The DOI matches its Crossref record; 164 of the 167 references it cites were found in a registry or an index.
Epithelial-cell recognition of commensal bacteria and maintenance of immune homeostasis in the gut
Abstract
Mucosal surfaces such as the intestinal tract are continuously exposed to both potential pathogens and beneficial commensal microorganisms. This creates a requirement for a homeostatic balance between tolerance and immunity that represents a unique regulatory challenge to the mucosal immune system. Recent findings suggest that intestinal epithelial cells, although once considered a simple physical barrier, are a crucial cell lineage for maintaining intestinal immune homeostasis. This Review discusses recent findings that identify a cardinal role for epithelial cells in sampling the intestinal microenvironment, discriminating pathogenic and commensal microorganisms and influencing the function of antigen-presenting cells and lymphocytes.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“The host-microbiota relationship has been defined as the synergistic effect of microbial metabolites on host immunity, health and disease, energy metabolism, and cellular communication.59, 60, 61, 62, 63,64”
From Regulation of Intestinal Barrier Function by Microbial Metabolites (2021) · cites this paper as [64]
Citations
Cites
Human gut microbes associated with obesity
Ley, R. E., Turnbaugh, P. J., Klein, S., & Gordon, J. I. (2006) · Nature · doi:10.1038/4441022a · Cited by 8,785
Diversity of the Human Intestinal Microbial Flora
Eckburg, P. B., Bik, E. M., Bernstein, C. N., Purdom, E., Dethlefsen, L., Sargent, M., Gill, S. R., Nelson, K. E., & Relman, D. A. (2005) · Science · doi:10.1126/science.1110591 · Cited by 7,913
The gut microbiota as an environmental factor that regulates fat storage
Bäckhed, F., Ding, H., Wang, T., Hooper, L. V., Koh, G. Y., Nagy, A., Semenkovich, C. F., & Gordon, J. I. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0407076101 · Cited by 6,245
Obesity alters gut microbial ecology
Ley, R. E., Bäckhed, F., Turnbaugh, P., Lozupone, C. A., Knight, R. D., & Gordon, J. I. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504978102 · Cited by 6,176
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
Hugot, J.-P., Chamaillard, M., Zouali, H., Lesage, S., Cézard, J.-P., Belaiche, J., Almer, S., Tysk, C., O'Morain, C. A., Gassull, M., et al. (2001) · Nature · doi:10.1038/35079107 · Cited by 5,591
Host-Bacterial Mutualism in the Human Intestine
Bäckhed, F., Ley, R. E., Sonnenburg, J. L., Peterson, D. A., & Gordon, J. I. (2005) · Science · doi:10.1126/science.1104816 · Cited by 5,277
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
Ogura, Y., Bonen, D. K., Inohara, N., Nicolae, D. L., Chen, F. F., Ramos, R., Britton, H., Moran, T., Karaliuskas, R., Duerr, R. H., et al. (2001) · Nature · doi:10.1038/35079114 · Cited by 5,030
Prokaryotes: The unseen majority
Whitman, W. B., Coleman, D. C., & Wiebe, W. J. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.12.6578 · Cited by 4,871 · cited 1×
“In addition, the collective genetic material of commensal communities, termed the microbiome and which encompasses at least 500–1000 species, is thought to encode as much as 100 times the number of genes in the human genom”
BackgroundPhosphorylation meets ubiquitination: the control of NF-κB activity
Karin, M., & Ben-Neriah, Y. (2000) · Annual Review of Immunology · doi:10.1146/annurev.immunol.18.1.621 · Cited by 4,766
Metagenomic Analysis of the Human Distal Gut Microbiome
Gill, S. R., Pop, M., DeBoy, R. T., Eckburg, P. B., Turnbaugh, P. J., Samuel, B. S., Gordon, J. I., Relman, D. A., Fraser-Liggett, C. M., & Nelson, K. E. (2006) · Science · doi:10.1126/science.1124234 · Cited by 4,699
Flagged first, then by citations
3 of the 167 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Items 901–1,000 of 1,000
Molecular analysis of candidate probiotic effector molecules of Lactobacillus plantarum
Remus, D. M. (2012) · doi:10.18174/232424 · Cited by 2
“Several proteomics-based studies have addressed the molecular mechanisms behind the interactions between lactobacilli and their environments, which include adaption to fermentation and GI tract conditions (59-63) and lactobacillus-host interactions within the framework of probiotic function (64, 65).”
