S. Bhatt, P. Gething, O. Brady, J. Messina, A. Farlow et al., The global distribution and burden of dengue, Nature, vol.62, issue.7446, pp.504-507, 2013.
DOI : 10.1016/S0065-308X(05)62004-0

A. Blasius, M. Cella, J. Maldonado, T. Takai, and M. Colonna, Siglec-H is an IPC-specific receptor that modulates type I IFN secretion through DAP12, Blood, vol.107, issue.6, pp.2474-2476, 2006.
DOI : 10.1182/blood-2005-09-3746
URL : http://www.bloodjournal.org/content/bloodjournal/107/6/2474.full.pdf

A. Carlin, E. Plummer, E. Vizcarra, N. Sheets, Y. Joo et al., An IRF-3-, IRF-5-, and IRF-7-Independent Pathway of Dengue Viral Resistance Utilizes IRF-1 to Stimulate Type I and II Interferon Responses, Cell Reports, vol.21, issue.6, pp.1600-1612, 2017.
DOI : 10.1016/j.celrep.2017.10.054
URL : https://doi.org/10.1016/j.celrep.2017.10.054

H. Chen, K. King, J. Tu, M. Sanchez, A. Luster et al., The Roles of IRF-3 and IRF-7 in Innate Antiviral Immunity against Dengue Virus, The Journal of Immunology, vol.191, issue.8, pp.4194-4201, 2013.
DOI : 10.4049/jimmunol.1300799

H. Chen, F. Hofman, J. Kung, Y. Lin, and B. Wu-hsieh, Both Virus and Tumor Necrosis Factor Alpha Are Critical for Endothelium Damage in a Mouse Model of Dengue Virus-Induced Hemorrhage, Journal of Virology, vol.81, issue.11, pp.5518-5526, 2007.
DOI : 10.1128/JVI.02575-06

V. Costa, W. Ye, Q. Chen, M. Teixeira, P. Preiser et al., ABSTRACT, mBio, vol.8, issue.4, pp.741-1700741, 2017.
DOI : 10.1128/mBio.00741-17
URL : https://hal.archives-ouvertes.fr/hal-01377557

B. De-chassey, A. Aublin-gex, A. Ruggieri, L. Meyniel-schicklin, F. Pradezynski et al., The Interactomes of Influenza Virus NS1 and NS2 Proteins Identify New Host Factors and Provide Insights for ADAR1 Playing a Supportive Role in Virus Replication, PLoS Pathogens, vol.94, issue.7, p.23853584, 2013.
DOI : 10.1371/journal.ppat.1003440.s005

D. Prete, A. Luganini, A. Scutera, S. Rossi, S. Anselmo et al., Interferon-?? Production by Plasmacytoid Dendritic Cells Is Dispensable for an Effective Anti-Cytomegalovirus Response in Adaptor Protein-3-Deficient Mice, Journal of Interferon & Cytokine Research, vol.35, issue.3, pp.232-238, 2015.
DOI : 10.1089/jir.2013.0110

C. Dental, J. Florentin, B. Aouar, F. Gondois-rey, D. Durantel et al., Hepatitis C Virus Fails To Activate NF-??B Signaling in Plasmacytoid Dendritic Cells, Journal of Virology, vol.86, issue.2, pp.1090-1096, 2012.
DOI : 10.1128/JVI.05444-11
URL : http://jvi.asm.org/content/86/2/1090.full.pdf

E. Dé-cembre, S. Assil, M. Hillaire, W. Dejnirattisai, J. Mongkolsapaya et al., Sensing of immature particles produced by dengue virus infected cells induces an antiviral response by plasmacytoid dendritic cells, PLoS Pathogens, vol.10, p.25340500, 2014.

M. Dreux, U. Garaigorta, B. Boyd, E. Dé-cembre, J. Chung et al., Short-Range Exosomal Transfer of Viral RNA from Infected Cells to Plasmacytoid Dendritic Cells Triggers Innate Immunity, Cell Host & Microbe, vol.12, issue.4, pp.558-570, 2012.
DOI : 10.1016/j.chom.2012.08.010
URL : https://doi.org/10.1016/j.chom.2012.08.010

L. Dupuis-maguiraga, M. Noret, S. Brun, L. Grand, R. Gras et al., Chikungunya Disease: Infection-Associated Markers from the Acute to the Chronic Phase of Arbovirus-Induced Arthralgia, PLoS Neglected Tropical Diseases, vol.38, issue.39, p.22479654, 2012.
DOI : 10.1371/journal.pntd.0001446.t003

J. Freaney, R. Kim, R. Mandhana, and C. Horvath, Extensive Cooperation of Immune Master Regulators IRF3 and NF??B in RNA Pol II Recruitment and Pause Release in Human Innate Antiviral Transcription, Cell Reports, vol.4, issue.5, pp.959-973, 2013.
DOI : 10.1016/j.celrep.2013.07.043

