A. Fuchs, W. Vermi, and J. Lee, Intraepithelial Type 1 Innate Lymphoid Cells Are a Unique Subset of IL-12- and IL-15-Responsive IFN-??-Producing Cells, Immunity, vol.38, issue.4, pp.769-81, 2013.
DOI : 10.1016/j.immuni.2013.02.010

J. Schulthess, B. Meresse, and E. Ramiro-puig, Interleukin-15-Dependent NKp46+ Innate Lymphoid Cells Control Intestinal Inflammation by Recruiting Inflammatory Monocytes, Immunity, vol.37, issue.1, pp.108-129, 2012.
DOI : 10.1016/j.immuni.2012.05.013
URL : https://doi.org/10.1016/j.immuni.2012.05.013

A. Michael, C. , L. Brittany, B. Caballero, and S. , Innate immune defenses mediated by two ILC subsets are critical for protection against acute Clostridium difficile infection, Cell Host Microbe, vol.18, pp.27-37, 2015.

S. Dadi, S. Chhangawala, W. Benjamin, and M. , Cancer Immunosurveillance by Tissue-Resident Innate Lymphoid Cells and Innate-like T Cells, Cell, vol.164, issue.3, pp.365-77, 2016.
DOI : 10.1016/j.cell.2016.01.002
URL : https://doi.org/10.1016/j.cell.2016.01.002

F. Vely, V. Barlogis, and B. Vallentin, Evidence of innate lymphoid cell redundancy in humans, Nature Immunology, vol.17, issue.11, pp.1291-1300, 2016.
DOI : 10.3389/fimmu.2012.00344
URL : https://hal.archives-ouvertes.fr/pasteur-01392630

L. Monticelli, G. Sonnenberg, and M. Abt, Innate lymphoid cells promote lung-tissue homeostasis after infection with influenza virus, Nature Immunology, vol.175, issue.11, pp.1045-54, 2011.
DOI : 10.1073/pnas.0506580102

G. Sonnenberg, L. Monticelli, and T. Alenghat, Innate Lymphoid Cells Promote Anatomical Containment of Lymphoid-Resident Commensal Bacteria, Science, vol.7, issue.5, pp.1321-1326, 2012.
DOI : 10.1038/nmeth.f.303

L. Rankin, M. Girard-madoux, and C. Seillet, Complementarity and redundancy of IL-22-producing innate lymphoid cells, Nature Immunology, vol.36, issue.2, pp.179-86, 2016.
DOI : 10.1093/bioinformatics/btp053
URL : https://hal.archives-ouvertes.fr/hal-01440245

C. Song, J. Lee, and S. Gilfillan, ILC3s in models of intestinal inflammation, The Journal of Experimental Medicine, vol.153, issue.11, pp.1869-82, 2015.
DOI : 10.1016/j.immuni.2012.08.026

A. Hanash, J. Dudakov, and G. Hua, Interleukin-22 Protects Intestinal Stem Cells from Immune-Mediated Tissue Damage and Regulates Sensitivity to Graft versus Host Disease, Immunity, vol.37, issue.2, pp.339-50, 2012.
DOI : 10.1016/j.immuni.2012.05.028
URL : https://doi.org/10.1016/j.immuni.2012.05.028

A. Kruglov, S. Grivennikov, and D. Kuprash, Nonredundant Function of Soluble LT??3 Produced by Innate Lymphoid Cells in Intestinal Homeostasis, Science, vol.120, issue.12, pp.1243-1249, 2013.
DOI : 10.1172/JCI43918

M. Hepworth, L. Monticelli, and T. Fung, Innate lymphoid cells regulate CD4+ T-cell responses to intestinal commensal bacteria, Nature, vol.7, issue.7452, pp.113-120, 2013.
DOI : 10.1038/nmeth.f.303
URL : http://europepmc.org/articles/pmc3699860?pdf=render

J. Brestoff, B. Kim, and S. Saenz, Group 2 innate lymphoid cells promote beiging of white adipose tissue and limit obesity, Nature, vol.121, issue.7542, pp.242-248, 2015.
DOI : 10.1172/JCI44271

S. Buonocore, P. Ahern, and H. Uhlig, Innate lymphoid cells drive interleukin-23-dependent innate intestinal pathology, Nature, vol.148, issue.7293, pp.1371-1376, 2010.
DOI : 10.1038/nature08949
URL : http://europepmc.org/articles/pmc3796764?pdf=render

