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The gut flora as a forgotten organ
Open accessAbstract
The intestinal microflora is a positive health asset that crucially influences the normal structural and functional development of the mucosal immune system. Mucosal immune responses to resident intestinal microflora require precise control and an immunosensory capacity for distinguishing commensal from pathogenic bacteria. In genetically susceptible individuals, some components of the flora can become a liability and contribute to the pathogenesis of various intestinal disorders, including inflammatory bowel diseases. It follows that manipulation of the flora to enhance the beneficial components represents a promising therapeutic strategy. The flora has a collective metabolic activity equal to a virtual organ within an organ, and the mechanisms underlying the conditioning influence of the bacteria on mucosal homeostasis and immune responses are beginning to be unravelled. An improved understanding of this hidden organ will reveal secrets that are relevant to human health and to several infectious, inflammatory and neoplastic disease processes.
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“In the absence of the resident microbiota, members of the TLR family have low or absent expression profiles in the gut, thus compromising appropriate neuroendocrine responses to pathogenic threats (O'Hara and Shanahan, 2006).”
From The Microbiota-Gut-Brain Axis (2019) · cites this paper as O'Hara and Shanahan, 2006
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“Microbial abundance and community structure in the proximal intestine is affected by gastric acid, pancreaticobiliary secretions, and fast transit45.”
From The gut Microbiome in adult and pediatric functional gastrointestinal disorders (2019) · cites this paper as [45]
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“Studies have since shown that gut bacteria play a vital role in regulating important aspects of brain development and function, along with other host physiology [5, 7].”
From Effect of fecal microbiota transplant on symptoms of psychiatric disorders: a systematic review (2020) · cites this paper as [5]
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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
Recognition of Commensal Microflora by Toll-Like Receptors Is Required for Intestinal Homeostasis
Rakoff-Nahoum, S., Paglino, J., Eslami-Varzaneh, F., Edberg, S., & Medzhitov, R. (2004) · Cell · doi:10.1016/j.cell.2004.07.002 · Cited by 4,251
An Immunomodulatory Molecule of Symbiotic Bacteria Directs Maturation of the Host Immune System
Mazmanian, S. K., Liu, C. H., Tzianabos, A. O., & Kasper, D. L. (2005) · Cell · doi:10.1016/j.cell.2005.05.007 · Cited by 2,910
Rescigno, M., Urbano, M., Valzasina, B., Francolini, M., Rotta, G., Bonasio, R., Granucci, F., Kraehenbuhl, J.-P., & Ricciardi‐Castagnoli, P. (2001) · Nature Immunology · doi:10.1038/86373 · Cited by 2,554
Induction of Protective IgA by Intestinal Dendritic Cells Carrying Commensal Bacteria
Macpherson, A. J., & Uhr, T. (2004) · Science · doi:10.1126/science.1091334 · Cited by 1,584
Gewirtz, A. T., Navas, T. A., Lyons, S., Godowski, P. J., & Madara, J. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.167.4.1882 · Cited by 1,345
Cario, E., & Podolsky, D. K. (2000) · Infection and Immunity · doi:10.1128/iai.68.12.7010-7017.2000 · Cited by 1,245
The ubiquitin-modifying enzyme A20 is required for termination of Toll-like receptor responses
Boone, D. L., Turer, E. E., Lee, E. G., Ahmad, R., Wheeler, M. T., Tsui, C., Hurley, P. J., Chien, M., Chai, S., Hitotsumatsu, O., et al. (2004) · Nature Immunology · doi:10.1038/ni1110 · Cited by 1,104
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- Rook GA, Brunet LR (2005) Microbes, immunoregulation and the gut. Gut 54: 317–320
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Items 201–300 of 1,012
Cerdá, B., Pérez, M., Pérez-Santiago, J. D., Tornero-Aguilera, J. F., González-Soltero, R., & Larrosa, M. (2016) · Frontiers in Physiology · doi:10.3389/fphys.2016.00051 · Cited by 247
Ageing: from inflammation to cancer
Leonardi, G. C., Accardi, G., Monastero, R., Nicoletti, F., & Libra, M. (2018) · Immunity & Ageing · doi:10.1186/s12979-017-0112-5 · Cited by 241
“The bacterial population of the gut microbiota (GM) represents the largest number and concentration of microbes of the human body and it has been demonstrated to take part in many physiological and pathological processes [48, 49].”
