T. P. Monie, M. C. Moncrieffe, and N. J. Gay, Structure and regulation of cytoplasmic adapter proteins involved in innate immune signaling, Immunological Reviews, vol.30, issue.1, pp.161-175, 2009.
DOI : 10.1111/j.1600-065X.2008.00735.x

L. Franchi, R. Munoz-planillo, and G. Nunez, Sensing and reacting to microbes through the inflammasomes, Nature Immunology, vol.180, issue.4, pp.325-332, 2012.
DOI : 10.1038/nature07725

N. B. Bryan, A. Dorfleutner, Y. Rojanasakul, and C. Stehlik, Activation of Inflammasomes Requires Intracellular Redistribution of the Apoptotic Speck-Like Protein Containing a Caspase Recruitment Domain, The Journal of Immunology, vol.182, issue.5, pp.3173-3182, 2009.
DOI : 10.4049/jimmunol.0802367

A. Lu, Unified Polymerization Mechanism for the Assembly of ASC-Dependent Inflammasomes, Cell, vol.156, issue.6, pp.1193-1206, 2014.
DOI : 10.1016/j.cell.2014.02.008

T. Fernandes-alnemri, The pyroptosome: a supramolecular assembly of ASC dimers mediating inflammatory cell death via caspase-1 activation, Cell Death and Differentiation, vol.78, issue.9, pp.1590-1604, 2007.
DOI : 10.1016/j.cell.2004.05.004

A. Stutz, G. L. Horvath, B. G. Monks, and E. Latz, ASC Speck Formation as a Readout for Inflammasome Activation, Methods in molecular biology, vol.1040, pp.91-101, 2013.
DOI : 10.1007/978-1-62703-523-1_8

S. Mariathasan, Differential activation of the inflammasome by caspase-1 adaptors ASC and Ipaf, Nature, vol.20, issue.6996, pp.213-218, 2004.
DOI : 10.1074/jbc.C300460200

B. S. Franklin, The adaptor ASC has extracellular and 'prionoid' activities that propagate inflammation, Nature Immunology, vol.442, issue.8, pp.727-737, 2014.
DOI : 10.1016/j.cell.2012.07.021

A. Baroja-mazo, The NLRP3 inflammasome is released as a particulate danger signal that amplifies the inflammatory response, Nature Immunology, vol.442, issue.8, pp.738-748, 2014.
DOI : 10.1126/science.7535475

V. Compan, A genetically encoded IL-1beta bioluminescence resonance energy transfer sensor to monitor inflammasome activity 11. Compan, V., et al. Cell volume regulation modulates NLRP3 inflammasome activation, J Immunol Immunity, vol.189, issue.37, pp.2131-2137, 2012.

M. Kindermann, Selective and Sensitive Monitoring of Caspase-1 Activity by a Novel Bioluminescent Activity-Based Probe, Chemistry & Biology, vol.17, issue.9, pp.999-1007, 2010.
DOI : 10.1016/j.chembiol.2010.07.011

E. Bartok, iGLuc: a luciferase-based inflammasome and protease activity reporter, Nature Methods, vol.4, issue.2, pp.147-154, 2013.
DOI : 10.1038/nmeth.2327

C. A. Dinarello, Immunological and Inflammatory Functions of the Interleukin-1 Family, Annual Review of Immunology, vol.27, issue.1, pp.519-550, 2009.
DOI : 10.1146/annurev.immunol.021908.132612

P. Rider, IL-1?? and IL-1?? Recruit Different Myeloid Cells and Promote Different Stages of Sterile Inflammation, The Journal of Immunology, vol.187, issue.9, pp.4835-4843, 2011.
DOI : 10.4049/jimmunol.1102048

W. Kastenmuller, P. Torabi-parizi, N. Subramanian, T. Lammermann, and R. N. Germain, A Spatially-Organized Multicellular Innate Immune Response in Lymph Nodes Limits Systemic Pathogen Spread, Cell, vol.150, issue.6, pp.1235-1248, 2012.
DOI : 10.1016/j.cell.2012.07.021