A. García-sastre, Ten Strategies of Interferon Evasion by Viruses, Cell Host & Microbe, vol.22, issue.2, pp.176-184, 2017.
DOI : 10.1016/j.chom.2017.07.012

C. Gardner, C. Burke, S. Higgs, W. Klimstra, and K. Ryman, Interferon-alpha/beta deficiency greatly exacerbates arthritogenic disease in mice infected with wild-type chikungunya virus but not with the cell culture-adapted live-attenuated 181/25 vaccine candidate, Virology, vol.425, issue.2, p.22305131, 2012.
DOI : 10.1016/j.virol.2011.12.020
URL : https://doi.org/10.1016/j.virol.2011.12.020

C. Geurtsvankessel, M. Willart, L. Van-rijt, F. Muskens, M. Kool et al., but not plasmacytoid dendritic cells, The Journal of Experimental Medicine, vol.73, issue.7, pp.1621-1634, 2008.
DOI : 10.1017/S0022172400069412

D. Gough, N. Messina, C. Clarke, R. Johnstone, and D. Levy, Constitutive Type I Interferon Modulates Homeostatic Balance through Tonic Signaling, Immunity, vol.36, issue.2, pp.166-174, 2012.
DOI : 10.1016/j.immuni.2012.01.011
URL : https://doi.org/10.1016/j.immuni.2012.01.011

C. Guillerey, J. Mouriè-s, G. Polo, N. Doyen, H. Law et al., Pivotal role of plasmacytoid dendritic cells in inflammation and NK-cell responses after TLR9 triggering in mice, Blood, vol.120, issue.1, pp.90-99, 2012.
DOI : 10.1182/blood-2012-02-410936

J. Hall, L. Casciola-rosen, A. Berger, E. Kapsogeorgou, C. Cheadle et al., Precise probes of type II interferon activity define the origin of interferon signatures in target tissues in rheumatic diseases, Proceedings of the National Academy of Sciences, vol.56, issue.8, pp.17609-17614, 2012.
DOI : 10.1002/art.22790

H. Hoffmann, W. Schneider, and C. Rice, Interferons and viruses: an evolutionary arms race of molecular interactions, Trends in Immunology, vol.36, issue.3, pp.124-138, 2015.
DOI : 10.1016/j.it.2015.01.004
URL : http://europepmc.org/articles/pmc4384471?pdf=render

K. Honda, H. Yanai, H. Negishi, M. Asagiri, M. Sato et al., IRF-7 is the master regulator of type-I interferon-dependent immune responses, Nature, vol.4, issue.7034, pp.772-777, 2005.
DOI : 10.1038/ni978

M. Iwanaszko and M. Kimmel, NF-??B and IRF pathways: cross-regulation on target genes promoter level, BMC Genomics, vol.20, issue.17, pp.307-25888367, 2015.
DOI : 10.1128/MCB.20.17.6342-6353.2000
URL : https://bmcgenomics.biomedcentral.com/track/pdf/10.1186/s12864-015-1511-7?site=bmcgenomics.biomedcentral.com

G. Jego, A. Palucka, J. Blanck, C. Chalouni, V. Pascual et al., Plasmacytoid Dendritic Cells Induce Plasma Cell Differentiation through Type I Interferon and Interleukin 6, Immunity, vol.19, issue.2, pp.225-234, 1016.
DOI : 10.1016/S1074-7613(03)00208-5
URL : https://doi.org/10.1016/s1074-7613(03)00208-5

S. Jensen and A. Thomsen, Sensing of RNA Viruses: a Review of Innate Immune Receptors Involved in Recognizing RNA Virus Invasion, Journal of Virology, vol.86, issue.6, pp.2900-291005738, 1128.
DOI : 10.1128/JVI.05738-11

N. Jewell, N. Vaghefi, S. Mertz, P. Akter, R. Peebles et al., Differential Type I Interferon Induction by Respiratory Syncytial Virus and Influenza A Virus In Vivo, Journal of Virology, vol.81, issue.18, pp.9790-980000530, 1128.
DOI : 10.1128/JVI.00530-07
URL : http://jvi.asm.org/content/81/18/9790.full.pdf

S. Kang, H. Liang, B. Reizis, and R. Locksley, Regulation of Hierarchical Clustering and Activation of Innate Immune Cells by Dendritic Cells, Immunity, vol.29, issue.5, pp.819-833, 2008.
DOI : 10.1016/j.immuni.2008.09.017
URL : https://doi.org/10.1016/j.immuni.2008.09.017

Y. Kumagai, O. Takeuchi, H. Kato, H. Kumar, K. Matsui et al., Alveolar Macrophages Are the Primary Interferon-?? Producer in Pulmonary Infection with RNA Viruses, Immunity, vol.27, issue.2, pp.240-252, 2007.
DOI : 10.1016/j.immuni.2007.07.013
URL : https://doi.org/10.1016/j.immuni.2007.07.013

H. Lazear, A. Lancaster, C. Wilkins, M. Suthar, A. Huang et al., IRF-3, IRF-5, and IRF-7 coordinately regulate the type I IFN response in myeloid dendritic cells downstream of MAVS signaling, PLoS Pathogens, vol.9, p.23300459, 2013.

