The role of gut microbiota in immune homeostasis and autoimmunity

A core gut microbiome in obese and lean twins

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The human microbiome project

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Impact of diet in shaping gut microbiota revealed by a comparative study in children from Europe and rural Africa

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Host-Bacterial Mutualism in the Human Intestine

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Delivery mode shapes the acquisition and structure of the initial microbiota across multiple body habitats in newborns

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Molecular-phylogenetic characterization of microbial community imbalances in human inflammatory bowel diseases

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Induction of Intestinal Th17 Cells by Segmented Filamentous Bacteria

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Recognition of Commensal Microflora by Toll-Like Receptors Is Required for Intestinal Homeostasis

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Induction of Colonic Regulatory T Cells by Indigenous <i>Clostridium</i> Species

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Ecological and Evolutionary Forces Shaping Microbial Diversity in the Human Intestine

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Regulation of inflammatory responses by gut microbiota and chemoattractant receptor GPR43

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The Effect of Diet on the Human Gut Microbiome: A Metagenomic Analysis in Humanized Gnotobiotic Mice

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Topographical and Temporal Diversity of the Human Skin Microbiome

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An Immunomodulatory Molecule of Symbiotic Bacteria Directs Maturation of the Host Immune System

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Development of the Human Infant Intestinal Microbiota

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The effect of infections on susceptibility to autoimmune and allergic diseases.

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Projection of an Immunological Self Shadow Within the Thymus by the Aire Protein

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A microbial symbiosis factor prevents intestinal inflammatory disease

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Reduced diversity of faecal microbiota in Crohn’s disease revealed by a metagenomic approach

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Factors influencing the composition of the intestinal microbiota in early infancy

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NLRP6 Inflammasome Regulates Colonic Microbial Ecology and Risk for Colitis

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Innate immunity and intestinal microbiota in the development of Type 1 diabetes

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Worlds within worlds: evolution of the vertebrate gut microbiota

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The Toll-like receptor 2 pathway establishes colonization by a commensal of the human microbiota

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Gut-Residing Segmented Filamentous Bacteria Drive Autoimmune Arthritis via T Helper 17 Cells

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Resident Enteric Bacteria Are Necessary for Development of Spontaneous Colitis and Immune System Activation in Interleukin-10-Deficient Mice

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The Key Role of Segmented Filamentous Bacteria in the Coordinated Maturation of Gut Helper T Cell Responses

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Analysis of Intestinal Flora Development in Breast-Fed and Formula-Fed Infants by Using Molecular Identification and Detection Methods

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Proinflammatory T-cell responses to gut microbiota promote experimental autoimmune encephalomyelitis

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Recognition of peptidoglycan from the microbiota by Nod1 enhances systemic innate immunity

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Microbial Flora Drives Interleukin 22 Production in Intestinal NKp46+ Cells that Provide Innate Mucosal Immune Defense

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ATP drives lamina propria TH17 cell differentiation

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Salmonella enterica serovar typhimurium exploits inflammation to compete with the intestinal microbiota

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Peripheral education of the immune system by colonic commensal microbiota

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Commensal anaerobic gut bacteria attenuate inflammation by regulating nuclear-cytoplasmic shuttling of PPAR-γ and RelA

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Human intestinal macrophages display profound inflammatory anergy despite avid phagocytic and bacteriocidal activity

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Communicable Ulcerative Colitis Induced by T-bet Deficiency in the Innate Immune System

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RORγt and commensal microflora are required for the differentiation of mucosal interleukin 22–producing NKp46+ cells

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Reversible Microbial Colonization of Germ-Free Mice Reveals the Dynamics of IgA Immune Responses

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Use of axenic animals in studying the adaptation of mammals to their commensal intestinal microbiota

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Enterobacteriaceae Act in Concert with the Gut Microbiota to Induce Spontaneous and Maternally Transmitted Colitis

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Cellular and genetic mechanisms of self tolerance and autoimmunity