S. J. Rowe, L. Allen, V. C. Ridger, P. G. Hellewell, and M. K. Whyte, Caspase-1-Deficient Mice Have Delayed Neutrophil Apoptosis and a Prolonged Inflammatory Response to Lipopolysaccharide-Induced Acute Lung Injury, The Journal of Immunology, vol.169, issue.11, pp.6401-6407, 2002.
DOI : 10.4049/jimmunol.169.11.6401

O. Gross, Syk kinase signalling couples to the Nlrp3 inflammasome for anti-fungal host defence, Nature, vol.11, issue.7245, pp.433-436, 2009.
DOI : 10.1038/nature07965

T. Ichinohe, H. K. Lee, Y. Ogura, R. Flavell, and A. Iwasaki, Inflammasome recognition of influenza virus is essential for adaptive immune responses, The Journal of Experimental Medicine, vol.163, issue.1, pp.79-87, 2009.
DOI : 10.1126/science.1087262

M. T. Shio, Correction: Malarial Hemozoin Activates the NLRP3 Inflammasome through Lyn and Syk Kinases, PLoS Pathogens, vol.5, issue.9, p.1000559, 2009.
DOI : 10.1371/annotation/abca067d-b82b-4de6-93c5-0fcc38e3df05

D. S. Lima-junior, Inflammasome-derived IL-1?? production induces nitric oxide???mediated resistance to Leishmania, Nature Medicine, vol.70, issue.7, pp.909-915, 2013.
DOI : 10.1126/science.6451927

F. Ghiringhelli, Activation of the NLRP3 inflammasome in dendritic cells induces IL-1?????dependent adaptive immunity against tumors, Nature Medicine, vol.7, issue.10, pp.1170-1178, 2009.
DOI : 10.1038/nm.2028
URL : https://hal.archives-ouvertes.fr/hal-00419823

Y. Chung, Critical Regulation of Early Th17 Cell Differentiation by Interleukin-1 Signaling, Immunity, vol.30, issue.4, pp.576-587, 2009.
DOI : 10.1016/j.immuni.2009.02.007

S. Z. Ben-sasson, IL-1 enhances expansion, effector function, tissue localization, and memory response of antigen-specific CD8 T cells, The Journal of Experimental Medicine, vol.160, issue.3, pp.491-502, 2013.
DOI : 10.1172/JCI39293

J. Delaloye, Innate Immune Sensing of Modified Vaccinia Virus Ankara (MVA) Is Mediated by TLR2-TLR6, MDA-5 and the NALP3 Inflammasome, PLoS Pathogens, vol.387, issue.6, p.1000480, 2009.
DOI : 10.1371/journal.ppat.1000480.s007

Z. Waibler, Modified Vaccinia Virus Ankara Induces Toll-Like Receptor-Independent Type I Interferon Responses, Journal of Virology, vol.81, issue.22, pp.12102-12110, 2007.
DOI : 10.1128/JVI.01190-07

V. Hornung, AIM2 recognizes cytosolic dsDNA and forms a caspase-1-activating inflammasome with ASC, Nature, vol.326, issue.7237, pp.514-518, 2009.
DOI : 10.1038/nature07725

O. Gross, C. J. Thomas, G. Guarda, and J. Tschopp, The inflammasome: an integrated view, Immunological Reviews, vol.126, issue.Suppl, pp.136-151, 2011.
DOI : 10.1111/j.1600-065X.2011.01046.x

O. Gross, Measuring the Inflammasome, Methods in molecular biology, vol.844, pp.199-222, 2012.
DOI : 10.1007/978-1-61779-527-5_15

A. Iwasaki, A virological view of innate immune recognition. Annual review of microbiology 66, pp.177-196, 2012.

T. Junt, Subcapsular sinus macrophages in lymph nodes clear lymph-borne viruses and present them to antiviral B cells, Nature, vol.9, issue.7166, pp.110-114, 2007.
DOI : 10.1038/nature06287

W. Kastenmuller, Peripheral Prepositioning and Local CXCL9 Chemokine-Mediated Guidance Orchestrate Rapid Memory CD8+ T Cell Responses in the Lymph Node, Immunity, vol.38, issue.3, pp.502-513, 2013.
DOI : 10.1016/j.immuni.2012.11.012

Z. Garcia, Subcapsular sinus macrophages promote NK cell accumulation and activation in response to lymph-borne viral particles, Blood, vol.120, issue.24, pp.4744-4750, 2012.
DOI : 10.1182/blood-2012-02-408179
URL : https://hal.archives-ouvertes.fr/pasteur-01110078

