Changes in the Serum Levels of Interleukin-17/Interleukin-23 During Acute Rejection in Liver Transplantation

被引:82
作者
Fabrega, Emilio [1 ]
Lopez-Hoyos, Marcos [2 ]
Segundo, David San [2 ]
Casafont, Fernandoo [1 ]
Pons-Romero, Fernando [1 ]
机构
[1] Marques de Valdecilla Univ Hosp, Fac Med, Gastroenterol & Hepatol Unit, Santander 39008, Spain
[2] Marques de Valdecilla Univ Hosp, Fac Med, Immunol Unit, Santander 39008, Spain
关键词
T-LYMPHOCYTES; INTERLEUKIN-17; IL-17; IL-23; CELLS; PROMOTES; IMMUNITY; GENE; BETA;
D O I
10.1002/lt.21724
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Interleukin-23 (IL-23) and T helper 17 (Th17) cells have been cast as major players in autoimmunity, but their role in transplantation immunity remains to be specified. The aim of our study was to investigate the time course of serum levels of IL-23 and IL-17 during hepatic allograft rejection. Serum levels of IL-23 and IL-17 were determined in 20 healthy subjects and 50 hepatic transplant recipients. These patients were divided into 2 groups: group I was composed of 15 patients with acute rejection, and group 11 was composed of 35 patients without acute rejection. Samples were collected on days 1 and 7 after liver transplantation and on the day of liver biopsy. The concentrations of IL-23 were similar for the rejection group and nonrejection group at early postoperative times. We observed a significant increase in serum IL-23 levels in the rejection group when a diagnosis of acute rejection had been established. Similarly to IL-23, at the diagnosis of acute rejection, the concentration of IL-17 was significantly higher in the rejection group versus the nonrejection group. The whole transplant group, including those with stable graft function, had higher serum levels of IL-23 and IL-17 than the controls during the entire postoperative period. In conclusion, IL-23 and IL-17 are up-regulated during acute hepatic rejection. These findings suggest a role for Th17 cells in human liver allograft rejection. Liver Transpl 15:629-633, 2009. (C) 2009 AASLD.
引用
收藏
页码:629 / 633
页数:5
相关论文
共 30 条
[21]   TH1-CELL AND TH2-CELL - DIFFERENT PATTERNS OF LYMPHOKINE SECRETION LEAD TO DIFFERENT FUNCTIONAL-PROPERTIES [J].
MOSMANN, TR ;
COFFMAN, RL .
ANNUAL REVIEW OF IMMUNOLOGY, 1989, 7 :145-173
[22]   Are Th2 helper T lymphocytes beneficial, deleterious, or irrelevant in promoting allograft survival? [J].
Piccotti, JR ;
Chan, SY ;
VanBuskirk, AM ;
Eichwald, EJ ;
Bishop, DK .
TRANSPLANTATION, 1997, 63 (05) :619-624
[23]   Interleukin-17 antagonism inhibits acute but not chronic vascular rejection [J].
Tang, JL ;
Subbotin, VM ;
Antonysamy, MA ;
Troutt, AB ;
Rao, AS ;
Thomson, AW .
TRANSPLANTATION, 2001, 72 (02) :348-350
[24]  
Van Kooten C, 1998, J AM SOC NEPHROL, V9, P1526
[25]   The role of interleukin-17 during acute rejection after lung transplantation [J].
Vanaudenaerde, BM ;
Dupont, LJ ;
Wuyts, WA ;
Verbeken, E ;
Meyts, I ;
Bullens, DM ;
Dilissen, E ;
Luyts, L ;
Van Raemdonck, DE ;
Verleden, GM .
EUROPEAN RESPIRATORY JOURNAL, 2006, 27 (04) :779-787
[26]   Transfusion of polarized TH2-like cell populations into SCID mouse cardiac allograft recipients results in acute allograft rejection [J].
VanBuskirk, AM ;
Wakely, ME ;
Orosz, CG .
TRANSPLANTATION, 1996, 62 (02) :229-238
[27]   Human IL-23-producing type 1 macrophages promote but IL-10-producing type 2, macrophages subvert, immunity to (myco)bacteria [J].
Verreck, FAW ;
de Boer, T ;
Langenberg, DML ;
Hoeve, MA ;
Kramer, M ;
Vaisberg, E ;
Kastelein, R ;
Kolk, A ;
de Waal-Malefyt, R ;
Ottenhoff, THM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (13) :4560-4565
[28]   A critical function for transforming growth factor-β, interleukin 23 and proinflammatory cytokines in driving and modulating human TH-17 responses [J].
Volpe, Elisabetta ;
Servant, Nicolas ;
Zollinger, Raphael ;
Bogiatzi, Sofia I. ;
Hupe, Philippe ;
Barillot, Emmanuel ;
Soumelis, Vassili .
NATURE IMMUNOLOGY, 2008, 9 (06) :650-657
[29]  
YOO ZB, 1995, J IMMUNOL, V155, P5483
[30]   Anti-type V collagen lymphocytes that express IL-17 and IL-23 induce rejection pathology in fresh and well-healed lung transplants [J].
Yoshida, S ;
Haque, A ;
Mizobuchi, T ;
Iwata, T ;
Chiyo, M ;
Webb, TJ ;
Baldridge, LA ;
Heidler, KM ;
Cummings, OW ;
Fujisawa, T ;
Blum, JS ;
Brand, DD ;
Wilkes, DS .
AMERICAN JOURNAL OF TRANSPLANTATION, 2006, 6 (04) :724-735