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Adaptation of Innate Lymphoid Cells to a Micronutrient Deficiency Promotes Type 2 Barrier Immunity
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How the immune system adapts to malnutrition to sustain immunity at barrier surfaces, such as the intestine, remains unclear. Vitamin A deficiency is one of the most common micronutrient deficiencies and is associated with profound defects in adaptive immunity. Here, we found that type 3 innate lymphoid cells (ILC3s) are severely diminished in vitamin A–deficient settings, which results in compromised immunity to acute bacterial infection. However, vitamin A deprivation paradoxically resulted in dramatic expansion of interleukin-13 (IL-13)–producing ILC2s and resistance to nematode infection in mice, which revealed that ILCs are primary sensors of dietary stress. Further, these data indicate that, during malnutrition, a switch to innate type 2 immunity may represent a powerful adaptation of the immune system to promote host survival in the face of ongoing barrier challenges.
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“the depletion of vitamin A, in the adult, led to a decrease of Th1, Th17, and ILC3 responses (a synonym of lowered immunity to bacterial infection), an effect which is counteracted through time127.”
From Advances and challenges in retinoid delivery systems in regenerative and therapeutic medicine (2020) · cites this paper as [127]
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Cites
Ecological and Evolutionary Forces Shaping Microbial Diversity in the Human Intestine
Ley, R. E., Peterson, D. A., & Gordon, J. I. (2006) · Cell · doi:10.1016/j.cell.2006.02.017 · Cited by 3,358
Innate lymphoid cells — a proposal for uniform nomenclature
Spits, H., Artis, D., Colonna, M., Diefenbach, A., Disanto, J. D., Eberl, G., Koyasu, S., Locksley, R., McKenzie, A., Mebius, R., et al. (2013) · Nature reviews. Immunology · doi:10.1038/nri3365 · Cited by 2,380
Sun, C., Hall, J. A., Blank, R. B., Bouladoux, N. J., Oukka, M., Mora, J. R., & Belkaid, Y. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20070602 · Cited by 1,880
Self-citationMucin dynamics and enteric pathogens
McGuckin, M. A., Lindén, S. K., Sutton, P., & Florin, T. H. (2011) · Nature Reviews Microbiology · doi:10.1038/nrmicro2538 · Cited by 1,428
Malnutrition and Infection: Complex Mechanisms and Global Impacts
Schaible, U. E., & Kaufmann, S. H. E. (2007) · PLoS Medicine · doi:10.1371/journal.pmed.0040115 · Cited by 991
Wynn, T. A. (2003) · Annual Review of Immunology · doi:10.1146/annurev.immunol.21.120601.141142 · Cited by 991
Self-citationThe Aryl Hydrocarbon Receptor Regulates Gut Immunity through Modulation of Innate Lymphoid Cells
Qiu, J., Heller, J. J., Guo, X., Chen, Z. E., Fish, K., Fu, Y., & Zhou, L. (2011) · Immunity · doi:10.1016/j.immuni.2011.11.011 · Cited by 889
The Transcription Factor GATA-3 Controls Cell Fate and Maintenance of Type 2 Innate Lymphoid Cells
Hoyler, T., Klose, C. S. N., Souabni, A., Turqueti‐Neves, A., Pfeifer, D., Rawlins, E. L., Voehringer, D., Busslinger, M., & Diefenbach, A. (2012) · Immunity · doi:10.1016/j.immuni.2012.06.020 · Cited by 873
Spits, H., & Santo, J. P. D. (2010) · Nature Immunology · doi:10.1038/ni.1962 · Cited by 840
Exogenous Stimuli Maintain Intraepithelial Lymphocytes via Aryl Hydrocarbon Receptor Activation