BackgroundNutrients Mediate Intestinal Bacteria–Mucosal Immune Crosstalk
Ma, N., Guo, P., Zhang, J., He, T., Kim, S. W., Zhang, G., & Ma, X. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00005 · Cited by 252
Dysbiotic Events in Gut Microbiota: Impact on Human Health
Schippa, S., & Conte, M. (2014) · Nutrients · doi:10.3390/nu6125786 · Cited by 256
The Impact of Probiotic on Gut Health
Collado, M. C., Isolauri, E., Salminen, S., & Sanz, Y. (2009) · Current Drug Metabolism · doi:10.2174/138920009787048437 · Cited by 251
Resveratrol, Metabolic Syndrome, and Gut Microbiota
Chaplin, A. M. L., Carpéné, C., & Mercader, J. (2018) · Nutrients · doi:10.3390/nu10111651 · Cited by 256
Ferrer, M., Ruiz-Rodriguez, A., Lanza, F., Haange, S., Oberbach, A., Till, H., Bargiela, R., Campoy, C., Segura, M. T., Richter, M., et al. (2012) · Environmental Microbiology · doi:10.1111/j.1462-2920.2012.02845.x · Cited by 249
Lazado, C. C., Caipang, C. M. A., & Estante‐Superio, E. G. (2015) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2015.02.023 · Cited by 243
Use of probiotics in gastrointestinal disorders: what to recommend?
Verna, E. C., & Lucak, S. L. (2010) · Therapeutic Advances in Gastroenterology · doi:10.1177/1756283x10373814 · Cited by 248
Possemiers, S., Bolca, S., Verstraete, W., & Heyerick, A. (2010) · Fitoterapia · doi:10.1016/j.fitote.2010.07.012 · Cited by 244
Jin, D., Wu, S., Zhang, Y., Lu, R., Xia, Y., Dong, H. F., & Sun, J. (2015) · Clinical Therapeutics · doi:10.1016/j.clinthera.2015.04.004 · Cited by 236
Yazdankhah, S., Rudi, K., & Bernhoft, A. (2014) · Microbial Ecology in Health & Disease · doi:10.3402/mehd.v25.25862 · Cited by 127
McFarland, L. V. (2014) · BMJ Open · doi:10.1136/bmjopen-2014-005047 · Cited by 235
Gut Microbiota and Their Neuroinflammatory Implications in Alzheimer’s Disease
Giau, V. V., Wu, S., Jamerlan, A., An, S. S. A., Kim, S., & Hulme, J. (2018) · Nutrients · doi:10.3390/nu10111765 · Cited by 239
Yap, I. K. S., Li, J. V., Saric, J., Martin, F., Davies, H., Wang, Y., Wilson, I. D., Nicholson, J. K., Utzinger, J., Marchesi, J. R., et al. (2008) · Journal of Proteome Research · doi:10.1021/pr700864x · Cited by 235
Metabolism of Xenobiotics of Human Environments
Croom, E. L. (2012) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-415813-9.00003-9 · Cited by 258
Challenge to the Intestinal Mucosa During Sepsis
Haußner, F., Chakraborty, S., Halbgebauer, R., & Huber-Lang, M. S. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00891 · Cited by 233
Microbiome disturbances and autism spectrum disorders
Rosenfeld, C. S. (2015) · Drug Metabolism and Disposition · doi:10.1124/dmd.115.063826 · Cited by 229
Vindigni, S. M., Zisman, T. L., Suskind, D. L., & Damman, C. J. (2016) · Therapeutic Advances in Gastroenterology · doi:10.1177/1756283x16644242 · Cited by 241
Gut Microbiota Metabolism and Interaction with Food Components
Vernocchi, P., CHIERICO, F. D., & Putignani, L. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21103688 · Cited by 242
Prebiotic and Probiotic Regulation of Bone Health: Role of the Intestine and its Microbiome
McCabe, L. R., Britton, R. A., & Parameswaran, N. (2015) · Current Osteoporosis Reports · doi:10.1007/s11914-015-0292-x · Cited by 242
Composition of the early intestinal microbiota
Fouhy, F., Ross, R. P., Fitzgerald, G. F., Stanton, C., & Cotter, P. D. (2012) · Gut Microbes · doi:10.4161/gmic.20169 · Cited by 245
Reactive Oxygen Production Induced by the Gut Microbiota: Pharmacotherapeutic Implications