BackgroundClostridium difficile infection in neonatal piglets: Pathogenesis, risk factors, and prevention
Arruda, P. (2014) · doi:10.31274/etd-180810-3641 · Cited by 2
“During the piglet’s life, several other microbes compete for places in microbial niches in a process of succession that eventually establishes the flora, consisting of well over 500 distinct species of bacteria in the mature gastrointestinal tract (Artis, 2008).”
BackgroundLa reconnaissance des bactéries de la flore intestinale
Villani, A., & Franchimont, D. P. (2010) · médecine/sciences · doi:10.1051/medsci/201026136 · Cited by 2
In vitro fermentation and immunomodulating characteristics of dietary fibres
Rösch, C. (2016) · doi:10.18174/379397 · Cited by 2
Huang, Y., Yu, Y., Zhan, S., Tomberlin, J. K., Huang, D., Cai, M., Zheng, L., Yu, Z., & Zhang, J. (2019) · doi:10.21203/rs.2.10196/v1 · Cited by 2
Dualib, P. M., Fernandes, G. D. R., Taddei, C. R., Carvalho, C. R. D. S., Sparvoli, L. G., Bittencourt, C., da Silva, I. T., Mattar, R., Ferreira, S. R. G., Dib, S. A., et al. (2022) · Research Square · doi:10.21203/rs.3.rs-1938616/v1 · Cited by 2
The anti-adipogenic effects of postbiotics derived from plant-based lactic acid bacteriaPreprint
Yoon, D. H., Kim, J. Y., Keon, H., Lee, H. G., Seo, K., Shim, J.-J., Lee, J.-L., & Kim, H. (2022) · Research Square · doi:10.21203/rs.3.rs-2052815/v1 · Cited by 2
Yunker, R., Han, G., Vasquez, J., Baldaro, K., Zhang, L., Lee, S., & Vaishnava, S. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.05.07.652635 · Cited by 2
Probiotics effect in prevention and treatment of atopic dermatitis and eczema in children
Dima, V., Iancu, G., Bohîlțea, R. E., Toma, A. I., Avramescu-Calomfirescu, A., Varlas, V. N., & Daviţoiu, A. M. (2022) · Romanian Journal of Pharmaceutical Practice · doi:10.37897/rjphp.2022.2.4 · Cited by 1
Anandh, U., & Saxena, A. (2024) · Journal of Renal Nutrition and Metabolism · doi:10.4103/jrnm.jrnm_1_23 · Cited by 1
Abdurasulova, I. N. (2024) · Medical academic journal · doi:10.17816/maj633511 · Cited by 1
Jasmine, Samtiya, M., Rodrigues, R., Mandal, A., Kavya, T. T., Anushree, A., Lafin, J. T., Vezina, C. M., Strand, D. W., & Joseph, D. B. (2025) · Mucosal Immunology · doi:10.1016/j.mucimm.2025.09.001 · Cited by 4
“Signals from specialized tissue compartments at mucosal sites can influence macrophage localization and functional diversification 18,19 .”
Evaluating preservation effects on honeybee gut microbiota inocula
Wang, K., Xu, Z., Ma, J., Zheng, M. F., Zhang, Y., Lin, Z., & Ji, T. (2025) · Microbiology Spectrum · doi:10.1128/spectrum.02754-25 · Cited by 1
Chen, B., Gg, C., Leng, X., Li, Q., Wu, W., Wu, W., Liu, Z., Zhong, Z., Zheng, X., Kang, W., et al. (2026) · Advanced Science · doi:10.1002/advs.202519949 · Cited by 2
Zhang, M., Du, M., Zhang, W., Huang, R., Li, W., Li, T., Bai, J., Zhang, N., Chen, J., Zhou, J., et al. (2026) · iMetaMed · doi:10.1002/imm3.70033 · Cited by 1
Gut Microbiota Mediates HFPO–DA-Induced Hepatotoxicity via Arginine Reprogramming in Lean NAFLD Mice
Ding, R., He, L., Guo, R., Tian, X., Chen, L., Zhan, N., Chen, L., Wu, Y., ZHANG, J., & Zhao, F. (2026) · Environmental Science & Technology · doi:10.1021/acs.est.6c02839 · Cited by 1
When Small Meets Smaller: Immune Modulation and Virulence Strategies in Insect–Bacteria Interactions
Bianchi, T., Mastore, M., Banfi, D., Loulou, A., Quadroni, S., & Brivio, M. (2026) · Insects · doi:10.3390/insects17050515 · Cited by 1
“Recent studies across multiple animal models have demonstrated a dynamic, bidirectional interaction between the gut microbiota and the host immune system: the immune system shapes microbial composition, while resident microbes influence immune function and responsiveness [30].”
