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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.
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“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
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Items 701–800 of 1,000
Inflammatory Bowel Diseases and Enteric Microbiota
Kim, J. M. (2010) · Korean Journal of Gastroenterology · doi:10.4166/kjg.2010.55.1.4 · Cited by 11
Phasic study of intestinal homeostasis disruption in experimental intestinal obstruction
Yu, X. (2014) · World Journal of Gastroenterology · doi:10.3748/wjg.v20.i25.8130 · Cited by 12
Immunopathology and Immunomodulation
Metodiev, K. (2015) · InTech eBooks · doi:10.5772/59217 · Cited by 12
Belogortseva, N., Krezalek, M. A., Guyton, K. L., Labno, C. M., Poroyko, V. A., Zaborina, O. Y., & Alverdy, J. C. (2017) · PLoS ONE · doi:10.1371/journal.pone.0182825 · Cited by 12
Protecting Intestinal Microenvironment Alleviates Acute Graft-Versus-Host Disease
Zhou, Z., Shang, T., Li, X., Zhu, H., Qi, Y., Zhao, X., Chen, X., Shi, Z., Pan, G., Wang, Y., et al. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2020.608279 · Cited by 12
“Intestinal epithelial cells play a cardinal role in maintaining intestinal microenvironment (Artis, 2008).”
BackgroundGut Microbiota and Immunity: Possible Role in Sudden Infant Death Syndrome
Goldwater, P. N. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00269 · Cited by 15
Molecular Biology of the Host-Microbe Interaction in Periodontal Diseases
Rossa, C., & Kirkwood, K. L. (2012) · Elsevier eBooks · doi:10.1016/b978-1-4377-0416-7.00025-1 · Cited by 13
Lee, J., Jang, A., Kim, J. W., Han, J. H., Chun, B. H., Jung, H. S., Jeon, C. O., & Myung, S. C. (2017) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-017-9286-6 · Cited by 12
“The human vagina continuously responds to immunologically unique conditions in which an efficient antimicrobial defense system is required to eliminate potential pathogens, while tolerating beneficial commensal microbes [4, 5].”
BackgroundFadaee, M., Mahrooghi, D., Lahouty, M., Oskouie, S. A., & Nezhadi, J. (2025) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2025.105837 · Cited by 13
PTPN2 Is a Critical Regulator of Ileal Paneth Cell Viability and Function in Mice
Canale, V., Spalinger, M. R., Alvarez, R., Sayoc-Becerra, A., Sanati, G., Manz, S., Chatterjee, P., Santos, A. N., Lei, H., Jahng, S., et al. (2023) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2023.03.009 · Cited by 12
Comparison of gut microbiota dysbiosis between pemphigus vulgaris and bullous pemphigoid
Han, Z., Fan, Y., Wu, Q., Guo, F., Li, S., Hu, X., & Zuo, Y. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2023.111470 · Cited by 11
Wang, Y., Gao, Y., Feng, J., & Dou, Y. (2020) · Chinese Journal of Integrative Medicine · doi:10.1007/s11655-020-3261-x · Cited by 11
Is Regular Probiotic Practice Safe for Management of Sepsis?
Kumar, R., Tripathi, A. S., Sharma, N., Singh, G., & Mohapatra, L. (2021) · Chinese Journal of Integrative Medicine · doi:10.1007/s11655-021-3334-5 · Cited by 11
Meng, T., Liu, C., Chen, Y., Yu, M., He, J., Tan, B., Fu, X., He, J., & Xiao, D. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.111153 · Cited by 11
Wang, C.-W., Chang, W.-L., Huang, Y.-C., Chou, F.-P., Chan, F., Su, S.-C., Huang, S., Ko, H.-H., Ko, Y.-L., Lin, H.-C., et al. (2015) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2015.04.006 · Cited by 11
Dead Bacteria Reverse Antibiotic-Induced Host Defense Impairment in Burns
Chen, L.-W., Chen, P.-H., Fung, C.-P., & Hsu, C.-M. (2014) · Journal of the American College of Surgeons · doi:10.1016/j.jamcollsurg.2014.04.016 · Cited by 11
“The intestinal tract acts as a major physical barrier between the microflora and internal host tissue and responds to the mucosal innate system through the commensal microflora (29).”
