IDO and regulatory T cells:: a role for reverse signalling and non-canonical NF-κB activation

被引:388
作者
Puccetti, Paolo
Grohmann, Ursula
机构
[1] Department of Experimental Medicine, Section of Pharmacology, University of Perugia
关键词
D O I
10.1038/nri2163
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The immunoregulatory enzyme indoleamine 2,3-dioxygenase (IDO) suppresses T-cell responses and promotes immune tolerance in mammalian pregnancy, tumour resistance, chronic infection, autoimmunity and allergic inflammation. 'Reverse signalling' and 'non-canonical activation' of the transcription factor nuclear factor-kappa B (NF-kappa B) characterize the peculiar events that occur in dendritic cells when T-cell-engaged ligands work as signalling receptors and culminate in the induction of IDO expression by dendritic cells in an inhibitor of NF-kappa B (I kappa B) kinase-alpha (IKK alpha)-dependent manner. In this Opinion article, we propose that IDO acts as a bridge between dendritic cells and CD4(+) regulatory T cells, and that regulatory T cells use reverse signalling and non-canonical NF-kappa B activation for effector function and self-propagation. This mechanism may also underlie the protective function of glucocorticoids in pathological conditions.
引用
收藏
页码:817 / 823
页数:7
相关论文
共 95 条
[81]   Plasmacytoid DCs and Treg cells:: casual acquaintance or monogamous relationship? [J].
Tang, Qizhi ;
Bluestone, Jeffrey A. .
NATURE IMMUNOLOGY, 2006, 7 (06) :551-553
[82]   Cutting edge:: CD28 controls peripheral homeostasis of CD4+CD25+ [J].
Tang, QZ ;
Henriksen, KJ ;
Boden, EK ;
Tooley, AJ ;
Ye, JQ ;
Subudhi, SK ;
Zheng, XX ;
Strom, TB ;
Bluestone, JA .
JOURNAL OF IMMUNOLOGY, 2003, 171 (07) :3348-3352
[83]  
TAS SW, 2007, BLOOD 0504, DOI DOI 10.1182/BLOOD-2006-11-056010
[84]   RELATIONSHIP BETWEEN INTERFERON-GAMMA, INDOLEAMINE 2,3-DIOXYGENASE, AND TRYPTOPHAN CATABOLISM [J].
TAYLOR, MW ;
FENG, GS .
FASEB JOURNAL, 1991, 5 (11) :2516-2522
[85]   Inhibition of allogeneic T cell proliferation by indoleamine 2,3-dioxygenase-expressing dendritic cells:: Mediation of suppression by tryptophan metabolites [J].
Terness, P ;
Bauer, TM ;
Röse, L ;
Dufter, C ;
Watzlik, A ;
Simon, H ;
Opelz, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (04) :447-457
[86]   Cooperation of Toll-like receptor signals in innate immune defence [J].
Trinchieri, Giorgio ;
Sher, Alan .
NATURE REVIEWS IMMUNOLOGY, 2007, 7 (03) :179-190
[87]   Enhancement of antimicrobial effects by glucocorticoids [J].
Türck, J ;
Oberdörfer, C ;
Vogel, T ;
MacKenzie, CR ;
Däubener, W .
MEDICAL MICROBIOLOGY AND IMMUNOLOGY, 2005, 194 (1-2) :47-53
[88]   Evidence for a tumoral immune resistance mechanism based on tryptophan degradation by indoleamine 2,3-dioxygenase [J].
Uyttenhove, C ;
Pilotte, L ;
Théate, I ;
Stroobant, V ;
Colau, D ;
Parmentier, N ;
Boon, T ;
Van den Eynde, BJ .
NATURE MEDICINE, 2003, 9 (10) :1269-1274
[89]   CD40 ligation prevents onset of tolerogenic properties in human dendritic cells treated with CTLA-4-Ig [J].
Vacca, C ;
Fallarino, F ;
Perruccio, K ;
Orabona, C ;
Bianchi, R ;
Gizzi, S ;
Velardi, A ;
Fioretti, MC ;
Puccetti, P ;
Grohmann, U .
MICROBES AND INFECTION, 2005, 7 (7-8) :1040-1048
[90]   The germless theory of allergic disease: revisiting the hygiene hypothesis [J].
Wills-Karp, M ;
Santeliz, J ;
Karp, CL .
NATURE REVIEWS IMMUNOLOGY, 2001, 1 (01) :69-75