Indoleamine 2,3-dioxygenase, tumor-induced tolerance and counter-regulation

被引:134
作者
Munn, DH [1 ]
机构
[1] Med Coll Georgia, Immunotherapy Ctr, Augusta, GA 30912 USA
[2] Med Coll Georgia, Dept Pediat, Augusta, GA 30912 USA
关键词
D O I
10.1016/j.coi.2006.01.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Tumors create an abnormal state of tolerance toward themselves and their antigens. One mechanism that might contribute to this tolerance is the immunoregulatory enzyme indoleamine 2,3-dioxygenase (IDO). IDO-expressing antigen-presenting cells are found in tumor-draining lymph nodes, where they can create a tolerogenic microenvironment. IDO can also be expressed within the tumor itself, by tumor cells or host stromal cells, where it can inhibit the effector phase the immune response. Finally, emerging evidence suggests that IDO might also constitute a significant counter-regulatory mechanism, induced by clinically relevant pro-inflammatory signals, such as IFN-gamma, IFN-alpha, CpG oligodeoxynucleoticles, and 4-1BB ligation. Strategies to inhibit the IDO pathway may thus assist in breaking tolerance to tumors, and might enhance the efficacy of other immunotherapy strategies by removing unwanted counter-regulation.
引用
收藏
页码:220 / 225
页数:6
相关论文
共 48 条
[1]   INHIBITION OF TUMOR-CELL GROWTH BY INTERFERON-GAMMA IS MEDIATED BY 2 DISTINCT MECHANISMS DEPENDENT UPON OXYGEN-TENSION - INDUCTION OF TRYPTOPHAN DEGRADATION AND DEPLETION OF INTRACELLULAR NICOTINAMIDE ADENINE-DINUCLEOTIDE [J].
AUNE, TM ;
POGUE, SL .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (03) :863-875
[2]   A minor population of splenic dendritic cells expressing CD19 mediates IDO-dependent T cell suppression via type IIFN signaling following B7 ligation [J].
Baban, B ;
Hansen, AM ;
Chandler, PR ;
Manlapat, A ;
Bingaman, A ;
Kahler, DJ ;
Munn, DH ;
Mellor, AL .
INTERNATIONAL IMMUNOLOGY, 2005, 17 (07) :909-919
[3]  
Barceló-Batllori S, 2002, PROTEOMICS, V2, P551, DOI 10.1002/1615-9861(200205)2:5<551::AID-PROT551>3.0.CO
[4]  
2-O
[5]   A two-step induction of indoleamine 2,3 dioxygenase (IDO) activity during dendritic-cell maturation [J].
Braun, D ;
Longman, RS ;
Albert, ML .
BLOOD, 2005, 106 (07) :2375-2381
[6]   Modulation of tryptophan catabolism by regulatory T cells [J].
Fallarino, F ;
Grohmann, U ;
Hwang, KW ;
Orabona, C ;
Vacca, C ;
Bianchi, R ;
Belladonna, ML ;
Fioretti, MC ;
Alegre, ML ;
Puccetti, P .
NATURE IMMUNOLOGY, 2003, 4 (12) :1206-1212
[7]  
Gajewski Thomas F, 2004, Curr Opin Investig Drugs, V5, P1279
[8]   A defect in tryptophan catabolism impairs tolerance in nonobese diabetic mice [J].
Grohmann, U ;
Fallarino, F ;
Bianchi, R ;
Orabona, C ;
Vacca, C ;
Fioretti, MC ;
Puccetti, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 198 (01) :153-160
[9]   IL-6 inhibits the tolerogenic function of CD8α+ dendritic cells expressing indoleamine 2,3-dioxygenase [J].
Grohmann, U ;
Fallarino, F ;
Bianchi, R ;
Belladonna, ML ;
Vacca, C ;
Orabona, C ;
Uyttenhove, C ;
Fioretti, MC ;
Puccetti, P .
JOURNAL OF IMMUNOLOGY, 2001, 167 (02) :708-714
[10]   Inhibition of indoleamine 2,3-dioxygenase augments trinitrobenzene sulfonic acid colitis in mice [J].
Gurtner, GJ ;
Newberry, RD ;
Schloemann, SR ;
McDonald, KG ;
Stenson, WF .
GASTROENTEROLOGY, 2003, 125 (06) :1762-1773