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Maternal retinoids control type 3 innate lymphoid cells and set the offspring immunity
Open accessAbstract
The impact of nutritional status during fetal life on the overall health of adults has been recognized; however, dietary effects on the developing immune system are largely unknown. Development of secondary lymphoid organs occurs during embryogenesis and is considered to be developmentally programmed. Secondary lymphoid organ formation depends on a subset of type 3 innate lymphoid cells (ILC3) named lymphoid tissue inducer (LTi) cells. Here we show that mouse fetal ILC3s are controlled by cell-autonomous retinoic acid (RA) signalling in utero, which pre-sets the immune fitness in adulthood. We found that embryonic lymphoid organs contain ILC progenitors that differentiate locally into mature LTi cells. Local LTi cell differentiation was controlled by maternal retinoid intake and fetal RA signalling acting in a haematopoietic cell-autonomous manner. RA controlled LTi cell maturation upstream of the transcription factor RORγt. Accordingly, enforced expression of Rorgt restored maturation of LTi cells with impaired RA signalling, whereas RA receptors directly regulated the Rorgt locus. Finally, we established that maternal levels of dietary retinoids control the size of secondary lymphoid organs and the efficiency of immune responses in the adult offspring. Our results reveal a molecular link between maternal nutrients and the formation of immune structures required for resistance to infection in the offspring.
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“Besides the neurogenic potential of RA, recent studies have highlighted the critical role of RA in the derivation of embryonic hematopoietic cells9, lymphoid organs13, and Langerhans cells that reside specifically in the epidermis16.”
From Advances and challenges in retinoid delivery systems in regenerative and therapeutic medicine (2020) · cites this paper as [13]
In the citing paper
“the levels of retinoids obtained from the maternal diet increase the size of secondary lymphoid organs and the efficacy of adult immune responses13”
From Advances and challenges in retinoid delivery systems in regenerative and therapeutic medicine (2020) · cites this paper as [13]
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Cites
A global double-fluorescent Cre reporter mouse
Muzumdar, M. D., Tasic, B., Miyamichi, K., Li, L., & Luo, L. (2007) · genesis · doi:10.1002/dvg.20335 · Cited by 3,491
T cell receptor antagonist peptides induce positive selection.
Hogquist, K., Jameson, S., Heath, W., Howard, J. L., Bevan, M., & Carbone, F. (1994) · Cell · doi:10.1016/0092-8674(94)90169-4 · Cited by 3,252
Cre reporter strains produced by targeted insertion of EYFP and ECFP into the ROSA26 locus
Srinivas, S., Watanabe, T., Lin, C.-S., William, C. M., Tanabe, Y., Jessell, T. M., & Costantini, F. (2001) · BMC Developmental Biology · doi:10.1186/1471-213x-1-4 · Cited by 3,121
RAG-1-deficient mice have no mature B and T lymphocytes
Mombaerts, P., Iacomini, J., Johnson, R. S., Herrup, K., Tonegawa, S., & Papaioannou, V. E. (1992) · Cell · doi:10.1016/0092-8674(92)90030-g · Cited by 2,898
Living with the Past: Evolution, Development, and Patterns of Disease
Gluckman, P. D., & Hanson, M. A. (2004) · Science · doi:10.1126/science.1095292 · Cited by 1,917
