V. Hirsch, H. Steiger, J. Polyomavirus, and B. , Polyomavirus BK, The Lancet Infectious Diseases, vol.3, issue.10, pp.611-623, 2003.
DOI : 10.1016/S1473-3099(03)00770-9

E. Ramos, C. Drachenberg, M. Portocarrero, R. Wali, D. Klassen et al., BK virus nephropathy diagnosis and treatment: experience at the University of Maryland Renal Transplant Program, Clin Transpl, pp.143-153, 2002.

H. Hirsch, W. Knowles, M. Dickenmann, J. Passweg, T. Klimkait et al., Prospective Study of Polyomavirus Type BK Replication and Nephropathy in Renal-Transplant Recipients, New England Journal of Medicine, vol.347, issue.7, pp.488-496, 2002.
DOI : 10.1056/NEJMoa020439

P. Randhawa and D. Brennan, BK Virus Infection in Transplant Recipients: An Overview and Update, American Journal of Transplantation, vol.40, issue.9, pp.2000-2005, 2006.
DOI : 10.1111/j.1600-6143.2005.01137.x

S. Gardner, A. Field, D. Coleman, and B. Hulme, NEW HUMAN PAPOVAVIRUS (B.K.) ISOLATED FROM URINE AFTER RENAL TRANSPLANTATION, The Lancet, vol.297, issue.7712, pp.1253-1257, 1971.
DOI : 10.1016/S0140-6736(71)91776-4

L. Gross, A Filterable Agent, Recovered from Ak Leukemic Extracts, Causing Salivary Gland Carcinomas in C3H Mice., Experimental Biology and Medicine, vol.83, issue.2, pp.414-421, 1953.
DOI : 10.3181/00379727-83-20376

B. Eddy, W. Rowe, J. Hartley, S. Stewart, and R. Huebner, Hemagglutination with the S E polyoma virus, Virology, vol.6, issue.1, pp.290-291, 1958.
DOI : 10.1016/0042-6822(58)90078-3

B. Padgett, D. Walker, G. Zurhein, R. Eckroade, and B. Dessel, CULTIVATION OF PAPOVA-LIKE VIRUS FROM HUMAN BRAIN WITH PROGRESSIVE MULTIFOCAL LEUCOENCEPHALOPATHY, The Lancet, vol.297, issue.7712, pp.1257-1260, 1971.
DOI : 10.1016/S0140-6736(71)91777-6

M. Simon and M. Bressollette-bodin-céline, Le polyomavirus BK. Interactions virus-cellule, réponse immunitaire antivirale, pathogénèse virale, Virologie 2015, vol.19, issue.5

J. Kean, S. Rao, M. Wang, and R. Garcea, Seroepidemiology of human polyomaviruses):e1000363. 11. Knowles W: The epidemiology of BK virus and the occurrence of antigenic and genomic subtypes, Human polyomaviruses: molecular and clinical perspectives, pp.527-559, 2001.

R. Viscidi, D. Rollison, V. Sondak, B. Silver, J. Messina et al., Age-Specific Seroprevalence of Merkel Cell Polyomavirus, BK Virus, and JC Virus, Clinical and Vaccine Immunology, vol.18, issue.10, pp.181737-1743, 2011.
DOI : 10.1128/CVI.05175-11

V. Sroller, E. Hamsikova, V. Ludvikova, P. Vochozkova, M. Kojzarova et al., Seroprevalence rates of BKV, JCV, and MCPyV polyomaviruses in the general Czech Republic population, Journal of Medical Virology, vol.123, issue.9, pp.1560-1568
DOI : 10.1002/jmv.23841

W. Knowles, Discovery and Epidemiology of the Human Polyomaviruses BK Virus (BKV) and JC Virus (JCV), Adv Exp Med Biol, vol.577, pp.19-45, 2006.
DOI : 10.1007/0-387-32957-9_2

H. Zheng, Y. Nishimoto, Q. Chen, M. Hasegawa, S. Zhong et al., Relationships between BK virus lineages and human populations, Microbes and Infection, vol.9, issue.2, pp.204-213, 2007.
DOI : 10.1016/j.micinf.2006.11.008

H. Ikegaya, P. Saukko, R. Tertti, K. Metsarinne, M. Carr et al., Identification of a genomic subgroup of BK polyomavirus spread in European populations, Journal of General Virology, vol.87, issue.11, pp.3201-3208, 2006.
DOI : 10.1099/vir.0.82266-0

