| Literature DB >> 23398855 |
T H Tran1, C Unterrainer1, G Fiedler1, B Döhler1, S Scherer1, A Ruhenstroth1, M Adamek1, D Middleton2, G Opelz1.
Abstract
Natural killer (NK) cell function can be modulated by the killer cell immunoglobulin-like receptors (KIR) which interact with human leukocyte antigen (HLA) class I molecules on target cells. KIR-ligand mismatching has recently been shown by van Bergen et al. (American Journal of Transplantation 2011; 11(9): 1959-1964) to be a significant risk factor for long-term graft loss in HLA-A, -B and -DR compatible kidney transplants. To verify this potentially important finding, we performed genotyping of 608 deceased-donor kidney graft recipients and their HLA-A, -B and -DR compatible donors for KIR and HLA, using samples and clinical data provided by the Collaborative Transplant Study. Graft survival of KIR-ligand-matched and -mismatched transplants was compared. We found no impact of KIR-ligand mismatching on 10-year graft survival in HLA-A, -B, -DR compatible kidney transplants. Further analysis did not reveal a significant effect of recipient activating/inhibitory KIR or KIR genotypes on graft survival. Our data do not support the concept that KIR-HLA matching might serve as a tool to improve long-term renal allograft survival. © Copyright 2013 The American Society of Transplantation and the American Society of Transplant Surgeons.Entities:
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Year: 2013 PMID: 23398855 DOI: 10.1111/ajt.12134
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086