Eberl, G., Marmon, S., Sunshine, M. J., Rennert, P. D., Choi, Y., & Littman, D. R. (2003) · Nature Immunology · doi:10.1038/ni1022 · Cited by 986
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
Yokota, Y., Mansouri, A., Mori, S., Sugawara, S., Adachi, S., Nishikawa, S., & Gruß, P. (1999) · Nature · doi:10.1038/17812 · Cited by 851
Natural aryl hydrocarbon receptor ligands control organogenesis of intestinal lymphoid follicles
Kiss, E. A., Vonarbourg, C., Kopfmann, S., Hobeika, E., Finke, D., Esser, C., & Diefenbach, A. (2011) · Science · doi:10.1126/science.1214914 · Cited by 801
Lee, J. S., Cella, M., McDonald, K. G., Garlanda, C., Kennedy, G. D., Nukaya, M., Mantovani, A., Kopan, R., Bradfield, C. A., Newberry, R. D., et al. (2012) · Nature Immunology · doi:10.1038/ni.2187 · Cited by 777
Cited by
Sorted by citations
Items 201–300 of 372
Complexity of cytokine network regulation of innate lymphoid cells in protective immunity
Seillet, C., Belz, G. T., & Mielke, L. A. (2014) · Cytokine · doi:10.1016/j.cyto.2014.06.002 · Cited by 29
Activity-Based Protein Profiling—Enabling Multimodal Functional Studies of Microbial Communities
Whidbey, C., & Wright, A. (2018) · Current topics in microbiology and immunology · doi:10.1007/82_2018_128 · Cited by 29
Crosstalk between epithelium, myeloid and innate lymphoid cells during gut homeostasis and disease
Ghilas, S., O’Keefe, R. N., Mielke, L. A., Raghu, D., Büchert, M., & Ernst, M. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.944982 · Cited by 30
Indrevær, R. L., Moskaug, J. Ø., Paur, I., Bøhn, S. K., Jørgensen, S. F., Blomhoff, R., Aukrust, P., Fevang, B., & Blomhoff, H. K. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1500250 · Cited by 28
TOX gene: a novel target for human cancer gene therapy.
Xin, Y., & Li, Z. (2015) · PubMed Central · Cited by 28
The S(c)ensory Immune System Theory
Veiga‐Fernandes, H., & Freitas, A. A. (2017) · Trends in Immunology · doi:10.1016/j.it.2017.02.007 · Cited by 28
Self-citationThe Impact of Maternal Microbes and Microbial Colonization in Early Life on Hematopoiesis
McCoy, K. D., & Thomson, C. A. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1701776 · Cited by 28
Burrows, K., Antignano, F., Chenery, A., Bramhall, M., Kořínek, V., Underhill, T. M., & Zaph, C. (2018) · PLoS Pathogens · doi:10.1371/journal.ppat.1006869 · Cited by 27
Dietary Derived Micronutrients Modulate Immune Responses Through Innate Lymphoid Cells
Shi, Z.-Z., Ohno, H., & Satoh‐Takayama, N. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.670632 · Cited by 27
Induction of cellular and molecular immunomodulatory pathways by vitamin A and flavonoids
Patel, S. P., & Vajdy, M. (2015) · Expert Opinion on Biological Therapy · doi:10.1517/14712598.2015.1066331 · Cited by 26
Retinoic acid signaling is essential for airway smooth muscle homeostasis
Chen, F. F., Shao, F., Hinds, A., Yao, S., Ram‐Mohan, S., Norman, T. A., Krishnan, R., & Fine, A. (2018) · JCI Insight · doi:10.1172/jci.insight.120398 · Cited by 26
The Metabolic Basis of ILC Plasticity
Pelletier, A., & Stockmann, C. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.858051 · Cited by 27
Group 3 innate lymphoid cells require BATF to regulate gut homeostasis in mice
