| Literature DB >> 23433356 |
J G O'Leary1, H M Gebel2, R Ruiz1, R A Bray2, J D Marr1, X J Zhou3, S M Shiller3, B M Susskind1, A D Kirk4, G B Klintmalm1.
Abstract
Hyperacute kidney rejection is unusual in crossmatch positive recipients of simultaneous liver-kidney transplants (SLKT). However, recent data suggest that these patients remain at risk for antibody-mediated kidney rejection. To further investigate the risk associated with donor-specific alloantibodies (DSA) in SLKT, we studied 86 consecutive SLKT patients with an available pre-SLKT serum sample. Serum samples were analyzed in a blinded fashion for HLA DSA using single antigen beads (median florescence intensity≥2,000=positive). Post-SLKT samples were analyzed when available (76%). Thirty patients had preformed DSA, and nine developed de novo DSA. Preformed class I DSA did not change the risk of rejection, patient or allograft survival. In contrast, preformed class II DSA was associated with a markedly increased risk of renal antibody mediated rejection (AMR) (p=0.006), liver allograft rejection (p=0.002), patient death (p=0.02), liver allograft loss (p=0.02) and renal allograft loss (p=0.045). Multivariable modeling showed class II DSA (preformed or de novo) to be an independent predictor of patient death (HR=2.2; p=0.043) and liver allograft loss (HR=2.2; p=0.044). These data warrant reconsideration of the approach to DSA in SLKT. © Copyright 2013 The American Society of Transplantation and the American Society of Transplant Surgeons.Entities:
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Year: 2013 PMID: 23433356 PMCID: PMC4412610 DOI: 10.1111/ajt.12147
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086