J. Kearney, Innate-like B cells, Springer Seminars in Immunopathology, vol.26, issue.4, pp.377-383, 2005.
DOI : 10.1007/s00281-004-0184-0

E. Montecino-rodriguez and K. Dorshkind, New perspectives in B-1 B cell development and function, Trends in Immunology, vol.27, issue.9, pp.428-433, 2006.
DOI : 10.1016/j.it.2006.07.005

A. Hayday and R. Tigelaar, Regulatory Lymphocytes: Immunoregulation in the tissues by ???? T cells, Nature Reviews Immunology, vol.3, issue.3, pp.233-242, 2003.
DOI : 10.1038/nri1030

A. Bendelac, P. B. Savage, and L. Teyton, The Biology of NKT Cells, Annual Review of Immunology, vol.25, issue.1, pp.297-336, 2007.
DOI : 10.1146/annurev.immunol.25.022106.141711

A. Bendelac, M. Bonneville, and J. Kearney, AUTOREACTIVITY BY DESIGN: INNATE B AND T LYMPHOCYTES, Nature Reviews Immunology, vol.163, issue.3, pp.177-186, 2001.
DOI : 10.1038/35097097

P. Riegert, V. Wanner, and S. Bahram, Genomics, isoforms, expression, and phylogeny of the MHC class I-related MR1 gene, J Immunol, vol.161, pp.4066-4077, 1998.

E. Treiner, Selection of evolutionarily conserved mucosal-associated invariant T cells by MR1, Nature, vol.107, issue.6928, pp.164-169, 2003.
DOI : 10.1126/SCIENCE.1069639

E. Martin, Stepwise Development of MAIT Cells in Mouse and Human, PLoS Biology, vol.1, issue.3, p.54, 2009.
DOI : 10.1371/journal.pbio.1000054.sd001
URL : https://hal.archives-ouvertes.fr/inserm-00707793

F. Tilloy, An Invariant T Cell Receptor ?? Chain Defines a Novel TAP-independent Major Histocompatibility Complex Class Ib???restricted ??/?? T Cell Subpopulation in Mammals, The Journal of Experimental Medicine, vol.156, issue.12, pp.1907-1921, 1999.
DOI : 10.1038/335642a0

I. Kawachi, J. Maldonado, C. Strader, and S. Gilfillan, MR1-Restricted V??19i Mucosal-Associated Invariant T Cells Are Innate T Cells in the Gut Lamina Propria That Provide a Rapid and Diverse Cytokine Response, The Journal of Immunology, vol.176, issue.3, pp.1618-1627, 2006.
DOI : 10.4049/jimmunol.176.3.1618

J. L. Croxford, S. Miyake, Y. Y. Huang, M. Shimamura, and T. Yamamura, Invariant V??19i T cells regulate autoimmune inflammation, Nature Immunology, vol.172, issue.9, pp.987-994, 2006.
DOI : 10.1038/ni1370

S. Santos-sierra, D. T. Golenbock, and P. Henneke, Toll-like receptor-dependent discrimination of streptococci, Journal of Endotoxin Research, vol.115, issue.5, pp.307-312, 2006.
DOI : 10.1177/09680519060120050601

J. Texereau, The Importance of Toll-Like Receptor 2 Polymorphisms in Severe Infections, Clinical Infectious Diseases, vol.41, issue.Supplement 7, pp.408-415, 2005.
DOI : 10.1086/431990

T. Kawai, S. Akira, and . Tlr, TLR signaling, Seminars in Immunology, vol.19, issue.1, pp.24-32, 2007.
DOI : 10.1016/j.smim.2006.12.004

O. Adachi, Targeted Disruption of the MyD88 Gene Results in Loss of IL-1- and IL-18-Mediated Function, Immunity, vol.9, issue.1, pp.143-150, 1998.
DOI : 10.1016/S1074-7613(00)80596-8

