Acute Rejection Clinically Defined Phenotypes Correlate With Long-term Renal Allograft Survival

Transplantation. 2015 Oct;99(10):2167-73. doi: 10.1097/TP.0000000000000706.

Abstract

Background: Classification of acute rejection (AR) based on etiology and timing may provide a means for enhancing therapeutic results and allograft survival. This study evaluated graft and patient survival after the first AR episodes among kidney transplant recipients with an early or late antibody-mediated rejection (AMR), acute cellular rejection (ACR) or mixed AR (MAR).

Methods: A prospective institutional review board-approved database was queried to identify biopsy-proven first AR episodes occurring from January 2005 to October 2012. The ACR was defined by Banff criteria; borderline AR was excluded. The AMR was defined as 3 of 4 criteria: renal dysfunction, donor specific antibody, C4d positivity on biopsy, and histological changes. The MAR met criteria for both ACR and AMR. Early AR occurred within six months post-transplant. AR episodes were then assigned to 1 of the 6 categories--early AMR, early ACR, early MAR, late AMR, late ACR, and late MAR.

Results: One hundred eighty-two kidney transplant recipients identified with a first AR episode. Mean follow-up was 773 days (± 715 days). No difference was observed in patient survival. Death-censored graft survival was 84%. Death-censored graft loss was higher with late versus early AMR (P = 0.01) and late versus early ACR (P = 0.03), but not late versus early MAR (P = 0.3).

Conclusions: The AR type demonstrated a hierarchy for graft survival with ACR better than MAR better than AMR, which persisted for both early and late AR. Improvement in long-term results of AR may require development of specific treatment for individual AR types.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Biopsy
  • Complement C4b / chemistry
  • Databases, Factual
  • Female
  • Follow-Up Studies
  • Glomerular Filtration Rate
  • Graft Rejection
  • Graft Survival*
  • Humans
  • Kidney Transplantation*
  • Living Donors
  • Male
  • Middle Aged
  • Peptide Fragments / chemistry
  • Phenotype
  • Prospective Studies
  • Renal Insufficiency / mortality*
  • Renal Insufficiency / surgery*
  • Treatment Outcome

Substances

  • Peptide Fragments
  • Complement C4b
  • complement C4d