S. Liu, D. Sanchez, R. Aliyari, S. Lu, and G. Cheng, Systematic identification of type I and type II interferon-induced antiviral factors, Proceedings of the National Academy of Sciences, vol.19, issue.2, pp.4239-4244, 2012.
DOI : 10.1093/bioinformatics/19.2.295
URL : http://www.pnas.org/content/109/11/4239.full.pdf

H. Phipps-yonas, J. Seto, S. Sealfon, T. Moran, and A. Fernandez-sesma, Interferon-beta pretreatment of conventional and plasmacytoid human dendritic cells enhances their activation by influenza virus, PLoS Pathogens, vol.4, p.18974865, 2008.
DOI : 10.1371/journal.ppat.1000193
URL : https://doi.org/10.1371/journal.ppat.1000193

M. Pryor, J. Carr, H. Hocking, A. Davidson, P. Li et al., Replication of dengue virus type 2 in human monocyte-derived macrophages: comparisons of isolates and recombinant viruses with substitutions at amino acid 390 in the envelope glycoprotein., The American Journal of Tropical Medicine and Hygiene, vol.65, issue.5, pp.427-434, 2001.
DOI : 10.4269/ajtmh.2001.65.427

F. Puttur, C. Arnold-schrauf, K. Lahl, G. Solmaz, M. Lindenberg et al., Absence of Siglec-H in MCMV Infection Elevates Interferon Alpha Production but Does Not Enhance Viral Clearance, PLoS Pathogens, vol.264, issue.9, p.24086137, 2013.
DOI : 10.1371/journal.ppat.1003648.s003
URL : https://doi.org/10.1371/journal.ppat.1003648

D. Rissin, C. Kan, T. Campbell, S. Howes, D. Fournier et al., Single-molecule enzyme-linked immunosorbent assay detects serum proteins at subfemtomolar concentrations, Nature Biotechnology, vol.8, issue.6, pp.595-599, 2010.
DOI : 10.1038/nbt.1641
URL : http://europepmc.org/articles/pmc2919230?pdf=render

P. Rudd, J. Wilson, J. Gardner, T. Larcher, C. Babarit et al., Interferon Response Factors 3 and 7 Protect against Chikungunya Virus Hemorrhagic Fever and Shock, Journal of Virology, vol.86, issue.18, pp.9888-989800956, 2012.
DOI : 10.1128/JVI.00956-12
URL : https://hal.archives-ouvertes.fr/hal-01191139

C. Schilte, M. Buckwalter, M. Laird, M. Diamond, O. Schwartz et al., Cutting Edge: Independent Roles for IRF-3 and IRF-7 in Hematopoietic and Nonhematopoietic Cells during Host Response to Chikungunya Infection, The Journal of Immunology, vol.188, issue.7, pp.2967-2971, 2012.
DOI : 10.4049/jimmunol.1103185
URL : https://hal.archives-ouvertes.fr/pasteur-01372485

C. Schilte, T. Couderc, F. Chretien, M. Sourisseau, N. Gangneux et al., Type I IFN controls chikungunya virus via its action on nonhematopoietic cells, The Journal of Experimental Medicine, vol.58, issue.2, pp.429-442, 2010.
DOI : 10.1038/77553
URL : https://hal.archives-ouvertes.fr/pasteur-00458108

M. Schmid and E. Harris, Monocyte Recruitment to the Dermis and Differentiation to Dendritic Cells Increases the Targets for Dengue Virus Replication, PLoS Pathogens, vol.595, issue.12, p.25474197, 2014.
DOI : 10.1371/journal.ppat.1004541.s005
URL : https://doi.org/10.1371/journal.ppat.1004541

J. Schulthess, B. Meresse, E. Ramiro-puig, N. Montcuquet, S. Darche et al., Interleukin-15-Dependent NKp46+ Innate Lymphoid Cells Control Intestinal Inflammation by Recruiting Inflammatory Monocytes, Immunity, vol.37, issue.1, pp.108-121, 2012.
DOI : 10.1016/j.immuni.2012.05.013
URL : https://doi.org/10.1016/j.immuni.2012.05.013