Li, Y., Innocentin, S., Withers, D. R., Roberts, N. A., Gallagher, A., Grigorieva, E. F., Wilhelm, C., & Veldhoen, M. (2011) · Cell · doi:10.1016/j.cell.2011.09.025 · Cited by 837
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Th2 and Th1 Responses: Clear and Hidden Sides of Immunity Against Intestinal Helminths
Cortés, A., Muñoz-Antolí, C., Esteban, J. G., & Toledo, R. (2017) · Trends in Parasitology · doi:10.1016/j.pt.2017.05.004 · Cited by 108
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Kónya, V., Czarnewski, P., Forkel, M., Rao, A., Kokkinou, E., Villablanca, E. J., Almer, S. H., Lindforss, U., Friberg, D., Höög, C., et al. (2017) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2017.01.045 · Cited by 99
Group 3 Innate Lymphoid Cells: Communications Hubs of the Intestinal Immune System
Withers, D. R., & Hepworth, M. R. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01298 · Cited by 97
Immune dysregulation in the functional gastrointestinal disorders
Keely, S., Walker, M. M., Marks, E., & Talley, N. J. (2015) · European Journal of Clinical Investigation · doi:10.1111/eci.12548 · Cited by 96
Retinoic Acid and Its Role in Modulating Intestinal Innate Immunity
Czarnewski, P., Das, S., Parigi, S. M., & Villablanca, E. J. (2017) · Nutrients · doi:10.3390/nu9010068 · Cited by 99
The unusual suspects—innate lymphoid cells as novel therapeutic targets in IBD
Goldberg, R., Prescott, N. J., Lord, G. M., MacDonald, T. T., & Powell, N. (2015) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2015.52 · Cited by 94
IL-33–Responsive Group 2 Innate Lymphoid Cells Are Regulated by Female Sex Hormones in the Uterus
Bartemes, K. R., Chen, C.-C., Iijima, K., Drake, L. Y., & Kita, H. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1602085 · Cited by 93
Innate lymphoid cells in intestinal immunity and inflammation
Bostick, J. W., & Zhou, L. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-2055-3 · Cited by 92
Bando, J. K., Gilfillan, S., Song, C., McDonald, K. G., Huang, S. C., Newberry, R. D., Kobayashi, Y., Allan, D., Carlyle, J. R., Cella, M., et al. (2018) · Immunity · doi:10.1016/j.immuni.2018.04.012 · Cited by 92
IL-22BP is produced by eosinophils in human gut and blocks IL-22 protective actions during colitis
Martin, J. P. D., Bériou, G., Heslan, M., Bossard, C., Jarry, A., Abidi, A., Hulin, P., Ménoret, S., Thinard, R., Anegón, I., et al. (2015) · Mucosal Immunology · doi:10.1038/mi.2015.83 · Cited by 92
Kim, S., Cho, B.-H., Kiyono, H., & Jang, Y. (2017) · Scientific Reports · doi:10.1038/s41598-017-02729-6 · Cited by 97
Ganal-Vonarburg, S. C., & Duerr, C. U. (2019) · Immunology · doi:10.1111/imm.13138 · Cited by 91
Breast Milk and Solid Food Shaping Intestinal Immunity
Parigi, S. M., Eldh, M., Larssen, P., Gabrielsson, S., & Villablanca, E. J. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00415 · Cited by 97
Distribution and storage of inflammatory memory in barrier tissues
Ordovás-Montañés, J., Beyaz, S., Rakoff-Nahoum, S., & Shalek, A. K. (2020) · Nature reviews. Immunology · doi:10.1038/s41577-019-0263-z · Cited by 94
Nutrition Regulates Innate Immunity in Health and Disease
Nobs, S. P., Zmora, N., & Elinav, E. (2020) · Annual Review of Nutrition · doi:10.1146/annurev-nutr-120919-094440 · Cited by 93
The pleiotropic role of vitamin A in regulating mucosal immunity.