L. Maggi, G. Montaini, and A. Mazzoni, Human circulating group 2 innate lymphoid cells can express CD154 and promote IgE production, Journal of Allergy and Clinical Immunology, vol.139, issue.3, pp.964-76, 2016.
DOI : 10.1016/j.jaci.2016.06.032

N. Rivas, M. Burton, O. Oettgen, H. Chatila, and T. , IL-4 production by group 2 innate lymphoid cells promotes food allergy by blocking regulatory T-cell function, Journal of Allergy and Clinical Immunology, vol.138, issue.3, pp.801-812, 2016.
DOI : 10.1016/j.jaci.2016.02.030

B. Kim, M. Siracusa, and S. Saenz, TSLP Elicits IL-33-Independent Innate Lymphoid Cell Responses to Promote Skin Inflammation, Science Translational Medicine, vol.131, issue.3, pp.170-186, 2013.
DOI : 10.1111/j.1365-2133.1994.tb08530.x

D. Li, R. Guabiraba, and A. Besnard, IL-33 promotes ST2-dependent lung fibrosis by the induction??of alternatively activated macrophages and innate??lymphoid cells in mice, Journal of Allergy and Clinical Immunology, vol.134, issue.6, pp.1422-1454, 2014.
DOI : 10.1016/j.jaci.2014.05.011

R. Duerr, K. Taylor, and S. Brant, A Genome-Wide Association Study Identifies IL23R as an Inflammatory Bowel Disease Gene, Science, vol.314, issue.5804, pp.1461-1464, 2006.
DOI : 10.1126/science.1135245
URL : http://europepmc.org/articles/pmc4410764?pdf=render

A. Geremia, C. Arancibia-cárcamo, and M. Fleming, IL-23???responsive innate lymphoid cells are increased in inflammatory bowel disease, The Journal of Experimental Medicine, vol.208, issue.6, pp.1127-1160, 2011.
DOI : 10.1172/JCI21404
URL : http://jem.rupress.org/content/jem/208/6/1127.full.pdf

H. Kim, H. Lee, and Y. Chang, Interleukin-17???producing innate lymphoid cells and the NLRP3 inflammasome facilitate obesity-associated airway hyperreactivity, Nature Medicine, vol.181, issue.1, pp.54-61, 2014.
DOI : 10.1038/nm851
URL : http://europepmc.org/articles/pmc3912313?pdf=render

F. Villanova, B. Flutter, and I. Tosi, Characterization of Innate Lymphoid Cells in Human Skin and Blood Demonstrates Increase of NKp44+ ILC3 in Psoriasis, Journal of Investigative Dermatology, vol.134, issue.4, pp.984-91, 2014.
DOI : 10.1038/jid.2013.477

C. Picard, J. Casanova, and A. Puel, Infectious Diseases in Patients with IRAK-4, MyD88, NEMO, or I??B?? Deficiency, Clinical Microbiology Reviews, vol.24, issue.3, pp.490-497, 2011.
DOI : 10.1128/CMR.00001-11

T. Bouchery, R. Kyle, and M. Camberis, ILC2s and T cells cooperate to ensure maintenance of M2 macrophages for lung immunity against hookworms, Nature Communications, vol.40, issue.1, p.6970, 2015.
DOI : 10.1021/bi002317h

A. Lim, Y. Li, and S. Lopez-lastra, Systemic Human ILC Precursors Provide a Substrate for Tissue ILC Differentiation, Cell, vol.168, issue.6, pp.1086-100, 2017.
DOI : 10.1016/j.cell.2017.02.021

Y. Simoni, M. Fehlings, and H. Kløverpris, Human Innate Lymphoid Cell Subsets Possess Tissue-Type Based Heterogeneity in Phenotype and Frequency, Immunity, vol.46, issue.1, pp.148-61, 2017.
DOI : 10.1016/j.immuni.2016.11.005

R. 1. Cherrier and M. , Les cellules lympho??des inn??es, m??decine/sciences, vol.30, issue.3, pp.280-288, 2014.
DOI : 10.1051/medsci/20143003012

W. Addison, Experimental and Practical Researches on the Blood: Second Series. Provincial medical journal and retrospect of the medical sciences 1843, pp.444-449

R. Herberman, M. Nunn, H. Holden, and D. Lavrin, Natural cytotoxic reactivity of mouse lymphoid cells against syngeneic and allogeneic tumors. II. Characterization of effector cells, International Journal of Cancer, vol.47, issue.2, pp.230-239, 1975.
DOI : 10.1159/000231208