F. X. Zhang, Bacterial Lipopolysaccharide Activates Nuclear Factor-??B through Interleukin-1 Signaling Mediators in Cultured Human Dermal Endothelial Cells and Mononuclear Phagocytes, Journal of Biological Chemistry, vol.274, issue.12, pp.7611-7614, 1999.
DOI : 10.1074/jbc.274.12.7611

K. Hoebe, Identification of Lps2 as a key transducer of MyD88-independent TIR signalling, Nature, vol.424, issue.6950, pp.743-748, 2003.
DOI : 10.1038/nature01889

S. E. Girardin, Nod1 Detects a Unique Muropeptide from Gram-Negative Bacterial Peptidoglycan, Science, vol.300, issue.5625, pp.1584-1587, 2003.
DOI : 10.1126/science.1084677

S. E. Girardin, Nod2 Is a General Sensor of Peptidoglycan through Muramyl Dipeptide (MDP) Detection, Journal of Biological Chemistry, vol.278, issue.11, pp.8869-8872, 2003.
DOI : 10.1074/jbc.C200651200

F. Martinon, V. Petrilli, A. Mayor, A. Tardivel, and J. Tschopp, Gout-associated uric acid crystals activate the NALP3 inflammasome, Nature, vol.20, issue.7081, pp.237-241, 2006.
DOI : 10.1038/nature04516

V. Petrilli, Activation of the NALP3 inflammasome is triggered by low intracellular potassium concentration, Cell Death and Differentiation, vol.282, issue.9, pp.1583-1589, 2007.
DOI : 10.1128/MCB.26.3.735-742.2006

S. C. Eisenbarth, O. R. Colegio, W. O-'connor, F. S. Sutterwala, and R. A. Flavell, Crucial role for the Nalp3 inflammasome in the immunostimulatory properties of aluminium adjuvants, Nature, vol.103, issue.7198, pp.1122-1126, 2008.
DOI : 10.1038/nature06939

E. Meylan, Cardif is an adaptor protein in the RIG-I antiviral pathway and is targeted by hepatitis C virus, Nature, vol.69, issue.7062, pp.1167-1172, 2005.
DOI : 10.1016/j.cell.2005.08.012

R. B. Seth, L. Sun, C. K. Ea, and Z. J. Chen, Identification and Characterization of MAVS, a Mitochondrial Antiviral Signaling Protein that Activates NF-??B and IRF3, Cell, vol.122, issue.5, pp.669-682, 2005.
DOI : 10.1016/j.cell.2005.08.012

L. G. Xu, VISA Is an Adapter Protein Required for Virus-Triggered IFN-?? Signaling, Molecular Cell, vol.19, issue.6, pp.727-740, 2005.
DOI : 10.1016/j.molcel.2005.08.014

S. Huang, MR1 antigen presentation to mucosal-associated invariant T cells was highly conserved in evolution, Proceedings of the National Academy of Sciences, vol.106, issue.20, pp.8290-8295, 2009.
DOI : 10.1073/pnas.0903196106

S. Huang, MR1 uses an endocytic pathway to activate mucosal-associated invariant T cells, The Journal of Experimental Medicine, vol.162, issue.5, pp.1201-1211, 2008.
DOI : 10.1016/j.cell.2005.08.018

M. Rottman, Importance of T Cells, Gamma Interferon, and Tumor Necrosis Factor in Immune Control of the Rapid Grower Mycobacterium abscessus in C57BL/6 Mice, Infection and Immunity, vol.75, issue.12, pp.5898-5907, 2007.
DOI : 10.1128/IAI.00014-07

S. K. Mazmanian, C. H. Liu, A. O. Tzianabos, and D. L. Kasper, An Immunomodulatory Molecule of Symbiotic Bacteria Directs Maturation of the Host Immune System, Cell, vol.122, issue.1, pp.107-118, 2005.
DOI : 10.1016/j.cell.2005.05.007

I. Ivanov, Induction of Intestinal Th17 Cells by Segmented Filamentous Bacteria, Cell, vol.139, issue.3, pp.485-498, 2009.
DOI : 10.1016/j.cell.2009.09.033

V. Gaboriau-routhiau, The key role of segmented filamentous bacteria in the coordinated maturation of gut helper T cell responses 32. Shimamura, M. et al. Modulation of Valpha19 NKT cell immune responses by alphamannosyl ceramide derivatives consisting of a series of modified sphingosines, Immunity Eur J Immunol, vol.31, issue.37, pp.677-689, 2007.