Sirisinha, S. (2015) · PubMed · Cited by 87
The Multi-Modal Immune Pathogenesis of Atopic Eczema
Eyerich, K., Eyerich, S., & Biedermann, T. (2015) · Trends in Immunology · doi:10.1016/j.it.2015.10.006 · Cited by 90
Transcriptional and epigenetic networks of helper T and innate lymphoid cells
Shih, H., Sciumè, G., Poholek, A. C., Vahedi, G., Hirahara, K., Villarino, A. V., Bonelli, M. M., Bosselut, R., Kanno, Y., Muljo, S. A., et al. (2014) · Immunological Reviews · doi:10.1111/imr.12208 · Cited by 91
Allergic diseases: From bench to clinic - Contribution of the discovery of interleukin-5
Yanagibashi, T., Satoh, M., Nagai, Y., Koike, M., & Takatsu, K. (2017) · Cytokine · doi:10.1016/j.cyto.2016.11.011 · Cited by 93
Cytokine Networks between Innate Lymphoid Cells and Myeloid Cells
Mortha, A., & Burrows, K. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00191 · Cited by 88
Activation and Suppression of Group 3 Innate Lymphoid Cells in the Gut
Zhou, W., & Sonnenberg, G. F. (2020) · Trends in Immunology · doi:10.1016/j.it.2020.06.009 · Cited by 86
Mucosal Immune Development in Early Life: Setting the Stage
Brugman, S., Perdijk, O., van Neerven, R. J. J., & Savelkoul, H. F. J. (2015) · Archivum Immunologiae et Therapiae Experimentalis · doi:10.1007/s00005-015-0329-y · Cited by 88
Differentiation of human innate lymphoid cells (ILCs)
Juelke, K., & Romagnani, C. (2015) · Current Opinion in Immunology · doi:10.1016/j.coi.2015.11.005 · Cited by 92
Group 2 innate lymphoid cells in disease
Halim, T. Y. F. (2015) · International Immunology · doi:10.1093/intimm/dxv050 · Cited by 81
Innate lymphoid cells in secondary lymphoid organs
Bar‐Ephraïm, Y. E., & Mebius, R. E. (2016) · Immunological Reviews · doi:10.1111/imr.12407 · Cited by 81
Goverse, G., Labão‐Almeida, C., Ferreira, M., Molenaar, R., Wahlen, S., Konijn, T., Koning, J. J., Veiga‐Fernandes, H., & Mebius, R. E. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1501106 · Cited by 82
Yu, H. B., Yang, H., Allaire, J. M., Ma, C., Graef, F. A., Mortha, A., Liang, Q., Bosman, E. S., Reid, G. S. D., Waschek, J. A., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2106634118 · Cited by 79
Eosinophil-Derived IL-10 Supports Chronic Nematode Infection
Huang, L., Gebreselassie, N. G., Gagliardo, L. F., Ruyechan, M. C., Lee, N. A., Lee, J. J., & Appleton, J. A. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1400852 · Cited by 80
Rizzetto, L., Filippo, C. D., & Cavalieri, D. (2014) · European Journal of Immunology · doi:10.1002/eji.201344403 · Cited by 79
Rosa, V. D., Galgani, M., Santopaolo, M., Colamatteo, A., Laccetti, R., & Matarese, G. (2015) · Seminars in Immunology · doi:10.1016/j.smim.2015.10.001 · Cited by 77
Gut Commensals Expand Vitamin A Metabolic Capacity of the Mammalian Host
Bonakdar, M., Czuba, L. C., Han, G., Zhong, G. G., Luong, H. T., Isoherranen, N., & Vaishnava, S. (2022) · Cell Host & Microbe · doi:10.1016/j.chom.2022.06.011 · Cited by 76
Group 3 innate lymphoid cells in intestinal health and disease
Horn, V., & Sonnenberg, G. F. (2024) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-024-00906-3 · Cited by 80
Vacchio, M. S., Wang, L., Bouladoux, N. J., Carpenter, A. C., Xiong, Y., Williams, L., Wohlfert, E. A., Song, K., Belkaid, Y., Love, P. E., et al. (2014) · Nature Immunology · doi:10.1038/ni.2960 · Cited by 72
Self-citationCurrent Understanding of Innate Immune Cell Dysfunction in Childhood Undernutrition
Bourke, C. D., Jones, K. D. J., & Prendergast, A. J. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01728 · Cited by 72
Gpr109a Limits Microbiota-Induced IL-23 Production To Constrain ILC3-Mediated Colonic Inflammation