Wu, X., Khatun, A., Kasmani, M. Y., Chen, Y., Zheng, S., Atkinson, S. N., Nguyen, C. P., Burns, R., Taparowsky, E. J., Salzman, N. H., et al. (2022) · The Journal of Experimental Medicine · doi:10.1084/jem.20211861 · Cited by 25
Shi, W.-N., Cui, S.-X., Song, Z.-Y., Wang, S.-Q., Sun, S.-Y., Yu, X.-F., Li, Y., Zhang, Y.-H., Gao, Z.-H., & Qu, X.-J. (2017) · Oncotarget · doi:10.18632/oncotarget.17174 · Cited by 24
Penkert, R. R., Smith, A. P., Hrincius, E. R., McCullers, J. A., Vogel, P., Smith, A. M., & Hurwitz, J. L. (2020) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiaa597 · Cited by 23
Metabolic Regulation of Group 3 Innate Lymphoid Cells and Their Role in Inflammatory Bowel Disease
Song, D., Lai, L., & Ran, Z. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.580467 · Cited by 22
Fernandes, S. B., Patil, N. D., Mériaux, S. B., Thérésine, M., Muller, C. P., Leenen, F. A. D., Elwenspoek, M. M. C., Zimmer, J., & Turner, J. D. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.674532 · Cited by 23
van Blijswijk, J., Schraml, B. U., Rogers, N. C., Whitney, P. G., Zelenay, S., Acton, S. E., & Sousa, C. R. E. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1401999 · Cited by 22
Role of group 3 innate lymphoid cells in antibody production
Magri, G., & Cerutti, A. (2015) · Current Opinion in Immunology · doi:10.1016/j.coi.2015.01.008 · Cited by 22
Sensing of physiological regulators by innate lymphoid cells
Seillet, C., & Jacquelot, N. (2019) · Cellular and Molecular Immunology · doi:10.1038/s41423-019-0217-1 · Cited by 22
Chen, B., Liu, S., Feng, D., Lu, X., Yang, T., Li, T., Sun, W., & Chen, J. (2020) · Frontiers in Nutrition · doi:10.3389/fnut.2020.580780 · Cited by 22
Innate lymphoid cell sensing of tissue vitality
Barrow, A. D., & Colonna, M. (2018) · Current Opinion in Immunology · doi:10.1016/j.coi.2018.11.004 · Cited by 22
Burger, N. B., Stuurman, K. E., Kok, E., Konijn, T., Schooneman, D. P. M., Niederreither, K., Coles, M. C., Agace, W. W., Christoffels, V. M., Mebius, R. E., et al. (2014) · Prenatal Diagnosis · doi:10.1002/pd.4473 · Cited by 21
Self-citationHeightened Immune Activation in Fetuses with Gastroschisis May Be Blocked by Targeting IL-5
Frascoli, M., Jeanty, C., Fleck, S., Moradi, P. W., Keating, S. M., Mattis, A. N., Tang, Q., & MacKenzie, T. C. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1502587 · Cited by 21
Spatial and temporal key steps in early‐life intestinal immune system development and education
Wagner, C., Torow, N., Hornef, M. W., & Lelouard, H. (2021) · FEBS Journal · doi:10.1111/febs.16047 · Cited by 22
Innate Lymphoid Cells: Important Regulators of Host–Bacteria Interaction for Border Defense
Beck, K., Ohno, H., & Satoh‐Takayama, N. (2020) · Microorganisms · doi:10.3390/microorganisms8091342 · Cited by 20
Layered origins of lymphoid tissue inducer cells
van de Pavert, S. A. (2023) · Immunological Reviews · doi:10.1111/imr.13189 · Cited by 22
Expanded ILC2s in human infant intestines promote tissue growth
Möller, K. J., Wegner, L. H. M., Malsy, J., Baumdick, M. E., Borggrewe, M., Jordan-Paiz, A., Jung, J. M., Martrus, G., Kretschmer, P., Sagebiel, A. F., et al. (2023) · Mucosal Immunology · doi:10.1016/j.mucimm.2023.04.004 · Cited by 20
Feeding immunity: skepticism, delicacies and delights
Veldhoen, M., & Veiga‐Fernandes, H. (2015) · Nature Immunology · doi:10.1038/ni.3100 · Cited by 20
Self-citationMucosal Immunity in HIV/SIV Infection: T Cells, B Cells and Beyond