T. Takasaka, N. Goya, T. Tokumoto, K. Tanabe, H. Toma et al., Subtypes of BK virus prevalent in Japan and variation in their transcriptional control region, Journal of General Virology, vol.85, issue.10, pp.852821-2827, 2004.
DOI : 10.1099/vir.0.80363-0

Y. Nishimoto, H. Zheng, S. Zhong, H. Ikegaya, Q. Chen et al., An Asian Origin for Subtype IV BK Virus Based on Phylogenetic Analysis, Journal of Molecular Evolution, vol.45, issue.1, pp.103-111, 2007.
DOI : 10.1007/s00239-006-0269-6

L. Jeffers, V. Madden, and J. Webster-cyriaque, BK virus has tropism for human salivary gland cells in vitro: Implications for transmission, Virology, vol.394, issue.2, pp.183-193, 2009.
DOI : 10.1016/j.virol.2009.07.022

J. Goudsmit, P. Wertheim-van-dillen, A. Van-strien, and J. Van-der-noordaa, The role of BK virus in acute respiratory tract disease and the presence of BKV DNA in tonsils, Journal of Medical Virology, vol.128, issue.2, pp.91-99, 1982.
DOI : 10.1002/jmv.1890100203

S. Bofill-mas, M. Formiga-cruz, P. Clemente-casares, F. Calafell, and R. Girones, Potential transmission of human polyomaviruses through the gastrointestinal tract after exposure to virions or viral DNA, J Virol, issue.21, pp.7510290-10299, 2001.

A. Dolei, V. Pietropaolo, E. Gomes, D. Taranto, C. Ziccheddu et al., Polyomavirus persistence in lymphocytes: prevalence in lymphocytes from blood donors and healthy personnel of a blood transfusion centre, Journal of General Virology, vol.81, issue.8, pp.811967-1973, 2000.
DOI : 10.1099/0022-1317-81-8-1967

C. Andrews, K. Shah, R. Daniel, M. Hirsch, and R. Rubin, A Serological Investigation of BK Virus and JC Virus Infections in Recipients of Renal Allografts, Journal of Infectious Diseases, vol.158, issue.1, pp.176-181, 1988.
DOI : 10.1093/infdis/158.1.176

R. Boldorini, S. Allegrini, U. Miglio, A. Paganotti, N. Cocca et al., Serological evidence of vertical transmission of JC and BK polyomaviruses in humans, Journal of General Virology, vol.92, issue.5, pp.921044-1050, 2011.
DOI : 10.1099/vir.0.028571-0

A. Egli, L. Infanti, A. Dumoulin, A. Buser, J. Samaridis et al., Prevalence of Polyomavirus BK and JC Infection and Replication in 400 Healthy Blood Donors, The Journal of Infectious Diseases, vol.199, issue.6, pp.199837-846, 2009.
DOI : 10.1086/597126

C. Polo, J. Perez, A. Mielnichuck, C. Fedele, J. Niubo et al., Prevalence and patterns of polyomavirus urinary excretion in immunocompetent adults and children, Clinical Microbiology and Infection, vol.10, issue.7, pp.640-644, 2004.
DOI : 10.1111/j.1469-0691.2004.00882.x

P. Randhawa, S. Finkelstein, V. Scantlebury, R. Shapiro, C. Vivas et al., HUMAN POLYOMA VIRUS-ASSOCIATED INTERSTITIAL NEPHRITIS IN THE ALLOGRAFT KIDNEY1, Transplantation, vol.67, issue.1, pp.103-109, 1999.
DOI : 10.1097/00007890-199901150-00018

H. Hirsch, D. Brennan, C. Drachenberg, F. Ginevri, J. Gordon et al., Polyomavirus-Associated Nephropathy in Renal Transplantation: Interdisciplinary Analyses and Recommendations, Transplantation, vol.79, issue.10, pp.791277-1286, 2005.
DOI : 10.1097/01.TP.0000156165.83160.09

A. Lanot, N. Bouvier, V. Chatelet, D. J. Bechade, C. Ficheux et al., Hurault de Ligny B: [BK virus infections in kidney transplantation], Nephrol Ther, vol.2016, issue.122, pp.76-85

J. Trofe, J. Gordon, P. Roy-chaudhury, I. Koralnik, W. Atwood et al., Basic and clinical research in polyomavirus nephropathy, Exp Clin Transplant, vol.2, issue.1, pp.162-173, 2004.