Bhatt, B., Zeng, P., Zhu, H., Sivaprakasam, S., Li, S., Xiao, H., Dong, L., Shiao, S.-Y. P. K., Kolhe, R. B., Patel, N., et al. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1701625 · Cited by 71
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von Burg, N., Turchinovich, G., & Finke, D. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00416 · Cited by 69
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Cong, J. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01989 · Cited by 73
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Fu, T., Li, Y., Oh, T. G., Cayabyab, F., He, N., Tang, Q., Coulter, S., Truitt, M., Medina, P., He, M., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2213041119 · Cited by 68
Ruiter, B., Patil, S. U., & Shreffler, W. G. (2015) · Clinical & Experimental Allergy · doi:10.1111/cea.12568 · Cited by 68
Innate immunity in the lung regulates the development of asthma
DeKruyff, R. H., Yu, S., Kim, H. Y., & Umetsu, D. T. (2014) · Immunological Reviews · doi:10.1111/imr.12187 · Cited by 69
Group 2 Innate Lymphoid Cells in the Regulation of Immune Responses
Roediger, B., & Weninger, W. (2014) · Advances in immunology · doi:10.1016/bs.ai.2014.09.004 · Cited by 70
Yamaguchi, T., Takizawa, F., Fischer, U., & Dijkstra, J. M. (2015) · Biology · doi:10.3390/biology4040814 · Cited by 67
Domingues, R. G., & Hepworth, M. R. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00116 · Cited by 73
Interplay of innate lymphoid cells and the microbiota
Britanova, L. V., & Diefenbach, A. (2017) · Immunological Reviews · doi:10.1111/imr.12580 · Cited by 63
Metabolic Control of Innate Lymphoid Cell Migration
Willinger, T. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02010 · Cited by 65
Development and regulation of RORγt+ innate lymphoid cells
Cording, S., Medvedovic, J., Cherrier, M., & Eberl, G. (2014) · FEBS Letters · doi:10.1016/j.febslet.2014.03.034 · Cited by 65
The Innate Lymphoid Cell Precursor
Ishizuka, I. E., Constantinides, M. G., Gudjonson, H., & Bendelac, A. S. (2016) · Annual Review of Immunology · doi:10.1146/annurev-immunol-041015-055549 · Cited by 68
Jijon, H. B., Suárez-López, L., Diaz, O. E., Das, S., Calisto, J. D., Yaffe, M. B., Pittet, M. J., Mora, J. R., Belkaid, Y., Xavier, R. J., et al. (2017) · Mucosal Immunology · doi:10.1038/mi.2017.91 · Cited by 65
Self-citationThe role of innate lymphoid cells in response to microbes at mucosal surfaces
Seo, G., Giles, D. A., & Kronenberg, M. (2020) · Mucosal Immunology · doi:10.1038/s41385-020-0265-y · Cited by 61
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Cella, M., Miller, H. L., & Song, C. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00282 · Cited by 61
Parasites, nutrition, immune responses and biology of metabolic tissues
Shea‐Donohue, T., Qin, B., & Smith, A. D. (2017) · Parasite Immunology · doi:10.1111/pim.12422 · Cited by 62
Interactions between the microbiota and innate and innate-like lymphocytes
Constantinides, M. G. (2017) · Journal of Leukocyte Biology · doi:10.1002/jlb.3ri0917-378r · Cited by 56
Bayha, K. M., Ortell, N., Ryan, C. N., Griffitt, K. J., Krasnec, M. O., Sena, J. A., Ramaraj, T., Takeshita, R., Mayer, G. D., Schilkey, F., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0176559 · Cited by 56
The balance of power: innate lymphoid cells in tissue inflammation and repair
Castellanos, J. G., & Longman, R. (2019) · Journal of Clinical Investigation · doi:10.1172/jci124617 · Cited by 57
Type 2 innate lymphoid cells in the induction and resolution of tissue inflammation