Zhu, D. K., Wen, N., Peng, K. Y., Jiang, L. L., Li, J., & Zhao, L. (2026) · Ecology and Evolution · doi:10.1002/ece3.73993 · Cited by 1
Intestinal Epithelial MHC-II at the Interface of Microbiota, Immunity, and Inflammation
de Oliveira, S., & Fachi, J. L. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27167271 · Cited by 1
“…primarily separate host tissues from the external environment, the intestinal epithelium is continuously exposed to an immense and highly diverse antigenic burden that includes dietary proteins, commensal microorganisms, microbial metabolites, environmental antigens, and enteric pathogens [1].”
The Roles of Interleukin-17 and T Helper 17 Cells in Intestinal Barrier Function
Trusevych, E., Mortimer, L. M., & Chadee, K. (2012) · InTech eBooks · doi:10.5772/29441 · Cited by 1
“From there, dendritic cells move into local T cell/follicular areas or drain to the MLN to initiate adaptive responses (Artis, 2008; Kelsall, 2008; Mowat, 2003).”
BackgroundMathews, S., Panicker, S., Arunkumar, G. R., & Mathew, T. V. (2015) · Cited by 1
DIET, BACTERIA AND INFLAMMATION: THE INTESTINAL MUCOSA AND METABOLIC SYNDROME
Mohammed, N. (2012) · UKnowledge (University of Kentucky) · Cited by 1
Helmy, M., Alafifi, A. M., & Ali, A. H. (2009) · PubMed · Cited by 1
New Probiotics: Dairy Propionibacteria and the Modulation of Gut Microbiota and Physiology
(2014) · CRC Press eBooks · doi:10.1201/b16439-8 · Cited by 1
Analytical Methodologies of Chitosan in Functional Foods
Liu, Y., Bai, Y., & Liu, H. (2012) · CRC Press eBooks · doi:10.1201/b11653-28 · Cited by 1
Sandeep, P., & Kumari, P. (2016) · International Journal of Pharma and Bio Sciences · Cited by 1
Health Benefits of Human Probiont Lactobacillus plantarum
Ramraj, S. K., & Arul, V. (2015) · CRC Press eBooks · doi:10.1201/b19308-55 · Cited by 1
Kolling, J. (2014) · Cited by 1
Intestinal microbiota around colorectal cancer genesis
Brandi, G., Rosa, F. D., Liguori, G., Agostini, V., Girolamo, S. D., Gaboriau‐Routhiau, V., Raibaud, P., & Biasco, G. (2013) · Archivio istituzionale della ricerca (Alma Mater Studiorum Università di Bologna) · Cited by 1
Cellular Organization of the Gastrointestinal Tract
Welcome, M. O. (2018) · Springer eBooks · doi:10.1007/978-3-319-91056-7_3 · Cited by 3
Cesarean section. Is the choice justified? Risks to children’s health
Zakharova, I. N., Osmanov, I. M., Berezhnaya, I. V., Анатольевич, К. К., Dedikova, O. V., Kuchina, A. E., Sazanova, Y. О., & Мартыненко, Л. Е. (2018) · Meditsinskiy sovet = Medical Council · doi:10.21518/2079-701x-2018-17-16-21 · Cited by 1
Silva, C., Eremina, Y. O., Rodrigues, S. G., Coelho, R., Ramalho, R., Lopes, O., Carneiro, F., & Simões, J. S. (2018) · PubMed · doi:10.1016/j.pbj.0000000000000022 · Cited by 1
The role of intestinal flora in autism and nutritional approaches
Ekmekçi, A. M. (2020) · Demiroglu Science University Florence Nightingale Transplantation Journal · doi:10.5606/dsufnjt.2020.017 · Cited by 1
“Allergies can be observed as a result of increased immune activation against these antigens that enter the systemic circulation.[30,31] Environmental stress and high pro-inflammatory cytokines”
BackgroundProbiotics and human gut microbiota modulation
Sinisterra-Loaiza, L., Lamas, A., Miranda, J. M., Cepeda, A., & Cardelle‐Cobas, A. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-89908-6.00024-8 · Cited by 1
Benefits and safety of probiotics in gastrointestinal diseases
Profir, M., Roşu, O. A., Ionescu, R. F., Pavelescu, L. A., & Creţoiu, S. M. (2024) · Elsevier eBooks · doi:10.1016/b978-0-12-824472-2.00011-7 · Cited by 1
Anandh, U., & Saxena, A. (2023) · Journal of Renal Nutrition and Metabolism · doi:10.4103/jrnm.jrnm_6_23 · Cited by 1
Thomas, D. M., & O’Connor, G. (2025) · Journal of Child Health Care · doi:10.1177/13674935251355323 · Cited by 1
Mukosale Homöostase und orale Toleranz
Allam, J., & Novak, N. (2013) · Allergo Journal · doi:10.1007/s15007-013-0222-0 · Cited by 1
Factors Involved in Onset of Type 1 Diabetes
Cooke, A., & Zaccone, P. (2012) · Molecular and integrative toxicology · doi:10.1007/978-1-61779-812-2_6 · Cited by 1