J. Trofe, J. Gordon, P. Roy-chaudhury, I. Koralnik, W. Atwood et al., Polyomavirus nephropathy in kidney transplantation, Progress in Transplantation, vol.77, issue.2, pp.130-140, 2004.
DOI : 10.7182/prtr.14.2.6r72583266835340

A. Leung, M. Chan, V. Cheng, A. Lie, K. Yuen et al., Polyoma BK viruria in patients undergoing autologous hematopoietic stem cell transplantation, Bone Marrow Transplantation, vol.30, issue.10, pp.1029-1030, 2005.
DOI : 10.1038/sj.bmt.1704944

H. Hirsch and P. Randhawa, BK Polyomavirus in Solid Organ Transplantation, American Journal of Transplantation, vol.9, issue.Suppl 4, pp.179-188
DOI : 10.1111/ajt.12110

Y. Hwang, J. Sim, A. Leung, A. Lie, and Y. Kwong, BK virus-associated bilateral ureteric stenosis after haematopoietic SCT: viral kinetics and successful treatment, Bone Marrow Transplantation, vol.48, issue.5, pp.745-746
DOI : 10.1016/j.bbmt.2011.03.002

E. Sandler, V. Aquino, E. Goss-shohet, S. Hinrichs, and K. Krisher, BK papova virus pneumonia following hematopoietic stem cell transplantation, Bone Marrow Transplantation, vol.20, issue.2, pp.163-165, 1997.
DOI : 10.1038/sj.bmt.1700849

P. Medeiros, K. Abagge, V. Carvalho, C. Bonfim, and S. Raboni, Polyomavirus BK: Possibly Associated Skin Eruption in a Patient with Hemorrhagic Cystitis, Pediatric Dermatology, vol.98, issue.1, pp.76-77, 2011.
DOI : 10.1111/j.1525-1470.2010.01252.x

L. Jeffers and J. Webster-cyriaque, Viruses and Salivary Gland Disease (SGD): Lessons from HIV SGD, Advances in Dental Research, vol.23, issue.1, pp.79-83, 2011.
DOI : 10.1177/0022034510396882

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3144046

J. Cyriaque, Replication of oral BK virus in human salivary gland cells, J Virol, vol.2014, issue.881, pp.559-573

T. Petrogiannis-haliotis, G. Sakoulas, J. Kirby, I. Koralnik, A. Dvorak et al., BK-Related Polyomavirus Vasculopathy in a Renal-Transplant Recipient, New England Journal of Medicine, vol.345, issue.17, pp.3451250-1255, 2001.
DOI : 10.1056/NEJMoa010319

D. Fioriti, M. Videtta, M. Mischitelli, A. Degener, G. Russo et al., The human polyomavirus BK: Potential role in cancer, Journal of Cellular Physiology, vol.206, issue.2, pp.402-406, 2005.
DOI : 10.1002/jcp.20300

J. Abend, M. Jiang, and M. Imperiale, BK virus and human cancer: Innocent until proven guilty, Seminars in Cancer Biology, vol.19, issue.4, pp.252-260, 2009.
DOI : 10.1016/j.semcancer.2009.02.004

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2694748

D. Sawinski and S. Goral, BK virus infection: an update on diagnosis and treatment, Nephrology Dialysis Transplantation, vol.30, issue.2, pp.209-217
DOI : 10.1093/ndt/gfu023

B. Kasiske, M. Zeier, J. Chapman, J. Craig, H. Ekberg et al., KDIGO clinical practice guideline for the care of kidney transplant recipients: a summary, Kidney International, vol.77, issue.4, pp.299-3111413, 2008.
DOI : 10.1038/ki.2009.377

G. Tylden, H. Hirsch, C. Rinaldo, A. Guasch, P. Roy-chaudhury et al., Brincidofovir (CMX001) inhibits BK polyomavirus replication in primary human urothelial cells Assessment of efficacy and safety of FK778 in comparison with standard care in renal transplant recipients with untreated BK nephropathy, Antimicrob Agents Chemother Transplantation, vol.2015, issue.468, pp.3306-3316, 2010.

G. Knoll, A. Humar, D. Fergusson, O. Johnston, A. House et al., Levofloxacin for BK Virus Prophylaxis Following Kidney Transplantation, JAMA, vol.312, issue.20, pp.3122106-2114
DOI : 10.1001/jama.2014.14721

B. Lee, S. Gabardi, M. Grafals, R. Hofmann, E. Akalin et al., Efficacy of levofloxacin in the treatment of BK viremia: a multicenter, double-blinded, randomized

U. Moens and R. Kkasgl, Molecular biology of BK virus and clinical and basic aspects of BK virus renal infection. Molecular and Clinical perspectives, pp.359-408, 2001.