Wallrapp, A., Riesenfeld, S. J., Burkett, P. R., & Kuchroo, V. K. (2018) · Immunological Reviews · doi:10.1111/imr.12702 · Cited by 57
Proline uptake promotes activation of lymphoid tissue inducer cells to maintain gut homeostasis
Wu, D., Li, Z., Zhang, Y., Zhang, Y., Ren, G., Zeng, Y., Liu, H., Guan, W., Zhao, X., Li, P., et al. (2023) · Nature Metabolism · doi:10.1038/s42255-023-00908-6 · Cited by 54
Potential mechanisms regulating pulmonary pathology in inflammatory bowel disease
Mateer, S. W., Maltby, S., Marks, E., Foster, P. S., Horvat, J. C., Hansbro, P. M., & Keely, S. (2015) · Journal of Leukocyte Biology · doi:10.1189/jlb.3ru1114-563r · Cited by 56
Critical role of IL22/IL22RA1 signaling in pneumococcal pneumonia
Trevejo-Nuñez, G., Elsegeiny, W., Conboy, P., Chen, K., & Kolls, J. (2016) · Journal of Immunology · doi:10.4049/jimmunol.1600528 · Cited by 52
A Proinflammatory Role of Type 2 Innate Lymphoid Cells in Murine Immune-Mediated Hepatitis
Neumann, K., Karimi, K., Meiners, J., Voetlause, R., Steinmann, S., Dammermann, W., Lüth, S., Asghari, F., Wegscheid, C., Horst, A. K., et al. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1600418 · Cited by 53
Innate lymphoid cells in lung infection and immunity
Stehle, C., Hernández, D. C., & Romagnani, C. (2018) · Immunological Reviews · doi:10.1111/imr.12712 · Cited by 55
Xu, H., Wang, X., Lackner, A. A., & Veazey, R. S. (2015) · The FASEB Journal · doi:10.1096/fj.15-276477 · Cited by 52
Metabolic control of innate lymphoid cells in health and disease
Zhou, L., Lin, Q., & Sonnenberg, G. F. (2022) · Nature Metabolism · doi:10.1038/s42255-022-00685-8 · Cited by 53
The development of adult innate lymphoid cells
Yang, Q., & Bhandoola, A. (2016) · Current Opinion in Immunology · doi:10.1016/j.coi.2016.01.006 · Cited by 50
Self-citationInnate lymphoid cells in tissue homeostasis and diseases
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Transcription factor ISX mediates the cross talk between diet and immunity
Widjaja‐Adhi, M. A. K., Palczewski, G., Dale, K., Knauss, E. A., Kelly, M. E., Golczak, M., Levine, A. D., & Lintig, J. V. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1714963114 · Cited by 51
He, L., Zhou, M., & Li, Y. C. (2019) · iScience · doi:10.1016/j.isci.2019.06.026 · Cited by 52
Immunomodulatory role of oral microbiota in inflammatory diseases and allergic conditions
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Yang, J., Hu, S., Zhao, L., Kaplan, D. H., Perdew, G. H., & Xiong, N. (2016) · Nature Immunology · doi:10.1038/ni.3312 · Cited by 49
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Unconventional immune cells in the gut mucosal barrier: regulation by symbiotic microbiota
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Wan, T., Wang, Y., He, K., & Zhu, S. (2023) · Protein & Cell · doi:10.1093/procel/pwad028 · Cited by 50
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Zeng, L., Yang, K., Zhang, T., Zhu, X., Hao, W., Chen, H., & Ge, J. (2022) · Journal of Autoimmunity · doi:10.1016/j.jaut.2022.102919 · Cited by 47
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Cautivo, K. M., & Molofsky, A. B. (2016) · European Journal of Immunology · doi:10.1002/eji.201545562 · Cited by 43
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Schmidt, K. M., Haddad, E. N., Sugino, K. Y., Vevang, K. R., Peterson, L. A., Koratkar, R., Gross, M. D., Kerver, J. M., & Comstock, S. S. (2021) · Journal of Food Science · doi:10.1111/1750-3841.15586 · Cited by 44
Amino acid availability acts as a metabolic rheostat to determine the magnitude of ILC2 responses
