| Literature DB >> 27289077 |
Abstract
"Epitope matching" has become a buzz word in solid organ transplantation. Its goal is to improve matching between donor and recipient, to minimize risk for antibody-mediated rejection and to reduce sensitization associated with graft failure. Current software allows identification and enumeration of amino acid sequence mismatches in the form of HLA eplets; however, "eplets" and "epitopes" are not interchangeable terms, and the understanding of what contributes to the antigenicity and immunogenicity of HLA B cell epitopes is still very limited and inadequate. In fact, we still do not know what constitutes an HLA epitope or how to define it in a clinically useful way. To allow for judicious implementation of epitope matching, it is critical to explore the full spectrum of factors that affect allorecognition. In exploring antibody-binding patterns, we have uncovered a potential tool-currently hidden in plain sight-that may shed light on some aspects of epitope characteristics. © Copyright 2016 The American Society of Transplantation and the American Society of Transplant Surgeons.Entities:
Keywords: alloantibody; antibody biology; antigen presentation/recognition; histocompatibility; major histocompatibility complex (MHC); organ transplantation in general; sensitization; translational research/science
Mesh:
Substances:
Year: 2016 PMID: 27289077 DOI: 10.1111/ajt.13918
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086