Y. Yogo, C. Sugimoto, S. Zhong, and Y. Homma, Evolution of the BK polyomavirus: epidemiological, anthropological and clinical implications, Reviews in Medical Virology, vol.79, issue.4, pp.185-199, 2009.
DOI : 10.1002/rmv.613

J. Abend, A. Joseph, D. Das, D. Campbell-cecen, and M. Imperiale, A truncated T antigen expressed from an alternatively spliced BK virus early mRNA, Journal of General Virology, vol.90, issue.5, pp.901238-1245, 2009.
DOI : 10.1099/vir.0.009159-0

O. Gjoerup and Y. Chang, Update on Human Polyomaviruses and Cancer, Adv Cancer Res, vol.106, pp.1-51, 2010.
DOI : 10.1016/S0065-230X(10)06001-X

D. Topalis, G. Andrei, and R. Snoeck, The large tumor antigen: A ???Swiss Army knife??? protein possessing the functions required for the polyomavirus life cycle, Antiviral Research, vol.97, issue.2, pp.122-136, 2013.
DOI : 10.1016/j.antiviral.2012.11.007

J. Low, B. Magnuson, B. Tsai, and M. Imperiale, Identification of Gangliosides GD1b and GT1b as Receptors for BK Virus, Journal of Virology, vol.80, issue.3, pp.1361-1366, 2006.
DOI : 10.1128/JVI.80.3.1361-1366.2006

U. Neu, S. Allen, B. Blaum, Y. Liu, M. Frank et al., A structure-guided mutation in the major capsid protein retargets BK polyomavirus Infection of vero cells by BK virus is dependent on caveolae, PLoS Pathog J Virol, vol.2013, issue.91021, pp.1003688-56, 2004.

T. Moriyama, J. Marquez, T. Wakatsuki, and A. Sorokin, Caveolar Endocytosis Is Critical for BK Virus Infection of Human Renal Proximal Tubular Epithelial Cells, Journal of Virology, vol.81, issue.16, pp.818552-8562, 2007.
DOI : 10.1128/JVI.00924-07

T. Moriyama and A. Sorokin, Intracellular trafficking pathway of BK Virus in human renal proximal tubular epithelial cells, Virology, vol.371, issue.2, pp.336-349, 2008.
DOI : 10.1016/j.virol.2007.09.030

A. Isaacs and J. Lindenmann, Virus Interference. I. The Interferon, Proceedings of the Royal Society B: Biological Sciences, vol.147, issue.927, pp.258-267, 1957.
DOI : 10.1098/rspb.1957.0048

L. Platanias, Mechanisms of type-I- and type-II-interferon-mediated signalling, Nature Reviews Immunology, vol.132, issue.5, pp.375-386, 2005.
DOI : 10.1001/jama.290.24.3222

G. Uze, D. Monneron, L. Prokunina-olsson, B. Muchmore, W. Tang et al., IL-28 and IL-29: newcomers to the interferon family A variant upstream of IFNL3 (IL28B) creating a new interferon gene IFNL4 is associated with impaired clearance of hepatitis C virus, Biochimie Nat Genet, vol.89, issue.452, pp.6-7729, 2007.

F. Siegal, N. Kadowaki, M. Shodell, P. Fitzgerald-bocarsly, K. Shah et al., The Nature of the Principal Type 1 Interferon-Producing Cells in Human Blood, Science, vol.284, issue.5421, pp.1835-1837, 1999.
DOI : 10.1126/science.284.5421.1835

Y. Liu, IPC: Professional Type 1 Interferon-Producing Cells and Plasmacytoid Dendritic Cell Precursors, Annual Review of Immunology, vol.23, issue.1, pp.275-306, 2005.
DOI : 10.1146/annurev.immunol.23.021704.115633

A. Garcia-sastre and C. Biron, Type 1 Interferons and the Virus-Host Relationship: A Lesson in Detente, Science, vol.312, issue.5775, pp.312879-882, 2006.
DOI : 10.1126/science.1125676

C. Samuel, Antiviral Actions of Interferons, Clinical Microbiology Reviews, vol.14, issue.4, pp.778-809, 2001.
DOI : 10.1128/CMR.14.4.778-809.2001