Shacklett, B. L. (2018) · Current Immunology Reviews · doi:10.2174/1573395514666180528081204 · Cited by 21
Nakajima, A., Habu, S., Kasai, M., Okumura, K., Ishikawa, D., Shibuya, T., Kobayashi, O., Osada, T., Ohkusa, T., Watanabe, S., et al. (2020) · Bioscience of Microbiota Food and Health · doi:10.12938/bmfh.19-013 · Cited by 21
Dichotomous Regulation of Acquired Immunity by Innate Lymphoid Cells
Ebihara, T. (2020) · Cells · doi:10.3390/cells9051193 · Cited by 21
Bacteria-immune cells dialog and the homeostasis of the systems
Guzman-Bautista, E. R., Suzuki, K., Asami, S., & Fagarasan, S. (2020) · Current Opinion in Immunology · doi:10.1016/j.coi.2020.05.010 · Cited by 21
Neuro-immune-metabolism: The tripod system of homeostasis
Deshpande, D., Fuchs, L., & Klose, C. S. N. (2021) · Immunology Letters · doi:10.1016/j.imlet.2021.10.001 · Cited by 19
Identification of a novel lymphoid population in the murine epidermis
Almeida, F. F., Tenno, M., Brzostek, J., Li, J. L. Y., Allies, G., Hoeffel, G., See, P., Ng, L. G., Fehling, H. J., Gascoigne, N. R. J., et al. (2015) · Scientific Reports · doi:10.1038/srep12554 · Cited by 19
Self-citationSingh, A., Kazer, S. W., Roider, J., Krista, K. C., Millar, J. R., Asowata, O. E., Ngoepe, A., Ramsuran, D., Fardoos, R., Ardain, A., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.108153 · Cited by 19
Neuroepithelial VIP–VIPR1 interactions differentially control enteric type 1 and type 2 immunity
Pirzgalska, R. M., Henriques-Alves, B., Raposo, B., de Sousa, E., Torres, J., Ryu, J., Godinho‐Silva, C., Rendas, M. A., Pereira, M. E., Godinho, I., et al. (2025) · Nature Immunology · doi:10.1038/s41590-025-02326-0 · Cited by 18
Self-citationKumar, V. (2021) · International Reviews of Immunology · doi:10.1080/08830185.2021.1895145 · Cited by 19
Rodríguez‐Rodríguez, N., Clark, P. A., Gogoi, M., Ferreira, A. C. F., Kerscher, B., Crisp, A., Jolin, H. E., Murphy, J. E., Sivasubramaniam, M., Pedro, L., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2203454119 · Cited by 18
Thymic Program Directing the Functional Development of γδT17 Cells
Jouan, Y., Patin, E. C., Hassane, M., Si‐Tahar, M., Baranek, T., & Paget, C. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00981 · Cited by 19
Fontana, R., Raccosta, L., Rovati, L., Steffensen, K. R., Paniccia, A., Jakobsson, T., Melloni, G., Bandiera, A., Mangili, G., Bergamini, A., et al. (2018) · OncoImmunology · doi:10.1080/2162402x.2018.1554967 · Cited by 18
Thangavelu, G., Lee, Y., Loschi, M. L., Schaechter, K. M., Feser, C. J., Koehn, B. H., Nowak, E. C., Zeiser, R., Serody, J. S., Murphy, W. J., et al. (2019) · The Journal of Immunology · doi:10.4049/jimmunol.1800899 · Cited by 18
Nuclear hormone receptors put immunity on sterols
Santori, F. R. (2015) · European Journal of Immunology · doi:10.1002/eji.201545712 · Cited by 18
Self-citationEmbryonic ILC-poiesis across tissues
Hernández-Torres, D. C., & Stehle, C. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1040624 · Cited by 17
Bahmani, L., Baghi, M., Peymani, M., Javeri, A., & Ghaedi, K. (2021) · Human Cell · doi:10.1007/s13577-021-00558-4 · Cited by 18
Prenatal Diet and the Development of Childhood Allergic Diseases: Food for Thought
Pham, M. N., & Bunyavanich, S. (2018) · Current Allergy and Asthma Reports · doi:10.1007/s11882-018-0811-9 · Cited by 17