BackgroundImmunomodulatory effects ofClostridium butyricumon human enterocyte-like HT-29 cells
Quanxin, G., Li-li, Q., Tian-xing, W., Tingting, X., & Jinbo, W. (2013) · Animal Cells and Systems · doi:10.1080/19768354.2013.789075 · Cited by 11
“2006; Artis 2008).”
“Oral Vaccine Antigen Induced Immune Response Signalling Pathways: Current and Future Perspectives”
Dev, A. (2014) · Journal of Vaccines & Vaccination · doi:10.4172/2157-7560.1000225 · Cited by 11
“These highly specialised M cells have some unique structural and functional features which facilitate endocytosis and transport of macromolecules and bacteria as shown in Figure 1 [40,41].”
BackgroundZou, Z., Zuo, D., Yang, J., & Fan, H. J. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.07.066 · Cited by 11
Effects of synbiotics on intestinal mucosal barrier in rat model
Xue, Z., Yu, J., Zhao, M., Kang, W., & Ma, Z. (2017) · Clinical Nutrition Experimental · doi:10.1016/j.yclnex.2017.02.001 · Cited by 11
Adaptative responses of myenteric neurons of Sphoeroides testudineus to environmental pollution
Gonçalves, A. R. N., Marinsek, G. P., Abessa, D. M. D. S., & Mari, R. D. B. (2019) · NeuroToxicology · doi:10.1016/j.neuro.2019.10.008 · Cited by 11
Samarasinghe, M. B., Sehested, J., Larsen, T., & Hernández-Castellano, L. E. (2020) · Journal of Dairy Science · doi:10.3168/jds.2019-17404 · Cited by 11
Abramson, S. L. (2012) · PEDIATRICS · doi:10.1542/peds.2012-2183cccc · Cited by 11
Ahmad, A. A. M., Elmowalid, G. A., Abdelhamid, A. E.-S., Mohammad, A. A. E., & Abdelwahab, A. M. O. (2023) · BMC Veterinary Research · doi:10.1186/s12917-023-03632-1 · Cited by 10
“The mucins layer serves as a physical barrier between the lumen and epithelium that is continually exposed to microbial pathogens [55, 56], confirming the efficacy of the tested nanoparticles in providing mucosal protection.”
BackgroundRole of IL-33/ST2 Pathway in Inflammatory Bowel Disease: An Overview and Future Perspectives
Giordano, W. G., Ricciardi, G., Casciaro, M., Fiorentino, V., Pizzimenti, C., Viola, A., Martini, M., Tuccari, G., & Ieni, A. (2024) · Gastrointestinal Disorders · doi:10.3390/gidisord6020030 · Cited by 9
“…injury, IL-33 release stimulates immune responses via ST2-expressing cells, Myo fi broblasts in intestinal tissue serve as an IL-33 source in IBD, and mast cell-mediated in fl ammation may drive fi broblast proliferation towards fi brogenesis [27]. potentially reducing inflammation severity [31,69].”
BackgroundHidalgo-Cantabrana, C., Kekkonen, R. A., Reyes‐Gavilán, C. G. D. L., Salminen, S., Korpela, R., Gueimonde, M., & Ruas‐Madiedo, P. (2013) · Journal of Functional Foods · doi:10.1016/j.jff.2013.11.001 · Cited by 10
Cerrillo, E., Moret, I., Iborra, M., Ramos, D., Busó, E. J., Tortosa, L., González, E. S., Nos, P., & Beltrán, B. (2017) · Clinical & Experimental Immunology · doi:10.1111/cei.13085 · Cited by 10
Rajković, E., Schwarz, C., Kapsamer, S. B., Schedle, K., Reisinger, N., Emsenhuber, C., Oceľová, V., Roth, N., Frieten, D., Dusel, G., et al. (2022) · Antioxidants · doi:10.3390/antiox11081428 · Cited by 10
“However, epithelial mucosal cells are not a simple physical barrier, and they play a notable role in a variety of immune functions [9,17].”