The Intestinal Immune System in Health
Brandtzæg, P. (2011) · Springer eBooks · doi:10.1007/978-1-4614-0998-4_3 · Cited by 1
Role of the Gut Microbiota in Maintaining GI Health: Highlights on Inflammatory Bowel Disease
Gruber, L., & Haller, D. (2014) · Molecular and integrative toxicology · doi:10.1007/978-1-4471-6539-2_13 · Cited by 1
Nutritional Adequacy and Performance of Raw Food Diets in Kittens
Hamper, B. A. (2012) · Cited by 1
Immunopathogenic aspects of resolving and progressing appendicitis
Rubèr, M. (2012) · Cited by 1
ER Stress in Intestinal Inflammatory Disease
Tomczak, M. F., Kaser, A., & Blumberg, R. S. (2012) · Springer eBooks · doi:10.1007/978-94-007-4351-9_12 · Cited by 1
Martynov, V. L., & Khairdinov, A. K. (2015) · Bulletin of Siberian Medicine · doi:10.20538/1682-0363-2015-3-49-62 · Cited by 1
Epigenetics and the Microbiome
Pevsner‐Fischer, M., Zmora, N., Braverman, S., & Elinav, E. (2017) · Springer eBooks · doi:10.1007/978-3-319-31143-2_35-1 · Cited by 1
Microbial sensing in the neonatal pig gut: effect of diet-independent and diet-dependent factors1
Wellington, M. O., Agyekum, A. K., & Kessel, A. G. V. (2021) · Canadian Journal of Animal Science · doi:10.1139/cjas-2020-0051 · Cited by 1
“Host sensing of microbial components is achieved through the detection of molecular patterns unique to microbiota [termed microbiota-associated molecular patterns (MAMP)] by families of host pattern recognition receptors (PRR) present on epithelial cells and immune cells (Sellge and Kufer 2015).”
BackgroundInfluentialLymphoma Caused by Intestinal Microbiota
Yamamoto, M. L., & Schiestl, R. H. (2014) · Cancer and Oncology Research · doi:10.13189/cor.2014.020601 · Cited by 1
The Effects of Oral Controlled Exposure on Colostrum Characteristics in Swine
Arruda, P. (2010) · doi:10.31274/etd-180810-921 · Cited by 1
“The tightly organized intestinal epithelial cell (IEC) junctions form an effective physical barrier against microorganisms (Artis, 2008; Burkey, 2009) as well as facilitating the presentation and transfer of potential antigens to the cells located in the GALT.”
InfluentialDefining innate immunity to Clostridium difficile
Jafari, N. V. (2012) · UCL Discovery (University College London) · Cited by 1
Commentary: vancomycin or metronidazole in patients with primary sclerosing cholangitis?
Paterson, J. C. M., & Dillon, J. F. (2013) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.12282 · Cited by 1
On the regulation of immune responses to dietary and self antigens
Lindgrén, S. (2010) · Gothenburg University Publications Electronic Archive (Gothenburg University) · Cited by 1
To Move or to Convene : Regulatory Circuits of Mat Fimbriae in Escherichia coli
Lehti, T. A. (2012) · Työväentutkimus Vuosikirja · Cited by 1
Dietary immune-modulation – carbohydrate specific effects of cereal and yeast beta-glucans
Rieder, A. (2013) · NORA - Norwegian Open Research Archives · Cited by 1
Intestinal natural killer cells
Goodier, M. R. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-370454-2.00025-9 · Cited by 1
Francescone, R. A., III, & Costa, D. B. V. (2016) · doi:10.1002/9781118982907.ch25 · Cited by 1
Kong, S., & Zhang, W. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/186023 · Cited by 1
“IEC can form a continuous physical barrier that separate mammalian hosts from the external environment[1][2], and has diverse functions including physical segregation of commensal bacteria and the integration of microbial signals: form a barrier in the intestine to prevent the entrance of harmful substances; secrete d…”
Backgroundvan der Eijk, J. A. J. (2019) · doi:10.18174/502550 · Cited by 1
The Role of Bovine Cathelicidins in Host Defence
Paget, B. W. (2014) · Open Access Victoria University of Wellington | Te Herenga Waka (Figshare) · doi:10.26686/wgtn.17006605 · Cited by 1
“In the gastrointestinal tract, peristalsis helps to remove pathogens and the intestinal mucosa allows colonisation by commensal bacteria, which helps to prevent colonisation by pathogens through competition for nutrients and excretion of compounds that are toxic to pathogens [16].”