Hodge, S. H., Krauss, M. Z., Kaymak, I., King, J. I., Howden, A. J. M., Panić, G., Grencis, R. K., Swann, J. R., Sinclair, L. V., & Hepworth, M. R. (2022) · The Journal of Experimental Medicine · doi:10.1084/jem.20221073 · Cited by 42
Dermal group 2 innate lymphoid cells in atopic dermatitis and allergy
Roediger, B., Kyle, R. L., Gros, G. S. L., & Weninger, W. (2014) · Current Opinion in Immunology · doi:10.1016/j.coi.2014.10.008 · Cited by 39
Impact of Micronutrients on the Immune Response of Animals
Smith, A. D., Panickar, K. S., Urban, J. F., & Dawson, H. D. (2018) · Annual Review of Animal Biosciences · doi:10.1146/annurev-animal-022516-022914 · Cited by 45
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Ohnmacht, C. (2016) · Trends in Immunology · doi:10.1016/j.it.2016.05.002 · Cited by 45
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Self-citationMcDaniel, K. L., Restori, K. H., Dodds, J. W., Kennett, M. J., Ross, A. C., & Cantorna, M. T. (2015) · Infection and Immunity · doi:10.1128/iai.00201-15 · Cited by 42
Microbiome modulates intestinal homeostasis against inflammatory diseases
Sun, X., & Jia, Z. (2018) · Veterinary Immunology and Immunopathology · doi:10.1016/j.vetimm.2018.10.014 · Cited by 44
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Michael, H., Amimo, J. O., Rajashekara, G., Saif, L. J., & Vlasova, A. N. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.826268 · Cited by 44
Crosstalk between the gut microbiota and innate lymphoid cells in intestinal mucosal immunity
Guo, Y., Liu, Y., Rui, B., Lei, Z., Ning, X., Liu, Y., & Li, M. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1171680 · Cited by 42
Group 2 innate lymphocytes at the interface between innate and adaptive immunity
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Metadata
- Authors
- Spencer, S. P., Wilhelm, C., Yang, Q., Hall, J. A., Bouladoux, N., Boyd, A., Nutman, T. B., Urban, J. F., Wang, J., Ramalingam, T. R., Bhandoola, A., Wynn, T. A., & Belkaid, Y.
- Affiliations
- National Institutes of Health (US)
- University of Pennsylvania (US)
- Helminth Immunology Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Disease, NIH, Bethesda, MD 20892, USA.
- Beltsville Human Nutrition Research Center (US)
- University of California, Berkeley (US)
- Corresponding author
- Spencer, S. P.
- Wilhelm, C.
- Belkaid, Y.
- Venue
- Science
- Published
- 2014-01-24
- Volume
- 343
- Issue
- 6169
- Pages
- 432-437
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC4313730
- OpenAlex
- W1999696784
- Cited by
- 447
- References
- 38
- Citations by year
- 2026: 14 · 2025: 23 · 2024: 25 · 2023: 31 · 2022: 33 · 2021: 24 · 2020: 29 · 2019: 44 · 2018: 36 · 2017: 43 · 2016: 40 · 2015: 56 · 2014: 48
- FWCI
- 28.46
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (Z99 AI999999)
- National Institute of Diabetes and Digestive and Kidney Diseases (F30DK094708)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › IL-33, ST2, and ILC Pathways
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Immune responses and vaccinations
- Keywords
- innate lymphoid cells, vitamin A deficiency, micronutrient deficiency, malnutrition, Th2 immune response, ILC3, ILC2, IL-13, intestinal immunity, barrier immunity, nematode infection, acute bacterial infection, immune adaptation
- MeSH terms
- Animals, Enterobacteriaceae Infections, Immunity, Innate, Lymphocytes, Mice, Inbred C57BL, Mice, Mutant Strains, Vitamin A, Vitamin A Deficiency, Homeodomain Proteins, Interleukin-13, Micronutrients, Citrobacter rodentium, Mice, Adaptive Immunity
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