BackgroundLiu, J., Ren, H., Yuan, F., Shao, M., & Luo, H.-S. (2022) · PeerJ · doi:10.7717/peerj.14390 · Cited by 10
“The gut microbiota has a significant impact on intestinal homeostasis (Artis, 2008).”
BackgroundVulcano, A. B., Tino‐De‐Franco, M., Amaral, J. A., Ribeiro, O. G., Cabrera, W. H. K., Bordenalli, M. A., Carbonare, C. B., Álvares, E. P., & Carbonare, S. B. (2014) · Microbiology and Immunology · doi:10.1111/1348-0421.12153 · Cited by 10
“This decline may have been caused by rapid elimination of the bacteria through natural intestinal transit and gut mucosal physiological defense mechanisms (20).”
BackgroundA20 inhibits lipopolysaccharide-induced inflammation in enterocytes
Zheng, C., Shi, J., Huang, Y., & Wang, S. (2016) · World Journal of Gastrointestinal Pharmacology and Therapeutics · doi:10.4292/wjgpt.v7.i4.540 · Cited by 10
Self-reactive B cells in the GALT are actively curtailed to prevent gut inflammation
Shukla, A., Chen, C., Jellusova, J., Leung, C. R., Kao, E., Bhat, N., Lin, W., Apgar, J. R., & Rickert, R. C. (2019) · JCI Insight · doi:10.1172/jci.insight.130621 · Cited by 10
Kumar, S., V, Patial, M., & Sharma, R. K. (2020) · Springer eBooks · doi:10.1007/978-3-030-41866-3_13 · Cited by 10
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) · Diabetology & Metabolic Syndrome · doi:10.1186/s13098-022-00954-2 · Cited by 14
“These also activate the release of mucin by goblet epithelial cells, forming a glycocalyx that breaks down a physical and antibacterial barrier [39].”
BackgroundMicrocystin-LR exposure interfered maintenance of colonic microenvironmental homeostasis in rat
Liu, Y., Qi, C., Li, D., Li, R.-M., Li, R.-M., & Yang, W. (2023) · Food and Chemical Toxicology · doi:10.1016/j.fct.2023.113611 · Cited by 10
Kang, S., Jeon, J. H., Woo, S., Yang, J. S., Kim, K. W., Yun, C., & Han, S. H. (2012) · Comparative Immunology Microbiology and Infectious Diseases · doi:10.1016/j.cimid.2012.02.003 · Cited by 10
Butyrate regulation of distinct macrophage subsets: Opposing effects on M1 and M2 macrophages
Foey, A. (2011) · PEARL (University of Plymouth) · Cited by 10
Role of Sam68 as an adaptor protein in inflammatory signaling
Gowd, V., Kass, J. D. A., Sarkar, N., & Ramakrishnan, P. (2024) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-023-05108-9 · Cited by 9
“The intestinal epithelial cells (IEC) regulate intestinal homeostasis by participating in coordinated responses to signals from the microbiota and local leukocyte populations [74, 75].”