BackgroundCham, C. M., Messer, J. S., Lake, J., Zhu, X., Tao, Y., He, L., Weber, C. R., Lin, F., Dai, Z., Tong, J., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.06.30.498349 · Cited by 1
Development of the gut microbiota during early life in premature and term infantsPreprint
Sim, K., Powell, E. A., Cornwell, E., Kroll, J. S., & Shaw, A. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.07.24.501289 · Cited by 1
Differences in gut metagenomes between dairy workers and community controls: a cross-sectional studyPreprint
Trinh, P., Roberts, M. C., Rabinowitz, P. M., & Willis, A. D. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.10.540270 · Cited by 1
“…has facilitated the study of entire microbial communities of culturable and unculturable microorganisms, revealing the profound impact that the human gut microbiome has on immune homeostasis [4, 5, 36], disease development [17, 30, 60, 91], and even resistance to pathogen invasion [1, 10, 39, 41].”
Wisner, A. L. S. (2011) · University Library - University of Saskatchewan (University of Saskatchewan)
Jiang, H. (2010) · Iowa State University Digital Repository (Iowa State University) · doi:10.31274/etd-180810-1957
“They form resistance to pathogen colonization via producing antimicrobial substances, changing luminal pH and directly competing against pathogens for nutrients, thereby obstructing and inhibiting pathogen invasion (11, 12).”
BackgroundMass spectrometric–based protein chips for detection of food‐derived bioactive components
Stagsted, J., Jørgensen, A. L. W., & Juul‐Madsen, H. R. (2010) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.05258.x
Brown, M. (2012) · Nottingham ePrints (University of Nottingham)
Microbial regulation of allergic inflammation
Hill, D. A. (2011) · Scholarly Commons (University of Pennsylvania)
The Role of TCR Specificity in the Regulation of the Immune Response to Self and Commensal Antigens
Lathrop, S. K. (2010) · Open Scholarship Institutional Repository (Washington University in St. Louis) · doi:10.7936/k7vd6wf0
“for the normal development of both the mucosal and peripheral immune system [85].”
BackgroundModulation of immune responses by commensal bacteria and intestinal helminth
Tina, H. (2011) · Repository for Publications and Research Data (ETH Zurich) · doi:10.3929/ethz-a-007084676
Acquired Immunity to Helminths
Artis, D., & Maizels, R. M. (2014) · ASM Press eBooks · doi:10.1128/9781555816872.ch25
Safroneeva, E. (2009) · MacSphere (McMaster University) · doi:10.71548/10686
Physiologie und Pathophysiologie des Immunsystems
Fleischer, B. (2010) · Springer eBooks · doi:10.1007/978-3-642-12765-6_5
Anatomy of the Gut Barrier and Establishment of Intestinal Homeostasis
Sellge, G., Schnupf, P., & Sansonetti, P. J. (2010) · Wiley eBooks · doi:10.1002/9783527629664.ch10
Sigurdardottir, S. L. (2014) · Skemman
Potencialidad probiótica de lactobacilos con capa S
Carasi, P. (2014) · El Servicio de Difusión de la Creación Intelectual (National University of La Plata) · doi:10.35537/10915/43573
Standing Guard: Innate Lymphoid Cells Promote Immunity and Tissue Homeostasis at Barrier Surfaces
Monticelli, L. A., & Artis, D. (2013) · Else Kröner-Fresenius Symposia · doi:10.1159/000346504
Proceedings from the FFF Probiotics 2012 meeting in Turku, Finland, 11–13 June 2012
(2012) · Microbial Ecology in Health and Disease · doi:10.3402/mehd.v23i0.18868
Microbial Programming of the Neonatal Pig
Petri, D. (2013) · HARVEST (University of Saskatchewan)
Plant-derived compounds in experimental inflammatory bowel disease and colon carcinogenesis
Fasolino, I. (2013) · Università degli Studi di Napoli Federico II · doi:10.6092/unina/fedoa/9341
Ng, Y. L. (2012) · Murdoch University Research Portal
Roche, R. (2011) · White Rose eTheses Online (University of Leeds, The University of Sheffield, University of York)
The ontogeny and function of intestinal dendritic cells
Persson, E. K. (2014) · Lund University Publications (Lund University)
Phenotype and function of intestinal CD103+ dendritic cells
Gyllenbäck, E. J. (2011) · Lund University Publications (Lund University)
Dang, T. N.-D. (2012) · Deep Blue (University of Michigan)
Adapt, Survive or Die - Metabolic Imbalances and the Enteric Nervous System
Voss, U. (2013) · Lund University Publications (Lund University)
Microbiota and immunity: from preclinical data to clinical practice
Giannetti, E., & Staiano, A. (2015) · Journal of pediatric and neonatal individualized medicine · doi:10.7363/040233
“This interaction between gut microbiota and epithelial and lymphoid cells results in the expression of a number of molecules, which mediate host defense or metabolic activities within the intestine [11].”