Jones, R. M., Mercante, J. W., & Neish, A. S. (2012) · Current Medicinal Chemistry · doi:10.2174/092986712799828283 · Cited by 232
Lactobacillus fermentumME-3 - an antimicrobial and antioxidative probiotic
Mikelsaar, M., & Zilmer, M. (2009) · Microbial Ecology in Health and Disease · doi:10.1080/08910600902815561 · Cited by 231
Beneficial modulation of the gut microbiota
Walsh, C. J., Guinane, C. M., O'Toole, P. W., & Cotter, P. D. (2014) · FEBS Letters · doi:10.1016/j.febslet.2014.03.035 · Cited by 274
Bile Acid Signaling in Inflammatory Bowel Diseases
Fiorucci, S., Carino, A., Baldoni, M., Santucci, L., Costanzi, E., Graziosi, L., Distrutti, E., & Biagioli, M. (2020) · Digestive Diseases and Sciences · doi:10.1007/s10620-020-06715-3 · Cited by 243
Gut microbiota of healthy and malnourished children in bangladesh
Monira, S., Nakamura, S., Gotoh, K., Izutsu, K., Watanabe, H., Alam, N. H., Endtz, H. P., Cravioto, A., Ali, S. I., Nakaya, T., et al. (2011) · Frontiers in Microbiology · doi:10.3389/fmicb.2011.00228 · Cited by 223
The Central Role of the Gut Microbiota in Chronic Inflammatory Diseases
Ferreira, C. M., Vieira, A. T., Vinolo, M. A. R., Oliveira, F. A., Curi, R., & Martins, F. S. (2014) · Journal of Immunology Research · doi:10.1155/2014/689492 · Cited by 230
Multi-omics data integration considerations and study design for biological systems and disease
Graw, S., Chappell, K., Washam, C. L., Gies, A. J., Bird, J. T., Robeson, M. S., & Byrum, S. D. (2020) · Molecular Omics · doi:10.1039/d0mo00041h · Cited by 231
The Altered Schaedler Flora: Continued Applications of a Defined Murine Microbial Community
Brand, M. W., Wannemuehler, M. J., Phillips, G. J., Proctor, A., Overstreet, A.-M. C., Jergens, A. E., Orcutt, R. P., & Fox, J. G. (2015) · ILAR Journal · doi:10.1093/ilar/ilv012 · Cited by 223
Host-Intestinal Microbiota Mutualism: “Learning on the Fly”
Erkoşar, B., Storelli, G., Defaye, A., & Leulier, F. (2013) · Cell Host & Microbe · doi:10.1016/j.chom.2012.12.004 · Cited by 217
The role of biogeography in shaping diversity of the intestinal microbiota in house mice
Linnenbrink, M., Wang, J., Hardouin, E. A., Künzel, S., Metzler, D., & Baines, J. F. (2013) · Molecular Ecology · doi:10.1111/mec.12206 · Cited by 214
Clarke, G. A., Cryan, J. F., Dinan, T. G., & Quigley, E. M. M. (2012) · Alimentary Pharmacology & Therapeutics · doi:10.1111/j.1365-2036.2011.04965.x · Cited by 221
Albesharat, R., Ehrmann, M. A., Korakli, M., Yazaji, S., & Vogel, R. F. (2011) · Systematic and Applied Microbiology · doi:10.1016/j.syapm.2010.12.001 · Cited by 220
Obesity, diabetes, and the gut microbiome: an updated review
Singer-Englar, T., Barlow, G. M., & Mathur, R. (2018) · Expert Review of Gastroenterology & Hepatology · doi:10.1080/17474124.2019.1543023 · Cited by 224
Fecal microbiota transplantation in disease therapy
Antushevich, H. (2020) · Clinica Chimica Acta · doi:10.1016/j.cca.2019.12.010 · Cited by 224
Epithelial barrier: an interface for the cross‐communication between gut flora and immune system
Goto, Y., & Kiyono, H. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01078.x · Cited by 219
Molecular Modulation of Intestinal Epithelial Barrier: Contribution of Microbiota
Sharma, R. R., Young, C., & Neu, J. (2010) · BioMed Research International · doi:10.1155/2010/305879 · Cited by 220
Ecotoxicology inside the gut: impact of heavy metals on the mouse microbiome
Breton, J., Massart, S., Vandamme, P., De Brandt, E., Pot, B., & Foligné, B. (2013) · BMC Pharmacology and Toxicology · doi:10.1186/2050-6511-14-62 · Cited by 213