B. Balci-peynircioglu, Expression of ASC in Renal Tissues of Familial Mediterranean Fever Patients with Amyloidosis: Postulating a Role for ASC in AA Type Amyloid Deposition, Experimental Biology and Medicine, vol.233, issue.11, pp.1324-1333, 2008.
DOI : 10.3181/0803-RM-106

T. G. Phan, J. A. Green, E. E. Gray, Y. Xu, and J. G. Cyster, Immune complex relay by subcapsular sinus macrophages and noncognate B cells drives antibody affinity maturation, Nature Immunology, vol.3, issue.7, pp.786-793, 2009.
DOI : 10.1038/ni.1745

E. A. Miao, J. V. Rajan, and A. Aderem, Caspase-1-induced pyroptotic cell death, Immunological Reviews, vol.12, issue.1, pp.206-214, 2011.
DOI : 10.1111/j.1600-065X.2011.01044.x

T. Fernandes-alnemri and E. S. Alnemri, Chapter Thirteen Assembly, Purification, and Assay of the Activity of the ASC Pyroptosome, Methods in enzymology, vol.442, pp.251-270, 2008.
DOI : 10.1016/S0076-6879(08)01413-4

M. H. Lehmann, Modified Vaccinia Virus Ankara Triggers Chemotaxis of Monocytes and Early Respiratory Immigration of Leukocytes by Induction of CCL2 Expression, Journal of Virology, vol.83, issue.6, pp.2540-2552, 2009.
DOI : 10.1128/JVI.01884-08

G. Dvoriantchikova, Genetic Ablation of Pannexin1 Protects Retinal Neurons from Ischemic Injury, PLoS ONE, vol.76, issue.2, p.31991, 2012.
DOI : 10.1371/journal.pone.0031991.s011

E. Mezzaroma, The inflammasome promotes adverse cardiac remodeling following acute myocardial infarction in the mouse, Proceedings of the National Academy of Sciences, vol.108, issue.49, pp.19725-19730, 2011.
DOI : 10.1073/pnas.1108586108

H. B. Tran, Immunolocalization of NLRP3 Inflammasome in Normal Murine Airway Epithelium and Changes following Induction of Ovalbumin-Induced Airway Inflammation, Journal of Allergy, vol.174, issue.11, p.819176, 2012.
DOI : 10.1111/j.1398-9995.2011.02586.x

Y. Shirasaki, Real-time single-cell imaging of protein secretion, Scientific Reports, vol.140, p.4736, 2014.
DOI : 10.1038/srep04736

T. Liu, Single-Cell Imaging of Caspase-1 Dynamics Reveals an All-or-None Inflammasome Signaling Response, Cell Reports, vol.8, issue.4, pp.974-982, 2014.
DOI : 10.1016/j.celrep.2014.07.012

J. S. Cho, Neutrophil-derived IL-1?? Is Sufficient for Abscess Formation in Immunity against Staphylococcus aureus in Mice, PLoS Pathogens, vol.209, issue.11, p.1003047, 2012.
DOI : 10.1371/journal.ppat.1003047.s017

S. U. Seo, Distinct Commensals Induce Interleukin-1?? via NLRP3 Inflammasome in Inflammatory Monocytes to Promote Intestinal Inflammation in Response to Injury, Immunity, vol.42, issue.4, pp.744-755, 2015.
DOI : 10.1016/j.immuni.2015.03.004

T. Chtanova, Dynamics of Neutrophil Migration in Lymph Nodes during Infection, Immunity, vol.29, issue.3, pp.487-496, 2008.
DOI : 10.1016/j.immuni.2008.07.012

M. Gaya, Inflammation-induced disruption of SCS macrophages impairs B cell responses to secondary infection, Science, vol.347, issue.6222, pp.667-672, 2015.
DOI : 10.1126/science.aaa1300

T. Lammermann, Neutrophil swarms require LTB4 and integrins at sites of cell death in vivo, Nature, vol.206, issue.7454, pp.371-375, 2013.
DOI : 10.1038/nature12175