BackgroundA Comprehensive Review on Health Benefits of Fructooligosaccharides
Atta, A., Sharif, S., Haroon, K., Rasheed, M., Menon, S. V., Balaji, J., Jain, B., Jameel, Q. Y., & Shah, M. A. (2025) · eFood · doi:10.1002/efd2.70041 · Cited by 9
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Chen, J. W., Xu, Y., & Cao, P. (2025) · Physiology · doi:10.1152/physiol.00016.2025 · Cited by 13
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Zaph, C. (2010) · Journal of Clinical Investigation · doi:10.1172/jci45263 · Cited by 9
Liu, C., Qi, X., Guan, K., Chen, H., Li, Q., Mao, K., Shen, G., & Ma, Y. (2024) · Journal of Functional Foods · doi:10.1016/j.jff.2024.106048 · Cited by 9
Silva-Guillen, Y. V., Arellano, C., Wiegert, J., Boyd, R. D., Padilla, G. E. M., & van Heugten, E. (2024) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-023-00981-7 · Cited by 11
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BackgroundThe Genetic Predisposition and the Interplay of Host Genetics and Gut Microbiome in Crohn Disease
Jian-zhong, H. (2014) · Clinics in Laboratory Medicine · doi:10.1016/j.cll.2014.08.003 · Cited by 9
“Commensal bacteria also promote angiogenesis and development of the intestinal epithelium and have been shown to be essential for the normal development and function of the immune system.(29) Although miniscule inoculations of”
Nizza, S., Rando, F., Fiorito, F., Pagnini, U., Iovane, G., & Martino, L. D. (2014) · Research in Veterinary Science · doi:10.1016/j.rvsc.2014.03.015 · Cited by 9
Fung, Q. M., & Szilagyi, A. (2012) · International Journal of Inflammation · doi:10.1155/2012/493717 · Cited by 9
Corsetti, G., Romano, C., Pasini, E., Testa, C., & Dioguardi, F. (2021) · Nutrients · doi:10.3390/nu13041089 · Cited by 9
“Intestinal microbiota is believed to regulate the level of NF-κB activity at the epithelial interface and thereby affects the mucosal immune balance [53,54].”
BackgroundSharma, R. R., Young, C., Mshvildadze, M., & Neu, J. (2009) · NeoReviews · doi:10.1542/neo.10-4-e166 · Cited by 9
Tian, Z., Yang, L., Li, P., Xiao, Y., Peng, J., Wang, X., Li, Z., Liu, M., Bi, D., & Shi, D. (2016) · Animal Cells and Systems · doi:10.1080/19768354.2016.1160955 · Cited by 11
“results proved that some probiotics could regulate IECs to avoid an acute inflammatory response to intestinal pathogen by expressing a variety of anti-inflammatory cytokines (Artis 2008).”
BackgroundResultUnraveling the dose-response puzzle of L. monocytogenes: A mechanistic approach
Rahman, A., Munther, D. S., Fazil, A., Smith, B. A., & Wu, J. (2016) · Infectious Disease Modelling · doi:10.1016/j.idm.2016.09.001 · Cited by 9
“Both T cells and B cells retain memories which can promptly clear a possible secondary infection (Artis, 2008; Pamer, 2004).”
BackgroundNovel regulatory Th17 cells and regulatory B cells in modulating autoimmune diseases
Singh, B., Summers, K. L., & Kerfoot, S. M. (2018) · Cellular Immunology · doi:10.1016/j.cellimm.2018.09.002 · Cited by 10
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Thornton, C. A., & Morgan, G. (2009) · Nestlé Nutrition Institute Workshop series · doi:10.1159/000235782 · Cited by 9
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Söderholm, J. D. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-382026-6.00074-9 · Cited by 10
On the mechanism of antibiotic resistance and fecal microbiota transplantation
Kang, X., Yan, J., Huang, F., & Yang, L. (2019) · Mathematical Biosciences & Engineering · doi:10.3934/mbe.2019354 · Cited by 8
Ramos, N. L., Lamprokostopoulou, A., Chapman, T. A., Chin, J. J.-C., Römling, U., Brauner, A., & Katouli, M. (2010) · Microbial Pathogenesis · doi:10.1016/j.micpath.2010.11.003 · Cited by 8
Schümann, M., Winter, S., Wichner, K., May, C., Kühl, A. A., Batra, A., Siegmund, B., Zeitz, M., Schulzke, J.-D., Lipp, M., et al. (2012) · Mucosal Immunology · doi:10.1038/mi.2012.15 · Cited by 8
Common Presentations and Diagnostic Approaches
Rezaei, N., de Vries, E., Gambineri, E., & Haddad, É. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-405546-9.00001-7 · Cited by 8
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Liu, Z., Cominelli, F., Martino, L. D., Liu, R., Devireddy, N., Devireddy, L. R., & Wald, D. N. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00812 · Cited by 8
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BackgroundDiao, H., Xiao, Y., Yan, H., Yu, B., He, J., Zheng, P., Yu, J., Mao, X., & Chen, D. (2021) · BioMed Research International · doi:10.1155/2021/9823969 · Cited by 8
“(ZO family) and transmembrane protein (occludin and claudin families), which participate in the formation of the intestinal mucosal barrier and play a decisive role in the intestinal barrier [46].”