R. Kiessling, E. Klein, H. Pross, and H. Wigzell, ???Natural??? killer cells in the mouse. II. Cytotoxic cells with specificity for mouse Moloney leukemia cells. Characteristics of the killer cell, European Journal of Immunology, vol.51, issue.2, pp.117-138, 1975.
DOI : 10.1038/newbio244209a0

R. Mebius, P. Rennert, and I. Weissman, Developing Lymph Nodes Collect CD4 + CD3 ??? LT?? + Cells That Can Differentiate to APC, NK Cells, and Follicular Cells but Not T or B Cells, Immunity, vol.7, issue.4, pp.493-504, 1997.
DOI : 10.1016/S1074-7613(00)80371-4
URL : https://doi.org/10.1016/s1074-7613(00)80371-4

M. Cella, A. Fuchs, and W. Vermi, A human natural killer cell subset provides an innate source of IL-22 for mucosal immunity, Nature, vol.3, issue.7230, pp.722-727, 2009.
DOI : 10.4049/jimmunol.172.7.3994

K. Moro, T. Yamada, and M. Tanabe, Innate production of TH2 cytokines by adipose tissue-associated c-Kit+Sca-1+ lymphoid cells, Nature, vol.117, issue.7280, pp.540-544, 2010.
DOI : 10.4049/jimmunol.167.5.2511

E. Narni-mancinelli, J. Chaix, and A. Fenis, Fate mapping analysis of lymphoid cells expressing the NKp46 cell surface receptor, Proceedings of the National Academy of Sciences, vol.201, issue.1, pp.18324-18333, 2011.
DOI : 10.1006/dbio.1998.8971
URL : https://hal.archives-ouvertes.fr/hal-00672199

A. Price, H. Liang, and B. Sullivan, Systemically dispersed innate IL-13-expressing cells in type 2 immunity, Proceedings of the National Academy of Sciences, vol.195, issue.11, pp.11489-94, 2010.
DOI : 10.1084/jem.20020656

N. Satoh-takayama, S. Lesjean-pottier, and P. Vieira, cell subsets from Id2-dependent precursors, The Journal of Experimental Medicine, vol.207, issue.2, pp.273-80, 2010.
DOI : 10.4049/jimmunol.167.5.2511
URL : https://hal.archives-ouvertes.fr/pasteur-00459092

N. Satoh-takayama, C. Vosshenrich, and S. Lesjean-pottier, Microbial Flora Drives Interleukin 22 Production in Intestinal NKp46+ Cells that Provide Innate Mucosal Immune Defense, Immunity, vol.29, issue.6, pp.958-70, 2008.
DOI : 10.1016/j.immuni.2008.11.001
URL : https://hal.archives-ouvertes.fr/pasteur-01402754

C. Vonarbourg, A. Mortha, and V. Bui, Regulated Expression of Nuclear Receptor ROR??t Confers Distinct Functional Fates to NK Cell Receptor-Expressing ROR??t+ Innate Lymphocytes, Immunity, vol.33, issue.5, pp.736-51, 2010.
DOI : 10.1016/j.immuni.2010.10.017

H. Spits, D. Artis, and M. Colonna, Innate lymphoid cells ??? a proposal for uniform nomenclature, Nature Reviews Immunology, vol.37, issue.2, pp.145-154, 2013.
DOI : 10.1016/j.immuni.2012.10.003

V. Cortez, A. Fuchs, and M. Cella, Cutting Edge: Salivary Gland NK Cells Develop Independently of Nfil3 in Steady-State, The Journal of Immunology, vol.192, issue.10, pp.4487-91, 2014.
DOI : 10.4049/jimmunol.1303469

K. Gronke, M. Kofoed-nielsen, and A. Diefenbach, Innate lymphoid cells, precursors and plasticity, Immunology Letters, vol.179, pp.9-18, 2016.
DOI : 10.1016/j.imlet.2016.07.004

G. Belz, ILC2s masquerade as ILC1s to drive chronic disease, Nature Immunology, vol.17, issue.6, pp.611-613, 2016.
DOI : 10.1038/nature11813

J. Bernink, C. Peters, and M. Munneke, Human type 1 innate lymphoid cells accumulate in inflamed mucosal tissues, Nature Immunology, vol.157, issue.3, pp.221-230, 2013.
DOI : 10.1016/j.cell.2007.08.017