The Human Microbiome: From Symbiosis to Pathogenesis
Eloe‐Fadrosh, E. A., & Rasko, D. A. (2013) · Annual Review of Medicine · doi:10.1146/annurev-med-010312-133513 · Cited by 227
Ocejo, M., Oporto, B., & Hurtado, A. (2019) · Scientific Reports · doi:10.1038/s41598-019-39323-x · Cited by 212
The intestinal microbiota and obesity
Kallus, S. J., & Brandt, L. J. (2012) · Journal of Clinical Gastroenterology · doi:10.1097/mcg.0b013e31823711fd · Cited by 210
Gut Dysbiosis in Animals Due to Environmental Chemical Exposures
Rosenfeld, C. S. (2017) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2017.00396 · Cited by 217
Symbiosis and development: The hologenome concept
ROSENBERG, E. B., & Zilber‐Rosenberg, I. (2011) · Birth Defects Research Part C Embryo Today Reviews · doi:10.1002/bdrc.20196 · Cited by 216
The human gut sterolbiome: bile acid-microbiome endocrine aspects and therapeutics
Ridlon, J. M., & Bajaj, J. S. (2015) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2015.01.006 · Cited by 210
Frémont, M., Coomans, D. H., Massart, S., & Meirleir, K. D. (2013) · Anaerobe · doi:10.1016/j.anaerobe.2013.06.002 · Cited by 208
Microbe-host interactions: influence of the gut microbiota on the enteric nervous system
Hyland, N. P., & Cryan, J. F. (2016) · Developmental Biology · doi:10.1016/j.ydbio.2016.06.027 · Cited by 207
Microbial ‘old friends’, immunoregulation and socioeconomic status
Rook, G. A. W., Raison, C. L., & Lowry, C. A. (2014) · Clinical & Experimental Immunology · doi:10.1111/cei.12269 · Cited by 218
Systematic review: microbial dysbiosis and nonalcoholic fatty liver disease
Wieland, A. C., Frank, D. N., Harnke, B., & Bambha, K. M. (2015) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.13376 · Cited by 211
Marzorati, M., Vanhoecke, B. W. A., Ryck, T. D., Sadabad, M. S., Pinheiro, I., Possemiers, S., den Abbeele, P. V., Derycke, L., Bracke, M., Pieters, J., et al. (2014) · BMC Microbiology · doi:10.1186/1471-2180-14-133 · Cited by 208
The human gut virome: a multifaceted majority
Ogilvie, L. A., & Jones, B. V. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.00918 · Cited by 212
Microbiota Signaling Pathways that Influence Neurologic Disease
Cox, L. M., & Weiner, H. L. (2018) · Neurotherapeutics · doi:10.1007/s13311-017-0598-8 · Cited by 210
Interactive relationships between intestinal flora and bile acids
Guo, X., Okpara, E. S., Hu, W., Yan, C., Wang, Y., Liang, Q., Chiang, J. Y. L., & Han, S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23158343 · Cited by 206
Intestinal microbiota is a plastic factor responding to environmental changes
Candela, M., Biagi, E., Maccaferri, S., Turroni, S., & Brigidi, P. (2012) · Trends in Microbiology · doi:10.1016/j.tim.2012.05.003 · Cited by 216
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Rogers, A. W. L., Tsolis, R. M., & Bäumler, A. J. (2020) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00027-19 · Cited by 207
Sasso, J. M., Ammar, R. M., Tenchov, R., Lemmel, S. A., Kelber, O., Grieswelle, M., & Zhou, Q. A. (2023) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.3c00127 · Cited by 229
Ghoshal, U. C., Shukla, R., & Ghoshal, U. (2017) · Gut and Liver · doi:10.5009/gnl16126 · Cited by 218
N-Acetylglucosamine Induces White to Opaque Switching, a Mating Prerequisite in Candida albicans
Huang, G., Song, Y., Sahni, N., Daniels, K. J., Srikantha, T., & Soll, D. R. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1000806 · Cited by 208