Cholesterol sensing and metabolic adaptation in tissue immunity
Dang, E. V., & Reboldi, A. (2024) · Trends in Immunology · doi:10.1016/j.it.2024.09.013 · Cited by 17
NK cell and ILC heterogeneity in colorectal cancer. New perspectives from high dimensional data
Pietropaolo, G., Scarno, G., Stabile, H., Grimaldi, A., Gismondi, A., Santoni, A., & Sciumè, G. (2021) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2021.100967 · Cited by 17
Innate immune cells link dietary cues to normal and abnormal metabolic regulation
Zhang, P., Watari, K., & Karin, M. (2025) · Nature Immunology · doi:10.1038/s41590-024-02037-y · Cited by 16
Colonization and effector functions of innate lymphoid cells in mucosal tissues
Kim, M., & Kim, C. H. (2016) · Microbes and Infection · doi:10.1016/j.micinf.2016.06.005 · Cited by 16
Innate lymphoid cell and adaptive immune cell cross-talk: A talk meant not to forget
Kumar, V. (2020) · Journal of Leukocyte Biology · doi:10.1002/jlb.4mir0420-500rrr · Cited by 16
Brandtzæg, P. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-415847-4.00031-8 · Cited by 16
Zhou, Z., Lv, Y., Zuo, A., Zhu, X., Xu, Y., Zuo, L., Xu, H., Liu, S., Zhang, Y., Weng, S., et al. (2025) · hLife · doi:10.1016/j.hlife.2025.05.008 · Cited by 15
Huang, J., Zhang, J., Wang, X., Jin, Z., Zhang, P., Su, H., & Sun, X. (2022) · Kompass Neumología · doi:10.1159/000525449 · Cited by 17
Li, X., Wang, M., Liu, S., Chen, X., Qiao, Y., Yang, X., Yao, J., & Wu, S. (2022) · Animal nutrition · doi:10.1016/j.aninu.2022.07.002 · Cited by 16
Bastos-Amador, P., Duarte, E. L., Torres, J., Caldeira, A. T., Silva, I., Salvador, C., Assunção, R., Alvito, P., & Ferreira, M. M. (2023) · Food and Chemical Toxicology · doi:10.1016/j.fct.2022.113596 · Cited by 16
Self-citationMirpuri, J. (2021) · Oxford Open Immunology · doi:10.1093/oxfimm/iqab009 · Cited by 14
Vitamins as influenza vaccine adjuvant components
Quintilio, W., de Freitas, F. A., Rodriguez, D., Kubrusly, F. S., Yourtov, D., Miyaki, C., Leite, L. C. C., & Raw, I. (2016) · Archives of Virology · doi:10.1007/s00705-016-2994-5 · Cited by 14
The Role of Micronutrients in Graft-VS.-Host Disease: Immunomodulatory Effects of Vitamins A and D
Chen, X., & Mayne, C. G. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02853 · Cited by 14
An Essential Role of Innate Lymphoid Cells in the Pathophysiology of Graft-vs.-Host Disease
Shao, L., Pan, S., Zhang, Q., Jamal, M., Chen, L., Yin, Q., Wu, Y., Xiong, J., Xiao, R., Kwong, Y., et al. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01233 · Cited by 14
Group 3 innate lymphoid cells: A trained Gutkeeper
Serafini, N., & Santo, J. P. D. (2024) · Immunological Reviews · doi:10.1111/imr.13322 · Cited by 14
Pirker, A.-L., & Vogl, T. J. (2024) · Frontiers in Allergy · doi:10.3389/falgy.2024.1439303 · Cited by 15
Inherited nongenetic influences on the gut microbiome and immune system
Knoop, K. A., Holtz, L. R., & Newberry, R. D. (2018) · Birth Defects Research · doi:10.1002/bdr2.1436 · Cited by 13
Type 3 innate lymphoid cells are altered in colons of C57BL/6 mice with dioxin exposure
Li, Y., Xie, H. Q., Zhang, W., Wei, Y., Sha, R., Xu, S. L., Zhang, J., Jiang, Y., Guo, T. L., & Zhao, B. (2019) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2019.01.139 · Cited by 13
Roberts, L. B., Kelly, A. M., & Hepworth, M. R. (2025) · Mucosal Immunology · doi:10.1016/j.mucimm.2025.01.012 · Cited by 12