B. Mcdonald, Intravascular Danger Signals Guide Neutrophils to Sites of Sterile Inflammation, Science, vol.330, issue.6002, pp.362-366, 2010.
DOI : 10.1126/science.1195491

M. T. Lotze, The grateful dead: damage-associated molecular pattern molecules and reduction/oxidation regulate immunity, Immunological Reviews, vol.28, issue.1, pp.60-81, 2007.
DOI : 10.1007/s00109-005-0688-7

Q. Zhang, Circulating mitochondrial DAMPs cause inflammatory responses to injury, Nature, vol.24, issue.7285, pp.104-107, 2010.
DOI : 10.1038/nature08780

F. A. Amaral, NLRP3 inflammasome-mediated neutrophil recruitment and hypernociception depend on leukotriene B4 in a murine model of gout, Arthritis & Rheumatism, vol.97, issue.2, pp.474-484, 2012.
DOI : 10.1002/art.33355

V. Kumar, Global lymphoid tissue remodeling during a viral infection is orchestrated by a B cell-lymphotoxin-dependent pathway, Blood, vol.115, issue.23, pp.4725-4733, 2010.
DOI : 10.1182/blood-2009-10-250118

C. Dostert, K. Ludigs, and G. Guarda, Innate and adaptive effects of inflammasomes on T cell responses, Current Opinion in Immunology, vol.25, issue.3, pp.359-365, 2013.
DOI : 10.1016/j.coi.2013.02.008

V. Dixit, Nlrp3 Inflammasome Activation in Type 2 Diabetes: Is It Clinically Relevant?, Diabetes, vol.62, issue.1, pp.22-24, 2013.
DOI : 10.2337/db12-1115

M. Yang, C. H. Hearnden, E. Oleszycka, and E. C. Lavelle, NLRP3 Inflammasome Activation and Cytotoxicity Induced by Particulate Adjuvants, Methods in molecular biology, vol.1040, pp.41-63, 2013.
DOI : 10.1007/978-1-62703-523-1_5

O. Donnell and H. , Toll-like Receptor and Inflammasome Signals Converge to Amplify the Innate Bactericidal Capacity of T Helper 1 Cells, Immunity, vol.40, issue.2, pp.213-224, 2014.
DOI : 10.1016/j.immuni.2013.12.013

A. Dunne, Inflammasome Activation by Adenylate Cyclase Toxin Directs Th17 Responses and Protection against Bordetella pertussis, The Journal of Immunology, vol.185, issue.3, pp.1711-1719, 2010.
DOI : 10.4049/jimmunol.1000105

S. Z. Ben-sasson, IL-1 acts directly on CD4 T cells to enhance their antigen-driven expansion and differentiation, Proceedings of the National Academy of Sciences, vol.106, issue.17, pp.7119-7124, 2009.
DOI : 10.1073/pnas.0902745106

S. Brandler, Preclinical Studies of a Modified Vaccinia Virus Ankara-Based HIV Candidate Vaccine: Antigen Presentation and Antiviral Effect, Journal of Virology, vol.84, issue.10, pp.5314-5328, 2010.
DOI : 10.1128/JVI.02329-09
URL : https://hal.archives-ouvertes.fr/pasteur-00488573

A. Stutz, G. L. Horvath, B. G. Monks, and E. Latz, ASC Speck Formation as a Readout for Inflammasome Activation, Methods in molecular biology, vol.1040, pp.91-101, 2013.
DOI : 10.1007/978-1-62703-523-1_8

T. Nakano, H. Kodama, and T. Honjo, Generation of lymphohematopoietic cells from embryonic stem cells in culture, Science, vol.265, issue.5175, pp.1098-1101, 1994.
DOI : 10.1126/science.8066449

Z. Garcia, Subcapsular sinus macrophages promote NK cell accumulation and activation in response to lymph-borne viral particles, Blood, vol.120, issue.24, pp.4744-4750, 2012.
DOI : 10.1182/blood-2012-02-408179
URL : https://hal.archives-ouvertes.fr/pasteur-01110078

S. Celli, B. Breart, and P. Bousso, Intravital Two-Photon Imaging of Natural Killer Cells and Dendritic Cells in Lymph Nodes, Methods Mol Biol, vol.415, pp.119-126, 2008.
DOI : 10.1007/978-1-59745-570-1_7