on logistic regression. C4d deposition without histologic features of glomerulitis and capillaritis (graft accommodation-like phenotype) on 1-year biopsies of ABO-incompatible patients with and without BKVAN was 40% and 75.8%, respectively (P=0.04). Death-censored graft survival (91%) and serum creatinine level among surviving kidneys (1.8 mg/dl) were identical in ABO- and HLA-incompatible patients with BKVAN (median, 1399 and 1017 days after transplantation, respectively).

Conclusions: ABO-incompatible kidney recipients are at greater risk for BKVAN than HLA-incompatible kidney recipients. ABO-incompatible recipients not showing the typical graft accommodation-like phenotype may be at heightened risk for BKVAN, but this observation requires replication among other groups.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • ABO Blood-Group System / immunology*
  • Adolescent
  • Adult
  • Aged
  • BK Virus / pathogenicity*
  • Baltimore / epidemiology
  • Biomarkers / blood
  • Biopsy
  • Blood Group Incompatibility / immunology*
  • Chi-Square Distribution
  • Complement C4b / analysis
  • Creatinine / blood
  • Female
  • Graft Rejection / epidemiology
  • Graft Rejection / immunology
  • Graft Rejection / virology
  • Graft Survival
  • HLA Antigens / immunology*
  • Histocompatibility*
  • Humans
  • Incidence
  • Kidney Transplantation / adverse effects
  • Kidney Transplantation / immunology*
  • Logistic Models
  • Male
  • Middle Aged
  • Multivariate Analysis
  • Odds Ratio
  • Peptide Fragments / analysis
  • Polyomavirus Infections / diagnosis
  • Polyomavirus Infections / epidemiology
  • Polyomavirus Infections / virology*
  • Retrospective Studies
  • Risk Assessment
  • Risk Factors
  • Time Factors
  • Treatment Outcome
  • Tumor Virus Infections / diagnosis
  • Tumor Virus Infections / epidemiology
  • Tumor Virus Infections / virology*
  • Young Adult

Substances

  • ABO Blood-Group System
  • Biomarkers
  • HLA Antigens
  • Peptide Fragments
  • Complement C4b
  • complement C4d
  • Creatinine