The role of indoleamine 2,3-dioxygenase in transplantation

被引:42
作者
Hainz, Ursula [1 ]
Juergens, Birgit [1 ]
Heitger, Andreas [1 ]
机构
[1] Childrens Canc Res Inst, A-1090 Vienna, Austria
关键词
CTLA-4-Ig; IDO; immunoregulation; tolerance; transplantation;
D O I
10.1111/j.1432-2277.2006.00370.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
Indoleamine 2,3-dioxygenase (IDO), by enzymatic tryptophan degradation, has recently been proposed to have profound immunoregulatory activity. By most recent findings IDO induction follows reverse signaling of cytotoxic T-lymphocyte antigen-4 (CTLA-4) to its ligands CD80/86 and acts as a counter-regulatory mechanism to T-cell stimulation. With regard to transplantation, experimental evidence suggests that IDO has the potential to down-regulate allo-responses of T cells in vitro and to promote tolerance in murine models of pancreatic islet transplantation and of allogeneic T-cell transfer in vivo. However, the physiologic role of IDO in human organ transplantation still is to be elucidated. Experiments that clearly identify a significance of IDO in tolerance induction to vascularized organ allografts or in effecting costimulation blockade are required. In this review we provide a conceptual view of the current knowledge of IDO in the context of transplantation and, in light of its particular biological features, speculate about its potential application in novel therapeutic approaches for tolerance induction.
引用
收藏
页码:118 / 127
页数:10
相关论文
共 73 条
[1]   Indoleamine 2,3-dioxygenase expression in trans-planted NOD islets prolongs graft survival after adoptive transfer of diabetogenic splenocytes [J].
Alexander, AM ;
Crawford, M ;
Bertera, S ;
Rudert, WA ;
Takikawa, O ;
Robbins, PD ;
Trucco, M .
DIABETES, 2002, 51 (02) :356-365
[2]   Eosinophil granulocytes account for indoleamine 2,3-dioxygenase-mediated immune escape in human non-small cell lung cancer [J].
Astigiano, S ;
Morandi, B ;
Costa, R ;
Mastracci, L ;
D'Agostino, A ;
Ratto, GB ;
Melioli, G ;
Frumento, G .
NEOPLASIA, 2005, 7 (04) :390-396
[3]   Chronic inflammation, immunosuppression and cancer: New insights and outlook [J].
Baniyash, M .
SEMINARS IN CANCER BIOLOGY, 2006, 16 (01) :80-88
[4]   Studying the immunosuppressive role of indoleamine 2,3-dioxygenase:: tryptophan metabolites suppress rat allogeneic T-cell responses in vitro and in vivo [J].
Bauer, TM ;
Jiga, LP ;
Chuang, JJ ;
Randazzo, M ;
Opelz, G ;
Terness, P .
TRANSPLANT INTERNATIONAL, 2005, 18 (01) :95-100
[5]   TRYPTOPHAN DEPLETION AS A MECHANISM OF GAMMA-INTERFERON-MEDIATED CHLAMYDIAL PERSISTENCE [J].
BEATTY, WL ;
BELANGER, TA ;
DESAI, AA ;
MORRISON, RP ;
BYRNE, GI .
INFECTION AND IMMUNITY, 1994, 62 (09) :3705-3711
[6]   Expression of indoleamine 2,3-dioxygenase (IDO) by endothelial cells: Implications for the control of alloresponses [J].
Beutelspacher, SC ;
Tan, PH ;
McClure, MO ;
Larkin, DFP ;
Lechler, RI ;
George, AJT .
AMERICAN JOURNAL OF TRANSPLANTATION, 2006, 6 (06) :1320-1330
[7]   CTLA41g: Bridging the basic immunology with clinical application [J].
Bluestone, JA ;
St Clair, EW ;
Turka, LA .
IMMUNITY, 2006, 24 (03) :233-238
[8]   Sustained exposure to bacterial antigen induces interferon-γ-dependent T cell receptor down-regulation and impaired T cell function [J].
Bronstein-Sitton, N ;
Cohen-Daniel, L ;
Vaknin, I ;
Ezernitchi, AV ;
Leshem, B ;
Halabi, A ;
Houri-Hadad, Y ;
Greenbaum, E ;
Zakay-Rones, Z ;
Shapira, L ;
Baniyash, M .
NATURE IMMUNOLOGY, 2003, 4 (10) :957-964
[9]  
BROWN RR, 1991, ADV EXP MED BIOL, V294, P425
[10]   LOCALIZATION OF THE HUMAN INDOLEAMINE 2,3-DIOXYGENASE (IDO) GENE TO THE PERICENTROMERIC REGION OF HUMAN CHROMOSOME-8 [J].
BURKIN, DJ ;
KIMBRO, KS ;
BARR, BL ;
JONES, C ;
TAYLOR, MW ;
GUPTA, SL .
GENOMICS, 1993, 17 (01) :262-263