D. Levy and A. Garcia-sastre, The virus battles: IFN induction of the antiviral state and mechanisms of viral evasion, Cytokine & Growth Factor Reviews, vol.12, issue.2-3, pp.143-156, 2001.
DOI : 10.1016/S1359-6101(00)00027-7

C. Sommereyns, S. Paul, P. Staeheli, and T. Michiels, IFN-Lambda (IFN-??) Is Expressed in a Tissue-Dependent Fashion and Primarily Acts on Epithelial Cells In Vivo, PLoS Pathogens, vol.62, issue.3, p.1000017, 2008.
DOI : 10.1371/journal.ppat.1000017.t005

S. Pestka, C. Krause, and M. Walter, Interferons, interferon-like cytokines, and their receptors, Immunological Reviews, vol.11, issue.1, pp.8-32, 2004.
DOI : 10.1107/S0907444999014304

L. Pfeffer, C. Dinarello, R. Herberman, B. Williams, E. Borden et al., Biological properties of recombinant alpha-interferons: 40th anniversary of the discovery of interferons, Cancer Res, issue.12, pp.582489-2499, 1998.

G. Valente, L. Ozmen, F. Novelli, M. Geuna, G. Palestro et al., Distribution of interferon-?? receptor in human tissues, European Journal of Immunology, vol.20, issue.9, pp.2403-2412, 1992.
DOI : 10.1002/eji.1830220933

C. Biron, Interferons ?? and ?? as Immune Regulators???A New Look, Immunity, vol.14, issue.6, pp.661-664, 2001.
DOI : 10.1016/S1074-7613(01)00154-6

URL : http://doi.org/10.1016/s1074-7613(01)00154-6

G. Barber, Cytoplasmic DNA innate immune pathways, Immunological Reviews, vol.107, issue.1, pp.99-108, 2011.
DOI : 10.1111/j.1600-065X.2011.01051.x

W. Schneider, M. Chevillotte, and C. Rice, Interferon-Stimulated Genes: A Complex Web of Host Defenses, Annual Review of Immunology, vol.32, issue.1, pp.513-545, 2014.
DOI : 10.1146/annurev-immunol-032713-120231

B. Lemaitre, E. Nicolas, L. Michaut, J. Reichhart, and J. Hoffmann, The Dorsoventral Regulatory Gene Cassette sp??tzle/Toll/cactus Controls the Potent Antifungal Response in Drosophila Adults, Cell, vol.86, issue.6, pp.973-983, 1996.
DOI : 10.1016/S0092-8674(00)80172-5

T. Kawai and S. Akira, Antiviral Signaling Through Pattern Recognition Receptors, Journal of Biochemistry, vol.141, issue.2, pp.137-145370, 2007.
DOI : 10.1093/jb/mvm032

URL : http://jb.oxfordjournals.org/cgi/content/short/141/2/137

M. Heim and R. Thimme, Innate and adaptive immune responses in HCV infections, Journal of Hepatology, vol.61, issue.1, pp.14-25
DOI : 10.1016/j.jhep.2014.06.035

URL : http://doi.org/10.1016/j.jhep.2014.06.035

Z. Wen, J. Darnell, and J. , Mapping of Stat3 serine phosphorylation to a single residue (727) and evidence that serine phosphorylation has no influence on DNA binding of Stat1 and Stat3, Nucleic Acids Research, vol.25, issue.11, pp.252062-2067, 1997.
DOI : 10.1093/nar/25.11.2062

Z. Wen, Z. Zhong, J. Darnell, J. Varinou, L. Ramsauer et al., Maximal activation of transcription by Stat1 and Stat3 requires both tyrosine and serine phosphorylation Phosphorylation of the Stat1 transactivation domain is required for full-fledged IFN-gamma-dependent innate immunity, Cell Immunity, vol.82, issue.196, pp.241-250793, 1995.

J. Schoggins and C. Rice, Interferon-stimulated genes and their antiviral effector functions, Current Opinion in Virology, vol.1, issue.6, pp.519-525
DOI : 10.1016/j.coviro.2011.10.008

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3274382

S. Der, A. Zhou, B. Williams, and R. Silverman, Identification of genes differentially regulated by interferon alpha, beta, or gamma using oligonucleotide arrays, Proc Natl Acad Sci, issue.26, pp.9515623-15628, 1998.