Gut Microbiota and Type 2 Diabetes Mellitus: Association, Mechanism, and Translational Applications
Zhang, L., Chu, J., Hao, W., Zhang, J., Li, H., Yang, C., Yang, J., Chen, X., & Wang, H. (2021) · Mediators of Inflammation · doi:10.1155/2021/5110276 · Cited by 228
Nutrient Limitation Governs Staphylococcus aureus Metabolism and Niche Adaptation in the Human Nose
Krismer, B., Liebeke, M., Janek, D., Nega, M., Rautenberg, M., Hornig, G., Unger, C., Weidenmaier, C., Lalk, M., & Peschel, A. (2014) · PLoS Pathogens · doi:10.1371/journal.ppat.1003862 · Cited by 203
Chadchan, S. B., Cheng, M., Parnell, L. A., Yin, Y., Schriefer, A. E., Mysorekar, I. U., & Kommagani, R. (2019) · Human Reproduction · doi:10.1093/humrep/dez041 · Cited by 202
Zhao, C., Yang, C., Wai, S. T. C., Zhang, Y., P. Portillo, M., Paoli, P., Wu, Y., San Cheang, W., Liu, B., Carpéné, C., et al. (2019) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2018.1501658 · Cited by 199
Brain-gut-microbiota axis: challenges for translation in psychiatry
Kelly, J. R., Clarke, G. A., Cryan, J. F., & Dinan, T. G. (2016) · Annals of Epidemiology · doi:10.1016/j.annepidem.2016.02.008 · Cited by 207
The role of the gastrointestinal microbiome in Helicobacter pylori pathogenesis
Sheh, A., & Fox, J. G. (2013) · Gut Microbes · doi:10.4161/gmic.26205 · Cited by 208
Wall, R., Ross, R. P., Shanahan, F., O’Mahony, L., O’Mahony, C., Coakley, M., Hart, O. M., Lawlor, P. G., Quigley, E. M. M., Kiely, B., et al. (2009) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.2008.27023 · Cited by 198
Self-citationTawfick, M. M., Xie, H., Zhao, C., Shao, P., & Farag, M. A. (2022) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2022.03.218 · Cited by 208
Shani-Levi, C., Alvito, P., Andrés, A., Assunção, R., Barberá, R., Blanquet‐Diot, S., Bourlieu‐Lacanal, C., Brodkorb, A., Cilla, A., Deglaire, A., et al. (2016) · Trends in Food Science & Technology · doi:10.1016/j.tifs.2016.10.017 · Cited by 205
Broderick, N. A., Robinson, C. J., McMahon, M. D., Holt, J. F., Handelsman, J., & Raffa, K. F. (2009) · BMC Biology · doi:10.1186/1741-7007-7-11 · Cited by 199
Worms need microbes too: microbiota, health and aging in Caenorhabditis elegans
Cabreiro, F., & Gems, D. (2013) · EMBO Molecular Medicine · doi:10.1002/emmm.201100972 · Cited by 202
Arias, N., Arboleya, S., Allison, J., Kaliszewska, A., Higarza, S. G., Gueimonde, M., & Arias, J. L. (2020) · Nutrients · doi:10.3390/nu12082340 · Cited by 210
d-glutamate and Gut Microbiota in Alzheimer’s Disease
Chang, C.-H., Lin, C.-H., & Lane, H.-Y. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21082676 · Cited by 191
Comparative study on gastrointestinal microbiota of eight fish species with different feeding habits
Li, J., Ni, J., Li, J., Wang, C., Li, X., Wu, S. G., Zhang, T., Yu, Y., & Yan, Q. (2014) · Journal of Applied Microbiology · doi:10.1111/jam.12663 · Cited by 199
Probiotics: How Effective Are They in the Fight against Obesity?
Mazloom, K., Siddiqi, I., & Covașă, M. (2019) · Nutrients · doi:10.3390/nu11020258 · Cited by 210
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Seyoum, Y., Baye, K., & Humblot, C. (2021) · Gut Microbes · doi:10.1080/19490976.2021.1874855 · Cited by 204
Causality of small and large intestinal microbiota in weight regulation and insulin resistance
Scheithauer, T. P. M., Dallinga-Thie, G. M., de Vos, W. M., Nieuwdorp, M., & van Raalte, D. H. (2016) · Molecular Metabolism · doi:10.1016/j.molmet.2016.06.002 · Cited by 188
“tract, and the secretion of anti-bacterial substances such as bile acids [19].”