Zhou, P., Zheng, T., Li, Y., Zhang, X., Feng, J., Wei, Y., Wang, H., Yao, Y., Gong, F., Tian, W., et al. (2020) · Environmental Science & Technology · doi:10.1021/acs.est.0c03758 · Cited by 12
Actions of Retinoic Acid in the Pathophysiology of HIV Infection
Sidell, N., & Kane, M. A. (2022) · Nutrients · doi:10.3390/nu14081611 · Cited by 14
Charmetant, X., Bachelet, T., Déchanet‐Merville, J., Walzer, T., & Thaunat, O. (2021) · Transplantation · doi:10.1097/tp.0000000000003782 · Cited by 14
Almeida, A. R. M., Fonseca‐Pereira, D., Arroz‐Madeira, S., Ribeiro, H., Labão‐Almeida, C., & Veiga‐Fernandes, H. (2014) · European Journal of Immunology · doi:10.1002/eji.201344422 · Cited by 13
Self-citationWang, Y., Zhang, Y., Kim, K., Han, J., Okin, D. A., Jiang, Z., Yang, L., Subramaniam, A., Means, T. K., Nestle, F. O., et al. (2024) · Immunity · doi:10.1016/j.immuni.2024.10.010 · Cited by 11
Vallecillo-García, P., Orgeur, M., Comai, G., Pöhle‐Kronawitter, S., Fischer, C., Gloger, M., Dumas, C. E., Giesecke‐Thiel, C., Sauer, S., Tajbakhsh, S., et al. (2022) · Immunity · doi:10.1016/j.immuni.2023.04.014 · Cited by 11
Intestinal factors promoting the development of RORγt+ cells and oral tolerance
López‐Fandiño, R., Molina, E., & Lozano‐Ojalvo, D. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1294292 · Cited by 11
Novel Perspective on the Regulation of Offspring Food Allergy by Maternal Diet and Nutrients
Bai, T., Wang, Z., Shao, H., Zhang, X., Lorenz, A., Meng, X., Wu, Y., Chen, H., & Li, X. (2024) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.3c09108 · Cited by 11
Do advanced glycation end-products play a role in malaria susceptibility?
Traoré, K., Arama, C., Médebielle, M., Doumbo, O. K., & Picot, S. (2016) · Parasite · doi:10.1051/parasite/2016015 · Cited by 11
Lin, Y., Leung, G., Louie, D., Bogoslowski, A., Ross, J., Kubes, P., von der Weid, P., & Liao, S. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1800151 · Cited by 11
Development of follicular dendritic cells in lymph nodes depends on retinoic acid-mediated signaling
Koning, J. J., Rajaraman, A., Reijmers, R. M., Konijn, T., Pan, J., Ware, C. F., Butcher, E. C., & Mebius, R. E. (2021) · Development · doi:10.1242/dev.199713 · Cited by 11
Self-citationLi, J., Yu, Y., Miao, T., Wang, H., Wei, F., Li, L., & Wang, X. (2006) · PubMed · Cited by 11
The metabolic sensor LKB1 regulates ILC3 homeostasis and mitochondrial function
Fonseca‐Pereira, D., Bae, S., Clay, S. L., Michaud, M., MacDonald, M. H., Glickman, J. N., & Garrett, W. S. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115456 · Cited by 10
Profiling the diversity of innate lymphoid cells
Diefenbach, A. (2015) · Nature Immunology · doi:10.1038/ni.3107 · Cited by 10
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Cairo, C., & Webb, T. J. (2022) · The Journal of Immunology · doi:10.4049/jimmunol.2100799 · Cited by 10
Development of Gut-Associated Lymphoid Tissues
Flach, M., & Diefenbach, A. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-415847-4.00003-3 · Cited by 10
Almeida, F. F., Jacquelot, N., & Belz, G. T. (2018) · Immunological Reviews · doi:10.1111/imr.12709 · Cited by 10
Self-citationHan, J., & Jang, K. L. (2023) · Viruses · doi:10.3390/v15071456 · Cited by 9
Human Milk Drives the Intimate Interplay Between Gut Immunity and Adipose Tissue for Healthy Growth