L. Ivashkiv and L. Donlin, Regulation of type I interferon responses, Nature Reviews Immunology, vol.7, issue.1, pp.36-49
DOI : 10.1038/nri3581

M. Malakhov, O. Malakhova, K. Kim, K. Ritchie, and D. Zhang, UBP43 (USP18) Specifically Removes ISG15 from Conjugated Proteins, Journal of Biological Chemistry, vol.277, issue.12, pp.439976-9981, 2002.
DOI : 10.1074/jbc.M109078200

A. Ribeiro, M. Wornle, N. Motamedi, H. Anders, E. Grone et al., Activation of innate immune defense mechanisms contributes to polyomavirus BK-associated nephropathy, Kidney International, vol.81, issue.1, pp.100-111
DOI : 10.1038/ki.2011.311

J. Abend, J. Low, and M. Imperiale, Inhibitory Effect of Gamma Interferon on BK Virus Gene Expression and Replication, Journal of Virology, vol.81, issue.1, pp.272-279, 2007.
DOI : 10.1128/JVI.01571-06

P. Acott, O. Regan, P. Lee, S. Crocker, and J. , Utilization of Vero Cells for Primary and Chronic BK Virus Infection, Transplantation Proceedings, vol.38, issue.10, pp.3502-3505, 2006.
DOI : 10.1016/j.transproceed.2006.10.163

V. Descamps, E. Martin, V. Morel, C. Francois, F. Helle et al., Comparative Evaluation of Three Nucleic Acid-Based Assays for BK Virus Quantification, Journal of Clinical Microbiology, vol.53, issue.12, pp.533822-3827
DOI : 10.1128/JCM.02116-15

T. Chew, R. Noyce, S. Collins, M. Hancock, and K. Mossman, Characterization of the interferon regulatory factor 3-mediated antiviral response in a cell line deficient for IFN production, Molecular Immunology, vol.46, issue.3, pp.393-399, 2009.
DOI : 10.1016/j.molimm.2008.10.010

S. Anderson, J. Carton, J. Lou, L. Xing, and B. Rubin, Interferon-Induced Guanylate Binding Protein-1 (GBP-1) Mediates an Antiviral Effect against Vesicular Stomatitis Virus and Encephalomyocarditis Virus, Virology, vol.256, issue.1, pp.8-14, 1999.
DOI : 10.1006/viro.1999.9614

URL : http://doi.org/10.1006/viro.1999.9614

Y. Itsui, N. Sakamoto, M. Kurosaki, N. Kanazawa, Y. Tanabe et al., Expressional screening of interferonstimulated genes for antiviral activity against hepatitis C virus replication, J Viral Hepat, issue.10, pp.13690-700, 2006.

D. Vestal and J. Jeyaratnam, The Guanylate-Binding Proteins: Emerging Insights into the Biochemical Properties and Functions of This Family of Large Interferon-Induced Guanosine Triphosphatase, Journal of Interferon & Cytokine Research, vol.31, issue.1, pp.89-97, 2011.
DOI : 10.1089/jir.2010.0102

B. Bodaghi, O. Goureau, D. Zipeto, L. Laurent, J. Virelizier et al., Role of IFNgamma-induced indoleamine 2,3 dioxygenase and inducible nitric oxide synthase in the replication of human cytomegalovirus in retinal pigment epithelial cells, J Immunol, vol.162, issue.2, pp.957-964, 1999.

O. Adams, K. Besken, C. Oberdorfer, C. Mackenzie, O. Takikawa et al., Role of Indoleamine-2,3-Dioxygenase in Alpha/Beta and Gamma Interferon-Mediated Antiviral Effects against Herpes Simplex Virus Infections, Journal of Virology, vol.78, issue.5, pp.782632-2636, 2004.
DOI : 10.1128/JVI.78.5.2632-2636.2004

O. Adams, K. Besken, C. Oberdorfer, C. Mackenzie, D. Russing et al., Inhibition of human herpes simplex virus type 2???by interferon ? and tumor necrosis factor ? is mediated by indoleamine 2,3-dioxygenase, Microbes and Infection, vol.6, issue.9, pp.806-812, 2004.
DOI : 10.1016/j.micinf.2004.04.007

R. Mao, J. Zhang, D. Jiang, D. Cai, J. Levy et al., Indoleamine 2,3-Dioxygenase Mediates the Antiviral Effect of Gamma Interferon against Hepatitis B Virus in Human Hepatocyte-Derived Cells, Journal of Virology, vol.85, issue.2, pp.1048-1057, 2011.
DOI : 10.1128/JVI.01998-10