BackgroundEarly Life Intestinal Microbiota in Health and in Atopic Eczema
Nylund, L. (2015) · UTUPub (University of Turku)
Regulation and role of IL-7 production in HIV-1 infection
Thắng, P. H. (2011) · Figshare
Jirillo, F., Jirillo, E., & Magrone, T. (2011) · Mediterranean Journal of Nutrition and Metabolism · doi:10.1007/s12349-011-0051-1
Les lipopolysaccharides bactériens et les maladies métaboliques
Burcelin, R., Chabo, C., Luche, É., Sérino, M., & Corthier, G. (2010) · Cahiers de Nutrition et de Diététique · doi:10.1016/j.cnd.2010.03.001
van Wijck, K. (2013) · Research Publications (Maastricht University) · doi:10.26481/dis.20130704kw
Regulation of TLR9-induced Innate Immune Responses in Sheep Peyer's Patches.
Booth, J. S. (2009) · University Library - University of Saskatchewan (University of Saskatchewan)
Antigen Sampling on the Peyer's Patches in a Murine Small Bowel Transplantation Model
Ping, X., Li, Y., & Li, J. (2010) · Transplantation Proceedings · doi:10.1016/j.transproceed.2010.08.057
Perturbateurs endocriniens et contamination orale : l’intestin oublié
Houdeau, É. (2011) · Médecine & longévité · doi:10.1016/j.mlong.2011.05.001
Speiser, S. (2015) · Universitätsbibliothek der FU Berlin Hochschulschriftenstelle u. Dokumentenserver · doi:10.17169/refubium-17912
Håkansson, Å. (2010) · Lund University Publications (Lund University)
Metadata
- Authors
- Artis, D.
- Affiliations
- University of Pennsylvania (US)
- Corresponding author
- Artis, David
- ORCID
- Artis, David
- Venue
- Nature reviews. Immunology
- Published
- 2008-06
- Volume
- 8
- Issue
- 6
- Pages
- 411-420
- ISSN
- 1474-1733 (ISSN-L)
- 1474-1741
- OpenAlex
- W2025114863
- Cited by
- 1,136
- References
- 167
- Citations by year
- 2026: 27 · 2025: 33 · 2024: 38 · 2023: 55 · 2022: 61 · 2021: 54 · 2020: 51 · 2019: 52 · 2018: 60 · 2017: 56 · 2016: 58 · 2015: 63 · 2014: 92 · 2013: 85 · 2012: 81
- FWCI
- 6.91
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Immunology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Cancer Institute (T32CA009140, T32-CA09140-30)
- National Institute of General Medical Sciences (F31-GM82187, F31GM082187)
- National Institute of Allergy and Infectious Diseases (AI74878, T32AI007532, R01AI074878, F32-AI72943, F32AI072943, R01AI061570, AI 61570)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Keywords
- intestinal epithelial cells, commensal bacteria, immune homeostasis, mucosal immunity, host-microbe interactions, epithelial barrier function, antigen presentation, lymphocytes, pathogen discrimination, gut microbiota
- MeSH terms
- Animals, Bacteria, Gastric Mucosa, Homeostasis, Humans, Intestinal Mucosa
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review