TY - JOUR
T1 - Increased pretransplantation plasma kynurenine levels do not protect from but predict acute kidney allograft rejection
AU - Lahdou, Imad
AU - Sadeghi, Mahmoud
AU - Daniel, Volker
AU - Schenk, Martin
AU - Renner, Fabrice
AU - Weimer, Rolf
AU - Löb, Stefan
AU - Schmidt, Jan
AU - Mehrabi, Arianeb
AU - Schnitzler, Paul
AU - Königsrainer, Alfred
AU - Döhler, Bernd
AU - Opelz, Gerhard
AU - Terness, Peter
N1 - Copyright © 2010 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.
PY - 2010/11
Y1 - 2010/11
N2 - Indoleamine 2,3-dioxygenase (IDO), an enzyme expressed in many cell types, catalyses degradation of tryptophan (Trp) to kynurenine (Kyn) and may exert immunosuppressive functions, mediated mainly by kynurenines. Therefore, increased Kyn concentrations would be expected to protect allografts from rejection. We conducted this study to examine whether Kyn has predictive value for kidney graft outcome. End-stage renal disease patients (n = 210) demonstrated an increased Kyn/Trp ratio compared with healthy controls (n = 30). Both Kyn and Trp levels were significantly higher in patients who subsequently developed acute rejection than in patients who did not (p < 0.001 and p < 0.001, respectively). Furthermore, pretransplantation Kyn and Trp plasma concentrations were significantly different in patients who went on to develop acute rejection (high values) or acute tubular necrosis (low values) (p = 0.007 and p = 0.021, respectively). After transplantation Kyn levels decreased. Approximately 3 days before biopsy-confirmed rejection, Kyn was significantly increased in patients with rejection compared with those without rejection (p < 0.001). Contrary to expectation, high Kyn plasma levels before transplantation were not predictive of low rejection risk. Although informative in overall terms, at the present stage, Kyn levels do not allow the concise risk differentiation of individual patients.
AB - Indoleamine 2,3-dioxygenase (IDO), an enzyme expressed in many cell types, catalyses degradation of tryptophan (Trp) to kynurenine (Kyn) and may exert immunosuppressive functions, mediated mainly by kynurenines. Therefore, increased Kyn concentrations would be expected to protect allografts from rejection. We conducted this study to examine whether Kyn has predictive value for kidney graft outcome. End-stage renal disease patients (n = 210) demonstrated an increased Kyn/Trp ratio compared with healthy controls (n = 30). Both Kyn and Trp levels were significantly higher in patients who subsequently developed acute rejection than in patients who did not (p < 0.001 and p < 0.001, respectively). Furthermore, pretransplantation Kyn and Trp plasma concentrations were significantly different in patients who went on to develop acute rejection (high values) or acute tubular necrosis (low values) (p = 0.007 and p = 0.021, respectively). After transplantation Kyn levels decreased. Approximately 3 days before biopsy-confirmed rejection, Kyn was significantly increased in patients with rejection compared with those without rejection (p < 0.001). Contrary to expectation, high Kyn plasma levels before transplantation were not predictive of low rejection risk. Although informative in overall terms, at the present stage, Kyn levels do not allow the concise risk differentiation of individual patients.
KW - Acute Disease
KW - Adult
KW - Aged
KW - Biopsy
KW - Female
KW - Graft Rejection/blood
KW - Humans
KW - Kidney Cortex Necrosis
KW - Kidney Failure, Chronic/blood
KW - Kidney Transplantation
KW - Kynurenine/biosynthesis
KW - Male
KW - Middle Aged
KW - Predictive Value of Tests
KW - Prognosis
KW - Transplantation, Homologous
KW - Tryptophan/biosynthesis
U2 - 10.1016/j.humimm.2010.08.013
DO - 10.1016/j.humimm.2010.08.013
M3 - Original Article
C2 - 20732369
SN - 0198-8859
VL - 71
SP - 1067
EP - 1072
JO - HUMAN IMMUNOLOGY
JF - HUMAN IMMUNOLOGY
IS - 11
ER -