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Jin, H., Che, S., Wu, K., & Wu, M. (2022) · Food & Function · doi:10.1039/d2fo01512a · Cited by 8
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Samanta, S. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-85730-7.00023-0 · Cited by 8
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Hermon-Taylor, J. (2009) · Gut Pathogens · doi:10.1186/1757-4749-1-3 · Cited by 8
“with epithelial cells particularly through Toll-like receptors ensures the proper post-natal maturation of the gut, stimulation of innate immune defences, the development of Peyer's patches and IgA production, angiogenesis, the education of the adaptive immune system and development of immunological tolerance [10,11].”
BackgroundKristek, M., Collins, L. E., DeCourcey, J., McEvoy, F., & Loscher, C. E. (2014) · Innate Immunity · doi:10.1177/1753425914538294 · Cited by 8
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Alam, M., Abedi, V., Bassaganya-Riera, J., Wendelsdorf, K. V., Bisset, K. R., Deng, X., Eubank, S., Hontecillas, R., Hoops, S., & MARATHE, M. V. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-803697-6.00006-0 · Cited by 8
Balfe, Á., Lennon, G., Lavelle, A., Docherty, N. G., Coffey, J. C., Sheahan, K. D., Winter, D. C., & O’Connell, P. R. (2018) · Clinical and Experimental Gastroenterology · doi:10.2147/ceg.s145224 · Cited by 8
“IECs play an important role in colonic homeostasis and are considered to be deregulated in a number of colonic conditions.(1) The panel of genes chosen for gene expression analysis was based on known functions of epithelial cells including mucus gel layer (MGL) and defensin secretions, responses to lipopolysaccharides…”
InfluentialLakhdari, O., Cultrone, A., Tap, J., Gloux, K., Bernard, F., Ehrlich, S. D., Lefèvre, F., Dore, J. M., & Blottière, H. M. (2010) · PLoS ONE · doi:10.1371/annotation/4ea12169-7c97-497c-a45f-52203543065f · Cited by 8
Yoon, D. H., Kim, J. Y., Keon, H., Lee, H. G., Seo, K., Shim, J.-J., Lee, J.-L., & Kim, H. (2024) · Journal of Agriculture and Food Research · doi:10.1016/j.jafr.2024.100965 · Cited by 9
Oliveira, I. C. C. S., Marinsek, G. P., Correia, L. V. B., da Silva, R. C. B., Castro, Í. B., & Mari, R. D. B. (2024) · Autonomic Neuroscience · doi:10.1016/j.autneu.2024.103176 · Cited by 8
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“…the physiological and immunological gut aspects of the development of oral cancer vaccines and critically analyses the current strategies leading to new hopes for their clinical application [16]. as a framework for support, the muscularis aids in movement, and the serosa covers the gut [22,23].”
BackgroundGuo, F., Liu, H., Li, X., Hu, Z., Huang, J., Bi, R., Abbas, W., Guo, Y., & Wang, Z. (2023) · Antioxidants · doi:10.3390/antiox13010048 · Cited by 7
“…of nutrients and fluids simultaneously, and plays a crucial role in separating the host’s internal milieu from the external environment and preventing the transport of potentially harmful substances from entering the underlying tissue, including luminal microbes and antigenic molecules [2,3].”
