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10.1111/ajt.12147

http://scihub22266oqcxt.onion/10.1111/ajt.12147
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C4412610!4412610!23433356
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suck abstract from ncbi


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pmid23433356      Am+J+Transplant 2013 ; 13 (4): 954-60
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  • Class II Alloantibody and Mortality in Simultaneous Liver-Kidney Transplantation #MMPMID23433356
  • O?Leary JG; Gebel HM; Ruiz R; Bray RA; Marr JD; Zhou XJ; Shiller SM; Susskind BM; Kirk AD; Klintmalm GB
  • Am J Transplant 2013[Apr]; 13 (4): 954-60 PMID23433356show ga
  • 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 (pre-formed 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.
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