The role of indoleamine 2,3-dioxygenase in the induction of immune tolerance: focus on hematology

被引:210
作者
Curti, Antonio [1 ]
Trabanelli, Sara
Salvestrini, Valentina
Baccarani, Michele
Lemoli, Roberto M.
机构
[1] Univ Bologna, Dept Hematol & Oncol Sci L&A Seragnoli, I-40138 Bologna, Italy
关键词
REGULATORY T-CELLS; MYELOID-LEUKEMIA CELLS; NF-KAPPA-B; PLASMACYTOID DENDRITIC CELLS; CHRONIC MYELOGENOUS LEUKEMIA; DRAINING LYMPH-NODES; NON-HODGKIN-LYMPHOMA; VERSUS-HOST-DISEASE; TRYPTOPHAN CATABOLISM; IFN-GAMMA;
D O I
10.1182/blood-2008-07-144485
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The regulation of the interaction between the immune system and antigens, which may lead to the induction of immune tolerance, is critical both under physiologic conditions and in different pathological settings. In the past few years, major strides have been made in our understanding of the molecular and cellular bases of this process. Novel pathways have been identified and several novel therapeutic agents are currently under clinical investigation for those diseases in which the normal balance between activation and suppression of the immune response is altered. The tryptophan catabolic enzyme, indoleamine 2,3-dioxygenase (IDO), is one of the key players involved in the inhibition of cell proliferation, including that of activated T cells. Recent works have demonstrated a crucial role for IDO in the induction of immune tolerance during infection, pregnancy, transplantation, autoimmunity, and neoplasias, including hematologic malignancies. In this review, the role of IDO in the induction of immunologic tolerance is addressed with a specific focus on its recently discovered effect on hematologic malignancies. (Blood. 2009; 113:2394-2401)
引用
收藏
页码:2394 / 2401
页数:8
相关论文
共 94 条
[1]   Characterization of an indoleamine 2,3-dioxygenase-like protein found in humans and mice [J].
Ball, Helen J. ;
Sanchez-Perez, Angeles ;
Weiser, Silvia ;
Austin, Christopher J. D. ;
Astelbauer, Florian ;
Miu, Jenny ;
McQuillan, James A. ;
Stocker, Roland ;
Jermiin, Lars S. ;
Hunt, Nicholas H. .
GENE, 2007, 396 (01) :203-213
[2]   A key in vivo antitumor mechanism of action of natural product-based brassinins is inhibition of indoleamine 2,3-dioxygenase [J].
Banerjee, T. ;
DuHadaway, J. B. ;
Gaspari, P. ;
Sutanto-Ward, E. ;
Munn, D. H. ;
Mellor, A. L. ;
Malachowski, W. P. ;
Prendergast, G. C. ;
Muller, A. J. .
ONCOGENE, 2008, 27 (20) :2851-2857
[3]   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
[4]   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
[5]   Reduced frequencies and suppressive function of CD4+CD25hi regulatory T cells in patients with chronic lymphocytic leukemia after therapy with fludarabine [J].
Beyer, M ;
Kochanek, M ;
Darabi, K ;
Popov, A ;
Jensen, M ;
Endl, E ;
Knolle, PA ;
Thomas, RK ;
von Bergwelt-Baildon, M ;
Bebey, S ;
Hallek, M ;
Schultze, JL .
BLOOD, 2005, 106 (06) :2018-2025
[6]   In vivo peripheral expansion of naive CD4+CD25high FoxP3+ regulatory T cells in patients with multiple myeloma [J].
Beyer, Marc ;
Kochanek, Matthias ;
Giese, Thomas ;
Endl, Elmar ;
Weihrauch, Martin R. ;
Knolle, Percy A. ;
Classen, Sabine ;
Schultze, Joachim L. .
BLOOD, 2006, 107 (10) :3940-3949
[7]   A crucial role for tryptophan catabolism at the host/Candida albicans interface [J].
Bozza, S ;
Fallarino, F ;
Pitzurra, L ;
Zelante, T ;
Montagnoli, C ;
Bellocchio, S ;
Mosci, P ;
Vacca, C ;
Puccetti, P ;
Romani, L .
JOURNAL OF IMMUNOLOGY, 2005, 174 (05) :2910-2918
[8]   Prognostic value of indoleamine 2,3-dioxygenase expression in colorectal cancer:: Effect on tumor-infiltrating T cells [J].
Brandacher, G ;
Perathoner, A ;
Ladurner, R ;
Schneeberger, S ;
Obrist, P ;
Winkler, C ;
Werner, ER ;
Werner-Felmayer, G ;
Weiss, HG ;
Göbel, G ;
Margreiter, R ;
Königsrainer, A ;
Fuchs, D ;
Amberger, A .
CLINICAL CANCER RESEARCH, 2006, 12 (04) :1144-1151
[9]   Regulation of immune responses by L- arginine metabolism [J].
Bronte, V ;
Zanovello, P .
NATURE REVIEWS IMMUNOLOGY, 2005, 5 (08) :641-654
[10]   Microenvironment produced by acute myeloid leukemia cells prevents T cell activation and proliferation by inhibition of NF-κB, c-myc, and pRb pathways [J].
Buggins, AGS ;
Milojkovic, D ;
Arno, MJ ;
Lea, NC ;
Mufti, GJ ;
Thomas, NSB ;
Hirst, WJR .
JOURNAL OF IMMUNOLOGY, 2001, 167 (10) :6021-6030