M. Terajima and A. Leporati, Role of Indoleamine 2,3-Dioxygenase in Antiviral Activity of Interferon-?? Against Vaccinia Virus, Viral Immunology, vol.18, issue.4, pp.722-729, 2005.
DOI : 10.1089/vim.2005.18.722

A. Yeung, W. Wu, M. Freewan, R. Stocker, N. King et al., Flavivirus infection induces indoleamine 2,3-dioxygenase in human monocyte-derived macrophages via tumor necrosis factor and NF-kappaB, J Leukoc Biol, vol.2012, issue.914, pp.657-666

A. Becerra, R. Warke, K. Xhaja, B. Evans, J. Evans et al., Increased activity of indoleamine 2,3-dioxygenase in serum from acutely infected dengue patients linked to gamma interferon antiviral function, Journal of General Virology, vol.90, issue.4, pp.90810-817, 2009.
DOI : 10.1099/vir.0.004416-0

A. Kroger, M. Koster, K. Schroeder, H. Hauser, and P. Mueller, Review: Activities of IRF-1, Journal of Interferon & Cytokine Research, vol.22, issue.1, pp.5-14, 2002.
DOI : 10.1089/107999002753452610

T. Tamura, H. Yanai, D. Savitsky, and T. Taniguchi, The IRF Family Transcription Factors in Immunity and Oncogenesis, Annual Review of Immunology, vol.26, issue.1, pp.535-584, 2008.
DOI : 10.1146/annurev.immunol.26.021607.090400

K. Konan and M. Taylor, Importance of the Two Interferon-stimulated Response Element (ISRE) Sequences in the Regulation of the Human Indoleamine 2,3-Dioxygenase Gene, Journal of Biological Chemistry, vol.271, issue.32, pp.27119140-19145, 1996.
DOI : 10.1074/jbc.271.32.19140

T. Kimura, Y. Kadokawa, H. Harada, M. Matsumoto, M. Sato et al., Essential and non-redundant roles of p48 (ISGF3gamma) and IRF-1 in both type I and type II interferon responses, as revealed by gene targeting studies, Genes to Cells, vol.1, issue.1, pp.115-124, 1996.
DOI : 10.1046/j.1365-2443.1996.08008.x

T. Miki, H. Sun, Y. Lee, A. Tandin, A. Kovscek et al., Blockade of tryptophan catabolism prevents spontaneous tolerogenicity of liver allografts, Transplantation Proceedings, vol.33, issue.1-2, pp.129-130, 2001.
DOI : 10.1016/S0041-1345(00)02792-5

A. Alexander, M. Crawford, S. Bertera, W. Rudert, O. Takikawa et al., Indoleamine 2,3-Dioxygenase Expression in Transplanted NOD Islets Prolongs Graft Survival After Adoptive Transfer of Diabetogenic Splenocytes, Diabetes, vol.51, issue.2, pp.51356-365, 2002.
DOI : 10.2337/diabetes.51.2.356

R. Sucher, K. Fischler, R. Oberhuber, I. Kronberger, C. Margreiter et al., IDO and Regulatory T Cell Support Are Critical for Cytotoxic T Lymphocyte-Associated Ag-4 Ig-Mediated Long-Term Solid Organ Allograft Survival, The Journal of Immunology, vol.188, issue.1, pp.37-46
DOI : 10.4049/jimmunol.1002777

F. Greco, A. Coletti, E. Camaioni, A. Carotti, M. Marinozzi et al., The Janus-faced nature of IDO1 in infectious diseases: challenges and therapeutic opportunities, Future Medicinal Chemistry, vol.8, issue.1, pp.39-54
DOI : 10.4155/fmc.15.165

J. Wilson, E. Lin, C. Pack, E. Frost, A. Hadley et al., Gamma Interferon Controls Mouse Polyomavirus Infection In Vivo, Journal of Virology, vol.85, issue.19, pp.8510126-10134, 2011.
DOI : 10.1128/JVI.00761-11

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3196421

R. Burdeinick-kerr, D. Govindarajan, and D. Griffin, Noncytolytic Clearance of Sindbis Virus Infection from Neurons by Gamma Interferon Is Dependent on Jak/Stat Signaling, Journal of Virology, vol.83, issue.8, pp.3429-3435, 2009.
DOI : 10.1128/JVI.02381-08