J. Schumann, Differential alteration of lipid antigen presentation to NKT cells due to imbalances in lipid metabolism, European Journal of Immunology, vol.70, issue.6, pp.1431-1441, 2007.
DOI : 10.1002/eji.200737160

J. H. Fritz, R. L. Ferrero, D. J. Philpott, and S. E. Girardin, Nod-like proteins in immunity, inflammation and disease, Nature Immunology, vol.176, issue.12, pp.1250-1257, 2006.
DOI : 10.1016/j.cub.2004.10.027

T. Kawai, S. Akira, and . Tlr, TLR signaling, Cell Death and Differentiation, vol.175, issue.5, pp.816-825, 2006.
DOI : 10.1038/nature03124

J. Mattner, Exogenous and endogenous glycolipid antigens activate NKT cells during microbial infections, Nature, vol.172, issue.7032, pp.525-529, 2005.
DOI : 10.1084/jem.184.4.1285

C. Paget, Activation of Invariant NKT Cells by Toll-like Receptor 9-Stimulated Dendritic Cells Requires Type I Interferon and Charged Glycosphingolipids, Immunity, vol.27, issue.4, pp.597-609, 2007.
DOI : 10.1016/j.immuni.2007.08.017
URL : https://hal.archives-ouvertes.fr/hal-00317178

D. Stober, Z. Trobonjaca, J. Reimann, and R. Schirmbeck, Dendritic cells pulsed with exogenous hepatitis B surface antigen particles efficiently present epitopes to MHC class I-restricted cytotoxic T cells, European Journal of Immunology, vol.167, issue.4, pp.1099-1108, 2002.
DOI : 10.1002/1521-4141(200204)32:4<1099::AID-IMMU1099>3.0.CO;2-8

P. H. Gulden, A Listeria monocytogenes Pentapeptide Is Presented to Cytolytic T Lymphocytes by the H2-M3 MHC Class Ib Molecule, Immunity, vol.5, issue.1, pp.73-79, 1996.
DOI : 10.1016/S1074-7613(00)80311-8

L. L. Lenz, B. Dere, and M. J. Bevan, Identification of an H2-M3-Restricted Listeria Epitope: Implications for Antigen Presentation by M3, Immunity, vol.5, issue.1, pp.63-72, 1996.
DOI : 10.1016/S1074-7613(00)80310-6

E. Jouanguy, IL-12 and IFN-?? in host defense against mycobacteria and salmonella in mice and men, Current Opinion in Immunology, vol.11, issue.3, pp.346-351, 1999.
DOI : 10.1016/S0952-7915(99)80055-7

J. H. Fritz, Nod1-Mediated Innate Immune Recognition of Peptidoglycan Contributes to the Onset of Adaptive Immunity, Immunity, vol.26, issue.4, pp.445-459, 2007.
DOI : 10.1016/j.immuni.2007.03.009

T. D. Kanneganti, Critical Role for Cryopyrin/Nalp3 in Activation of Caspase-1 in Response to Viral Infection and Double-stranded RNA, Journal of Biological Chemistry, vol.281, issue.48, pp.36560-36568, 2006.
DOI : 10.1074/jbc.M607594200

S. Paz, Induction of IRF-3 and IRF-7 phosphorylation following activation of the RIG-I pathway, Cell Mol Biol, vol.52, pp.17-28, 2006.

Y. Yao, W. Li, M. H. Kaplan, and C. H. Chang, Interleukin (IL)-4 inhibits IL-10 to promote IL-12 production by dendritic cells, The Journal of Experimental Medicine, vol.160, issue.12, pp.1899-1903, 2005.
DOI : 10.4049/jimmunol.165.1.286