Y. Huang, L. Guo, and J. Qiu, IL-25-responsive, lineage-negative KLRG1hi cells are multipotential ???inflammatory??? type 2 innate lymphoid cells, Nature Immunology, vol.785, issue.2, pp.161-170, 2015.
DOI : 10.1126/science.1178334
URL : http://europepmc.org/articles/pmc4297567?pdf=render

N. Crellin, S. Trifari, and C. Kaplan, Regulation of Cytokine Secretion in Human CD127+ LTi-like Innate Lymphoid Cells by Toll-like Receptor 2, Immunity, vol.33, issue.5, pp.752-64, 2010.
DOI : 10.1016/j.immuni.2010.10.012

C. Klose, E. Kiss, and V. Schwierzeck, A T-bet gradient controls the fate and function of CCR6???ROR??t+ innate lymphoid cells, Nature, vol.11, issue.7436, pp.261-266, 2013.
DOI : 10.1038/ni.1825

S. Chea, T. Perchet, and M. Petit, Notch signaling in group 3 innate lymphoid cells modulates their plasticity, Science Signaling, vol.121, issue.426, p.45, 2016.
DOI : 10.1073/pnas.2436557100
URL : https://hal.archives-ouvertes.fr/pasteur-01329903

C. Viant, L. Rankin, and M. Girard-madoux, Transforming growth factor????? and Notch ligands act as opposing environmental cues in regulating the plasticity of type 3 innate lymphoid cells, Science Signaling, vol.9, issue.426, p.46, 2016.
DOI : 10.2202/1544-6115.1027
URL : https://hal.archives-ouvertes.fr/hal-01438546

C. Klose and D. Artis, Innate lymphoid cells as regulators of immunity, inflammation and tissue homeostasis, Nature Immunology, vol.28, issue.7, pp.765-74, 2016.
DOI : 10.1016/j.cell.2014.12.011

E. Zook and B. Kee, Development of innate lymphoid cells, Nature Immunology, vol.38, issue.7, pp.775-82, 2016.
DOI : 10.1016/j.coi.2015.11.005

K. Christoph, S. Flach, M. Möhle, and L. , Differentiation of type 1 ILCs from a common progenitor to all helper-like innate lymphoid cell lineages, Cell, vol.157, pp.340-56, 2014.

M. Constantinides, B. Mcdonald, P. Verhoef, and A. Bendelac, A committed precursor to innate lymphoid cells, Nature, vol.73, issue.7496, pp.397-401, 2014.
DOI : 10.1006/geno.2000.6451

C. Seillet, L. Mielke, and D. Amann-zalcenstein, Deciphering the Innate Lymphoid Cell Transcriptional Program, Cell Reports, vol.17, issue.2, pp.436-483, 2016.
DOI : 10.1016/j.celrep.2016.09.025

G. Gasteiger, X. Fan, and S. Dikiy, Tissue residency of innate lymphoid cells in lymphoid and nonlymphoid organs, Science, vol.102, issue.4, pp.981-986, 2015.
DOI : 10.1182/blood-2003-01-0318

M. Gury-benari, C. Thaiss, and N. Serafini, The Spectrum and Regulatory Landscape of Intestinal Innate Lymphoid Cells Are Shaped by the Microbiome, Cell, vol.166, issue.5, pp.1231-1277, 2016.
DOI : 10.1016/j.cell.2016.07.043

C. Vosshenrich, T. Ranson, and S. Samson, Roles for Common Cytokine Receptor ??-Chain-Dependent Cytokines in the Generation, Differentiation, and Maturation of NK Cell Precursors and Peripheral NK Cells in Vivo, The Journal of Immunology, vol.174, issue.3, pp.1213-1234, 2005.
DOI : 10.4049/jimmunol.174.3.1213

E. Montaldo, L. Teixeira-alves, and T. Glatzer, Human ROR??t+CD34+ Cells Are Lineage-Specified Progenitors of Group 3 ROR??t+ Innate Lymphoid Cells, Immunity, vol.41, issue.6, pp.988-1000, 2014.
DOI : 10.1016/j.immuni.2014.11.010

J. Ettersperger, N. Montcuquet, and G. Malamut, Interleukin-15-Dependent T-Cell-like Innate Intraepithelial Lymphocytes Develop in the Intestine and Transform into Lymphomas in Celiac Disease, Immunity, vol.45, issue.3, pp.610-635, 2016.
DOI : 10.1016/j.immuni.2016.07.018