van den Elsen, L. W. J., & Verhasselt, V. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.645415 · Cited by 9
Innate lymphoid cells—key immune integrators of overall body homeostasis
Karagiannis, F., & Wilhelm, C. (2018) · Seminars in Immunopathology · doi:10.1007/s00281-018-0684-y · Cited by 9
Poniewierska-Baran, A., Tokarz–Deptuła, B., & Deptuła, W. (2019) · Archives of Medical Science · doi:10.5114/aoms.2019.89835 · Cited by 10
Michita, R. T., Jimenez, N. R., Herbst‐Kralovetz, M. M., & Mysorekar, I. U. (2026) · Infection and Immunity · doi:10.1128/iai.00608-25 · Cited by 9
Association of vitamin A supplementation with immune-related allergic diseases: A meta-analysis
Su, J., Li, T., & Pan, H. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.984161 · Cited by 8
Xavier‐Elsas, P., Vieira, B. M., Masid‐de‐Brito, D., Santos, J., Barradas, M., de Luca, B., & Elsas, M. (2017) · International Immunopharmacology · doi:10.1016/j.intimp.2017.02.001 · Cited by 8
Mechanisms of gastrointestinal pathogenesis and landscape of intestinal immunity
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Metadata
- Authors
- van de Pavert, S. A., Ferreira, M., Domingues, R. G., Ribeiro, H., Molenaar, R., Moreira-Santos, L., Almeida, F. F., Ibiza, S., Barbosa, I., Goverse, G., Labão-Almeida, C., Godinho-Silva, C., Konijn, T., Schooneman, D., O’Toole, T., Mizee, M. R., Habani, Y., Haak, E., Santori, F. R., Littman, D. R., Schulte-Merker, S., Dzierzak, E., Simas, J. P., Mebius, R. E., & Veiga-Fernandes, H.
- Affiliations
- Instituto de Medicina Molecular João Lobo Antunes (PT)
- University of Lisbon (PT)
- Amsterdam UMC Location Vrije Universiteit Amsterdam (NL)
- Erasmus MC (NL)
- Howard Hughes Medical Institute (US)
- ORCID
- Venue
- Nature
- Published
- 2014-03-19
- Volume
- 508
- Issue
- 7494
- Pages
- 123-127
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC4932833
- OpenAlex
- W2076363780
- Cited by
- 374
- References
- 42
- Citations by year
- 2026: 11 · 2025: 20 · 2024: 15 · 2023: 25 · 2022: 26 · 2021: 21 · 2020: 33 · 2019: 34 · 2018: 48 · 2017: 24 · 2016: 39 · 2015: 47 · 2014: 30
- FWCI
- 21.33
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Amsterdam UMC (VU Amsterdam) - Institutional Repository (publishedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (publishedVersion)
- PubMed Central (acceptedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- Minerva Access (University of Melbourne) (submittedVersion)
- Pure Amsterdam UMC (submittedVersion)
- KNAW Research Portal (The Royal Netherlands Academy of Arts and Sciences) (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- Crohn's and Colitis Foundation (313089)
- National Institute of Allergy and Infectious Diseases (R01AI080885)
- 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
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Birth, Development, and Health
- Keywords
- retinoic acid, ILC3, lymphoid tissue inducer cells, fetal immune development, RORγt, retinoic acid receptor, maternal nutrition
- MeSH terms
- Animals, Cell Differentiation, Diet, Female, Fetus, Immunity, Innate, Lymphoid Tissue, Mice, Inbred C57BL, Pregnancy, Prenatal Exposure Delayed Effects, Stem Cells, Tretinoin, Signal Transduction, Receptors, Retinoic Acid, Mice
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