S. Seo, H. Kwon, H. Ko, Y. Byun, B. Seong et al., Type I interferon signaling regulates Ly6C(hi) monocytes and neutrophils during acute viral pneumonia in mice, PLoS Pathogens, vol.7, p.21383977, 2011.
DOI : 10.1371/journal.ppat.1001304
URL : http://doi.org/10.1371/journal.ppat.1001304

S. Shresta, J. Kyle, H. Snider, M. Basavapatna, P. Beatty et al., Interferon-Dependent Immunity Is Essential for Resistance to Primary Dengue Virus Infection in Mice, Whereas T- and B-Cell-Dependent Immunity Are Less Critical, Journal of Virology, vol.78, issue.6, pp.2701-2710, 2004.
DOI : 10.1128/JVI.78.6.2701-2710.2004
URL : http://jvi.asm.org/content/78/6/2701.full.pdf

M. Swiecki and M. Colonna, The multifaceted biology of plasmacytoid dendritic cells, Nature Reviews Immunology, vol.9, issue.8, pp.471-485, 2015.
DOI : 10.1038/ni.1669
URL : http://europepmc.org/articles/pmc4808588?pdf=render

M. Swiecki, S. Gilfillan, W. Vermi, Y. Wang, and M. Colonna, Plasmacytoid Dendritic Cell Ablation Impacts Early Interferon Responses and Antiviral NK and CD8+ T Cell Accrual, Immunity, vol.33, issue.6, pp.955-966, 2010.
DOI : 10.1016/j.immuni.2010.11.020
URL : https://doi.org/10.1016/j.immuni.2010.11.020

M. Swiecki, Y. Wang, S. Gilfillan, and M. Colonna, Plasmacytoid Dendritic Cells Contribute to Systemic but Not Local Antiviral Responses to HSV Infections, PLoS Pathogens, vol.294, issue.10, p.24204273, 2013.
DOI : 10.1371/journal.ppat.1003728.g006
URL : https://doi.org/10.1371/journal.ppat.1003728

H. Takagi, T. Fukaya, K. Eizumi, Y. Sato, K. Sato et al., Plasmacytoid Dendritic Cells Are Crucial for the Initiation of Inflammation and T Cell Immunity In??Vivo, Immunity, vol.35, issue.6, pp.958-971, 2011.
DOI : 10.1016/j.immuni.2011.10.014
URL : https://hal.archives-ouvertes.fr/hal-00665515

E. Tomasello, E. Pollet, V. Manh, T. Uzé, G. Dalod et al., Harnessing Mechanistic Knowledge on Beneficial Versus Deleterious IFN-I Effects to Design Innovative Immunotherapies Targeting Cytokine Activity to Specific Cell Types, Frontiers in Immunology, vol.47, issue.46, p.25400632, 2014.
DOI : 10.1021/bi801588g
URL : https://hal.archives-ouvertes.fr/hal-01243558

D. Vanlandingham, K. Tsetsarkin, C. Hong, K. Klingler, K. Mcelroy et al., Development and characterization of a double subgenomic chikungunya virus infectious clone to express heterologous genes in Aedes aegypti mosqutioes, Insect Biochemistry and Molecular Biology, vol.35, issue.10, pp.1162-1170, 2005.
DOI : 10.1016/j.ibmb.2005.05.008

B. Webster, S. Assil, and M. Dreux, Cell-Cell Sensing of Viral Infection by Plasmacytoid Dendritic Cells, Journal of Virology, vol.90, issue.22, pp.10050-1005301692, 2016.
DOI : 10.1128/JVI.01692-16
URL : http://jvi.asm.org/content/90/22/10050.full.pdf

J. Zhang, A. Raper, N. Sugita, R. Hingorani, M. Salio et al., Characterization of Siglec-H as a novel endocytic receptor expressed on murine plasmacytoid dendritic cell precursors, Blood, vol.107, issue.9, pp.3600-3608, 2006.
DOI : 10.1182/blood-2005-09-3842
URL : http://www.bloodjournal.org/content/bloodjournal/107/9/3600.full.pdf

S. Zhang, B. Saha, K. Kodys, and G. Szabo, IFN-?? production by human natural killer cells in response to HCV-infected hepatoma cells is dependent on accessory cells, Journal of Hepatology, vol.59, issue.3, pp.442-449, 2013.
DOI : 10.1016/j.jhep.2013.04.022
URL : http://europepmc.org/articles/pmc3760030?pdf=render

J. Zhong, P. Gastaminza, G. Cheng, S. Kapadia, T. Kato et al., Robust hepatitis C virus infection in vitro, Proceedings of the National Academy of Sciences, vol.22, issue.8, pp.9294-9299, 2005.
DOI : 10.1016/j.tibtech.2004.06.002