M. Trilling, V. Le, J. Rashidi-alavijeh, B. Katschinski, J. Scheller et al., "Activated" STAT Proteins: A Paradoxical Consequence of Inhibited JAK-STAT Signaling in Cytomegalovirus-Infected Cells, The Journal of Immunology, vol.192, issue.1, pp.447-458
DOI : 10.4049/jimmunol.1203516

S. Sohn and P. Hearing, Adenovirus Sequesters Phosphorylated STAT1 at Viral Replication Centers and Inhibits STAT Dephosphorylation, Journal of Virology, vol.85, issue.15, pp.7555-7562, 2011.
DOI : 10.1128/JVI.00513-11

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3147932

D. Vu, P. Sakharkar, T. Shah, R. Naraghi, Q. Yasir et al., Association of Interferon Gamma Gene Polymorphisms With BK Virus Infection Among Hispanic Renal Allograft Recipients, Transplantation, vol.97, issue.6, pp.97660-667
DOI : 10.1097/01.TP.0000438115.20198.89

W. Mulley and D. Nikolic-paterson, Indoleamine 2,3-dioxygenase in transplantation (Review Article), Nephrology, vol.16, issue.3, pp.204-211, 2008.
DOI : 10.1097/01.tp.0000173903.26886.20

U. Hainz, B. Jurgens, and A. Heitger, The role of indoleamine 2,3-dioxygenase in transplantation, Transplant International, vol.16, issue.2, pp.118-127, 2007.
DOI : 10.1111/j.1432-2277.2006.00370.x

V. Mehraj and J. Routy, Tryptophan Catabolism in Chronic Viral Infections: Handling Uninvited Guests, International Journal of Tryptophan Research, vol.8, pp.41-48, 2015.
DOI : 10.4137/IJTR.S26862

URL : http://doi.org/10.4137/ijtr.s26862

Y. Chen, S. Li, Y. He, X. Shi, Y. Chen et al., Immunosuppressive effect of IDO on T cells in patients with chronic hepatitis B, Hepatology Research, vol.361, issue.1, pp.463-468, 2009.
DOI : 10.1111/j.1872-034X.2008.00476.x

K. Higashitani, T. Kanto, S. Kuroda, S. Yoshio, T. Matsubara et al., Association of enhanced activity of indoleamine 2,3-dioxygenase in dendritic cells with the induction of regulatory T cells in chronic hepatitis C infection, Journal of Gastroenterology, vol.179, issue.5, pp.48660-670, 2013.
DOI : 10.1007/s00535-012-0667-z

H. Byakwaga, Y. Boum, Y. Huang, C. Muzoora, A. Kembabazi et al., The Kynurenine Pathway of Tryptophan Catabolism, CD4+ T-Cell Recovery, and Mortality Among HIV-Infected Ugandans Initiating Antiretroviral Therapy, Journal of Infectious Diseases, vol.210, issue.3, pp.210383-391
DOI : 10.1093/infdis/jiu115

M. Sadeghi, I. Lahdou, V. Daniel, P. Schnitzler, G. Fusch et al., Strong association of phenylalanine and tryptophan metabolites with activated cytomegalovirus infection in kidney transplant recipients, Human Immunology, vol.73, issue.2, pp.186-192
DOI : 10.1016/j.humimm.2011.11.002

S. Divanovic, N. Sawtell, A. Trompette, J. Warning, A. Dias et al., Opposing Biological Functions of Tryptophan Catabolizing Enzymes During Intracellular Infection, Journal of Infectious Diseases, vol.205, issue.1, pp.152-161
DOI : 10.1093/infdis/jir621

S. Chon, H. Hassanain, and S. Gupta, Cooperative role of interferon regulatory factor 1 and p91 (STAT1) response elements in interferon-gamma-inducible expression of human indoleamine 2,3-dioxygenase gene, J Biol Chem, issue.29, pp.27117247-17252, 1996.

Y. Jeong, S. Kim, I. Jung, J. Lee, J. Chang et al., Curcumin suppresses the induction of indoleamine 2,3- dioxygenase by blocking the Janus-activated kinase-protein kinase Cdelta- STAT1 signaling pathway in interferon-gamma-stimulated murine dendritic cells, J Biol Chem, issue.6, pp.2843700-3708, 2009.

K. Ramsauer, M. Farlik, G. Zupkovitz, C. Seiser, A. Kroger et al., Distinct modes of action applied by transcription factors STAT1 and IRF1 to initiate transcription of the IFN-gamma-inducible gbp2 gene, Proc Natl Acad Sci, issue.8, pp.1042849-2854, 2007.