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Xu, R., Gu, C., Wang, X., Zou, D., Wang, T., Chang, H., He, X., Huang, K., Liu, J., & Wang, D. (2025) · Journal of Experimental Biology · doi:10.1242/jeb.250060 · Cited by 7
Lukichev, B. G., Rumyantsev, A. S., Panina, I. Y., & Акименко, В. Б. (2019) · Nephrology (Saint-Petersburg) · doi:10.24884/1561-6274-2018-23-1-18-31 · Cited by 9
“Пробиотики также могут модулировать активацию провоспалительного ядерного фактора κB для предотвращения утечки липополисахарида и уменьшения секреции интерлейкина-8, который является мощным хемоаттрактантом нейтрофилов в местах повреждения кишечника [71].”
Ramirez, M., Pell, N., Mejías, M., & Fernández, M. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-11093-2_5 · Cited by 7
Assessing the efficacy of antibiotic treatment to produce earthworms with a suppressed microbiome
Omosigho, H. O., Swart, E., Sizmur, T. P., Spurgeon, D. J., Svendsen, C., & Shaw, L. J. (2021) · European Journal of Soil Biology · doi:10.1016/j.ejsobi.2021.103366 · Cited by 7
Wang, B., Chen, J., Wang, S., Zhao, X., Lu, G., & Tang, X. (2017) · Beneficial Microbes · doi:10.3920/bm2016.0019 · Cited by 7
Amino Acids and Immune Functions
Tan, B., Xie, M., & Yin, Y. (2013) · Springer eBooks · doi:10.1007/978-3-7091-1328-8_12 · Cited by 7
Review: Postnatal development of the mucosal immune system and consequences on health in adulthood
Lewis, M. C., Inman, C. F., & Bailey, M. (2010) · Canadian Journal of Animal Science · doi:10.4141/cjas09112 · Cited by 7
Maintaining Diplomatic Relations Between Mammals and Beneficial Microbial Communities
Hill, D. A., & Artis, D. (2009) · Science Signaling · doi:10.1126/scisignal.298pe77 · Cited by 7
The Role of Mucosal Immunity: What Can We Learn From Animal and Human Studies?
Gleeson, P. J., & Monteiro, R. C. (2024) · Seminars in Nephrology · doi:10.1016/j.semnephrol.2025.151566 · Cited by 6
Xu, Y., Tao, Y., Pan, H., Wang, Z., Wang, H., & Luo, Q. (2025) · Frontiers in Bioscience-Landmark · doi:10.31083/fbl41531 · Cited by 6
Colectomy in an ICU patient population : clinical and histological evaluation
Sipola, S. (2014) · Cited by 6
Host-parasite interactions in infections due to Entamoeba histolytica
Singh, A., & Banerjee, T. (2022) · Tropical parasitology · doi:10.4103/tp.tp_81_21 · Cited by 6
“[34] The existence of the parasite in the host requires interactions in favor of the parasite with the intestinal compartments, thus allowing its survival.”
Mallick, K., Islam, S. R., Krishna, V., Manna, S. K., & Banerjee, S. (2025) · Life Sciences · doi:10.1016/j.lfs.2025.123392 · Cited by 6
Lim, J.-H., Na, G., & Kang, J. (2025) · Food Hydrocolloids · doi:10.1016/j.foodhyd.2025.111469 · Cited by 8
The stimulatory effect of fusobacteria on dendritic cells under aerobic or anaerobic conditions
Koido, S., Horiuchi, S., Kan, S., Bito, T., Ito, Z., Uchiyama, K., Saruta, M., Sato, N., & Ohkusa, T. (2022) · Scientific Reports · doi:10.1038/s41598-022-14934-z · Cited by 6
Comparative analysis of intestinal flora between rare wild red-crowned crane and white-naped crane
Gao, Z., Song, H., Dong, H., Ji, X., Lei, Z., Tian, Y., Wu, Y., & Zou, H. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.1007884 · Cited by 6
“Lactobacillus inhibits the growth of pathogenic microorganisms, enhances the barrier function of intestinal epithelial cells, reduces inflammation, and enhances the body’s immune capacity (Artis, 2008; Milani et al., 2017).”
