Acceptable mismatching at the class II epitope level: the Canadian experience

Curr Opin Organ Transplant. 2014 Aug;19(4):442-6. doi: 10.1097/MOT.0000000000000104.

Abstract

Purpose of review: To summarize the evidence concerning human leukocyte antigen (HLA) epitope mismatch analysis as a means to predict donor-specific antibody (DSA) development and allograft survival.

Recent findings: HLA epitope mismatch analysis outperforms traditional whole molecule antigen mismatch for predicting the risk of de-novo DSA development. By analyzing the number of epitope mismatches for a given donor-recipient pair, thresholds have been identified to stratify patients into those at high or low risk of de-novo DSA development. Epitope specificity assignment in patients who develop de-novo DSA compared with controls who do not provides an opportunity to study the relative immunogenicity of mismatched HLA epitopes.

Summary: Recognizing that de-novo DSA is a major cause of graft loss, HLA epitope mismatch analysis is a strategy to minimize de-novo DSA development and improve long-term graft survival.

Publication types

  • Review

MeSH terms

  • Antibodies / immunology
  • Canada
  • Epitopes / immunology*
  • Graft Survival / immunology
  • Histocompatibility Antigens Class II / immunology*
  • Histocompatibility Testing
  • Humans
  • Transplantation, Homologous

Substances

  • Antibodies
  • Epitopes
  • Histocompatibility Antigens Class II