BackgroundOuter Membrane Vesicles Derived from Escherichia coli Induce Systemic Inflammatory Response Syndrome
Park, K., Choi, K. H., Kim, Y.-S., Hong, B. S., Kim, O. Y., Kim, J. H., Yoon, C. M., Koh, G.-Y., Kim, Y.-K., & Gho, Y. S. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011334 · Cited by 193
Microbiota Modulate Host Gene Expression via MicroRNAs
Dalmasso, G., Nguyen, H. T. T., Yan, Y., Laroui, H., Charania, M. A., Ayyadurai, S., Sitaraman, S. V., & Merlin, D. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019293 · Cited by 200
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Broom, L. J., & Kogut, M. H. (2018) · Veterinary Immunology and Immunopathology · doi:10.1016/j.vetimm.2018.10.002 · Cited by 191
The hygiene hypothesis: current perspectives and future therapies
Stiemsma, L. T., Reynolds, L. A., Turvey, S. E., & Finlay, B. B. (2015) · ImmunoTargets and Therapy · doi:10.2147/itt.s61528 · Cited by 201
Outer Membrane Vesicle-Host Cell Interactions
Cecil, J. D., Sirisaengtaksin, N., O’brien-simpson, N. M., & Krachler, A. M. (2019) · Microbiology Spectrum · doi:10.1128/microbiolspec.psib-0001-2018 · Cited by 198
The role of the intestinal microbiota in enteric infection
Sekirov, I., & Finlay, B. B. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2009.172742 · Cited by 188
Bletz, M. C., Goedbloed, D. J., Sanchez, E., Reinhardt, T., Tebbe, C. C., Bhuju, S., Geffers, R., Jarek, M., Vences, M., & Steinfartz, S. (2016) · Nature Communications · doi:10.1038/ncomms13699 · Cited by 188
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Brink, L., & Lönnerdal, B. L. (2020) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2020.108465 · Cited by 193
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Bell, V., Ferrão, J., Pimentel, L., Pintado, M., & Fernandes, T. (2018) · Foods · doi:10.3390/foods7120195 · Cited by 188
Fang, Z., Li, L., Zhang, H., Zhao, J., Lu, W., & Chen, W. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.720393 · Cited by 200
Modulation of immune homeostasis by commensal bacteria
Ivanov, I. I., & Littman, D. R. (2011) · Current Opinion in Microbiology · doi:10.1016/j.mib.2010.12.003 · Cited by 188
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Mudd, J. C., & Brenchley, J. M. (2016) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiw258 · Cited by 195
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Metadata
- Authors
- O'Hara, A. M., & Shanahan, F.
- Affiliations
- National University of Ireland (IE)
- Corresponding author
- Shanahan, Fergus
- ORCID
- Shanahan, Fergus
- Venue
- The EMBO Reports
- Published
- 2006-07-01
- Volume
- 7
- Issue
- 7
- Pages
- 688-693
- ISSN
- 1469-221X (ISSN-L)
- 1469-3178
- PMC
- PMC1500832
- OpenAlex
- W2117727476
- Cited by
- 2,791
- References
- 54
- Citations by year
- 2026: 67 · 2025: 127 · 2024: 186 · 2023: 174 · 2022: 230 · 2021: 217 · 2020: 243 · 2019: 198 · 2018: 179 · 2017: 184 · 2016: 168 · 2015: 147 · 2014: 123 · 2013: 134 · 2012: 121
- FWCI
- 3.21
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- EMBO Reports (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Science Foundation Ireland
- Alimentary Health
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Life Sciences › Agricultural and Biological Sciences › Food Science › Probiotics and Fermented Foods
- Health Sciences › Medicine › Gastroenterology › Inflammatory Bowel Disease
- Keywords
- gut microbiota, mucosal immunity, inflammatory bowel disease, mucosal homeostasis, bacterial metabolic activity, microbiome manipulation, intestinal disorders, pathogenesis
- MeSH terms
- Animals, Bacteria, Digestive System, Digestive System Diseases, Germ-Free Life, Homeostasis, Humans, Intestinal Mucosa, Models, Biological, Immunity, Mucosal
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