Indoleamine 2,3-dioxigenase (IDO) is critical for host resistance against Trypanosoma cruzi

被引:53
作者
Paola Knubel, Carolina [1 ]
Fabian Martinez, Fernando [1 ]
Fretes, Ricardo E. [2 ]
Diaz Lujan, Cintia [2 ]
Gustavo Theumer, Martin [1 ]
Cervi, Laura [1 ]
Cristina Motran, Claudia [1 ]
机构
[1] Univ Nacl Cordoba, Fac Ciencias Quim, Dept Bioquim Clin, Ctr Invest Bioquim Clin & Inmunol CIBICI CONICET, RA-5000 Cordoba, Argentina
[2] Univ Nacl Cordoba, Fac Med, Inst Biol Celular, RA-5000 Cordoba, Argentina
关键词
Infection; parasites; immunomodulation; kynurenines; NECROSIS-FACTOR-ALPHA; NITRIC-OXIDE SYNTHASE; T-CELL PROLIFERATION; INTERFERON-GAMMA; TRYPTOPHAN CATABOLISM; DENDRITIC CELLS; HUMAN-FIBROBLASTS; INTRACELLULAR PATHOGENS; ALTERNATIVE ACTIVATION; TOXOPLASMA-GONDII;
D O I
10.1096/fj.09-150920
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Indoleamine 2,3-dioxigenase (IDO) is an inflammatory cytokine-inducible rate-limiting enzyme of the tryptophan (Trp) catabolism, which is involved in the inhibition of intracellular pathogen replication as well as in immunomodulation. Here we demonstrated the effect of IDO-dependent Trp catabolism on Trypanosoma cruzi resistance to acute infection. Infection with T. cruzi resulted in the systemic activation of IDO. The blocking of IDO activity in vivo impaired resistance to the infection and exacerbated the parasite load and infection-associated pathology. In addition, IDO activity was critical to controlling the parasite's replication in macrophages (Mos), despite the high production of nitric oxide produced by IDO-blocked T. cruzi-infected Mos. Analysis of the mechanisms by which IDO controls the parasite replication revealed that T. cruzi amastigotes were sensitive to L-kynurenine downstream metabolites 3-hydroxykynurenine (3-HK) and 3-hydroxyanthranilic acid, while 3-HK also affected the trypomastigote stage. Finally, 3-HK treatment of mice acutely infected with T. cruzi was able to control the parasite and to improve the survival of lethally infected mice. During infection, IDO played a critical role in host defense against T. cruzi; therefore, the intervention of IDO pathway could be useful as a novel antitrypanosomatid therapeutic strategy.-Knubel, C. P., Martinez, F. F., Fretes, R. E., Diaz Lujan, C., Theumer, M. G., Cervi, L., Motran, C. C. Indoleamine 2,3-dioxigenase (IDO) is critical for host resistance against Trypanosoma cruzi. FASEB J. 24, 2689-2701 (2010). www.fasebj.org
引用
收藏
页码:2689 / 2701
页数:13
相关论文
共 47 条
[1]   Role of indoleamine-2,3-dioxygenase in alpha/beta and gamma interferon-mediated antiviral effects against herpes simplex virus infections [J].
Adams, O ;
Besken, K ;
Oberdörfer, C ;
MacKenzie, CR ;
Takikawa, O ;
Däubener, W .
JOURNAL OF VIROLOGY, 2004, 78 (05) :2632-2636
[2]   PROTECTIVE EFFECT OF PICOLINIC-ACID ON MICE INTRACEREBRALLY INFECTED WITH LETHAL DOSES OF CANDIDA-ALBICANS [J].
BLASI, E ;
MAZZOLLA, R ;
PITZURRA, L ;
BARLUZZI, R ;
BISTONI, F .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (11) :2422-2426
[3]   INDUCTION OF TRYPTOPHAN CATABOLISM IS THE MECHANISM FOR GAMMA-INTERFERON-MEDIATED INHIBITION OF INTRACELLULAR CHLAMYDIA-PSITTACI REPLICATION IN T24 CELLS [J].
BYRNE, GI ;
LEHMANN, LK ;
LANDRY, GJ .
INFECTION AND IMMUNITY, 1986, 53 (02) :347-351
[4]   Impaired production of proinflammatory cytokines and host resistance to acute infection with Trypanosoma cruzi in mice lacking functional myeloid differentiation factor 88 [J].
Campos, MA ;
Closel, M ;
Valente, EP ;
Cardoso, JE ;
Akira, S ;
Alvarez-Leite, JI ;
Ropert, C ;
Gazzinelli, RT .
JOURNAL OF IMMUNOLOGY, 2004, 172 (03) :1711-1718
[5]  
Cerávolo IP, 1999, INFECT IMMUN, V67, P2233
[6]   Inactivation of LRG-47 and IRG-47 reveals a family of interferon γ-inducible genes with essential, pathogen-specific roles in resistance to infection [J].
Collazo, CM ;
Yap, GS ;
Sempowski, GD ;
Lusby, KC ;
Tessarollo, L ;
Woude, GFV ;
Sher, A ;
Taylor, GA .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 194 (02) :181-187
[7]   Inducible nitric oxide synthase is not essential for control of Trypanosoma cruzi infection in mice [J].
Cummings, KL ;
Tarleton, RL .
INFECTION AND IMMUNITY, 2004, 72 (07) :4081-4089
[8]   T cell apoptosis by tryptophan catabolism [J].
Fallarino, I ;
Grohmann, U ;
Vacca, C ;
Bianchi, R ;
Orabona, C ;
Spreca, A ;
Fioretti, MC ;
Puccetti, P .
CELL DEATH AND DIFFERENTIATION, 2002, 9 (10) :1069-1077
[9]   Tryptophan-derived catabolites are responsible for inhibition of T and natural killer cell proliferation induced by indoleamine 2,3-dioxygenase [J].
Frumento, G ;
Rotondo, R ;
Tonetti, M ;
Damonte, G ;
Benatti, U ;
Ferrara, GB .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (04) :459-468
[10]   THE MICROBICIDAL ACTIVITY OF INTERFERON-GAMMA-TREATED MACROPHAGES AGAINST TRYPANOSOMA-CRUZI INVOLVES AN L-ARGININE-DEPENDENT, NITROGEN OXIDE-MEDIATED MECHANISM INHIBITABLE BY INTERLEUKIN-10 AND TRANSFORMING GROWTH-FACTOR-BETA [J].
GAZZINELLI, RT ;
OSWALD, IP ;
HIENY, S ;
JAMES, SL ;
SHER, A .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1992, 22 (10) :2501-2506