BackgroundMa, X., Li, J., Yang, L., Liu, H., Zhu, Y., Ren, H., Yu, F. W., & Liu, B. (2023) · Veterinary Sciences · doi:10.3390/vetsci10020169 · Cited by 6
“Thus, it is evident that changes in the gut microbiota have effects on the course of many diseases and affect host homeostasis and immune function [4,5,8].”
BackgroundEffects of rifaximin on indomethacin-induced intestinal damage in guinea-pigs.
Ciobanu, L., Taulescu, M. A., Prundus, R., Diaconu, B., Andreica, V., Cătoi, C., Pascu, O., & Tantau, M. V. (2014) · PubMed · Cited by 6
Tsay, T.-B., Yang, M.-C., Sun, J., Chen, P.-H., Lin, Y., Shih, M.-H., & Chen, L.-W. (2016) · Formosan Journal of Surgery · doi:10.1016/j.fjs.2016.04.007 · Cited by 6
Yokoyama, N., Ohta, H., Kagawa, Y., Nagata, N., Nisa, K., Morita, T., Osuga, T., Sasaki, N., Morishita, K., Nakamura, K., et al. (2017) · Veterinary Immunology and Immunopathology · doi:10.1016/j.vetimm.2017.05.006 · Cited by 6
Innate and Mucosal Immunity in the Developing Gastrointestinal Tract
McElroy, S. J., Frey, M. R., Torres, B. A., & Maheshwari, A. (2018) · Elsevier eBooks · doi:10.1016/b978-0-323-40139-5.00072-3 · Cited by 6
Typography, Morphology, and Syntax Characteristics of Texting
Haryono, H., Lelono, B., & Kholifah, A. N. (2018) · Lingua Cultura · doi:10.21512/lc.v12i2.3976 · Cited by 6
The Role of ST2 Receptor in the Regulation of Brucella abortus Oral Infection
Santos, R. A., Campos, P. C., Rungue, M., Rocha, V., Santos, D., de Almeida, V. M., Marinho, F. V., Martins, F. S., Ricci, M. F., dos Reis, D. C., et al. (2020) · Pathogens · doi:10.3390/pathogens9050328 · Cited by 6
Bescucci, D. M., Clarke, S. T., Brown, C. L. J., Boras, V. F., Montina, T., Uwiera, R. R. E., & Inglis, G. D. (2020) · Gut Pathogens · doi:10.1186/s13099-020-00386-1 · Cited by 6
Innate Immunity and Inflammation
McKarns, S. C. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.64228-9 · Cited by 6
Common presentations and diagnostic approaches
Rezaei, N., de Vries, E., Gambineri, E., Meyts, I., & Haddad, É. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-816768-7.00001-6 · Cited by 5
Effects of the non-commensal Methylococcus capsulatus Bath on mammalian immune cells
Christoffersen, T. E., Hult, L. T. O., Solberg, H., Bakke, A. M., Kuczkowska, K., Huseby, E. C., Jacobsen, M., Lea, T., & Kleiveland, C. R. (2015) · Molecular Immunology · doi:10.1016/j.molimm.2015.02.019 · Cited by 6
Microorganisms Responsible for Neonatal Diarrhea
O’Ryan, M. L., Nataro, J. P., & Cleary, T. G. (2010) · Elsevier eBooks · doi:10.1016/b978-1-4160-6400-8.00011-0 · Cited by 6
“The intestinal epithelium serves as a nutrient absorptive machine, barrier to pathogen entry, regulator of inflammation, and critical element in maintaining immune homeostasis of the gut [19,42].”
BackgroundGudi, C. R., Wannemuehler, M. J., & Mansell, T. J. (2025) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2025.115650 · Cited by 5
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
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