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The Microbial Ecology of the Large Bowel of Breastfed and Formula-fed Infants During the First Year of Life

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Role of Gut Commensal Microflora in the Development of Experimental Autoimmune Encephalomyelitis

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Intestinal Bacteria and the Regulation of Immune Cell Homeostasis

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A polysaccharide from the human commensal Bacteroides fragilis protects against CNS demyelinating disease

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Commensal DNA Limits Regulatory T Cell Conversion and Is a Natural Adjuvant of Intestinal Immune Responses

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Antibiotic-Induced Perturbations of the Intestinal Microbiota Alter Host Susceptibility to Enteric Infection

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A Novel Probiotic Mixture Exerts a Therapeutic Effect on Experimental Autoimmune Encephalomyelitis Mediated by IL-10 Producing Regulatory T Cells

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Specificities of the fecal microbiota in inflammatory bowel disease

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The Incidence of Type-1 Diabetes in NOD Mice Is Modulated by Restricted Flora Not Germ-Free Conditions

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Induction of a regulatory B cell population in experimental allergic encephalomyelitis by alteration of the gut commensal microflora

Ochoa-Repáraz, J., Mielcarz, D., Haque-Begum, S., & Kasper, L. (2010) · Gut microbes · doi:10.4161/gmic.1.2.11515 · Cited by 142 · see citing works

Commensal Microbiota and CD8+ T Cells Shape the Formation of Invariant NKT Cells

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Effects of a germ-free environment on gut immune regulation and diabetes progression in non-obese diabetic (NOD) mice

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The Role of Environmental Antigens in the Spontaneous Development of Autoimmunity in MRL- lpr Mice

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Mode of Delivery Is Associated With Asthma and Allergy Occurrences in Children

Salam, M. T., Margolis, H. G., McConnell, R., McGregor, J., Avol, E., & Gilliland, F. D. (2005) · Annals of Epidemiology · doi:10.1016/j.annepidem.2005.06.054 · Cited by 117 · see citing works

Antibiotics and probiotics in treatment of inflammatory bowel disease

Gionchetti, P. (2006) · World Journal of Gastroenterology · doi:10.3748/wjg.v12.i21.3306 · Cited by 113 · see citing works

Defective Differentiation of Regulatory FoxP3+ T Cells by Small-Intestinal Dendritic Cells in Patients With Type 1 Diabetes

Badami, E., Sorini, C., Coccia, M., Usuelli, V., Molteni, L., Bolla, A. M., Scavini, M., Mariani, A., King, C., Bosi, E., et al. (2011) · Diabetes · doi:10.2337/db10-1201 · Cited by 113 · see citing works

Proliferative recruitment of intestinal intraepithelial lymphocytes after microbial colonization of germ‐free mice

Imaoka, A., Matsumoto, S., Setoyama, H., Okada, Y., & Umesaki, Y. (1996) · European Journal of Immunology · doi:10.1002/eji.1830260434 · Cited by 106 · see citing works

Effects of microflora on the neonatal development of gut mucosal T cells and myeloid cells in the mouse

Williams, A. M., Probert, C. S., Štëpánková, R., Tlaskalová‐Hogenová, H., Phillips, A. C., & Bland, P. W. (2006) · Immunology · doi:10.1111/j.1365-2567.2006.02458.x · Cited by 98 · see citing works

Cesarean delivery is associated with celiac disease but not inflammatory bowel disease in children

Decker, E., Hornef, M. W., & Stockinger, S. (2011) · Gut Microbes · doi:10.4161/gmic.2.2.15414 · Cited by 95 · see citing works

The Lifestyle of the Segmented Filamentous Bacterium: A Non-Culturable Gut-Associated Immunostimulating Microbe Inferred by Whole-Genome Sequencing

Kuwahara, T., Ogura, Y., Oshima, K., et al. (2011) · DNA Research · doi:10.1093/dnares/dsr022 · Cited by 95 · see citing works

Immune-deficient animals in biomedical research

Rygaard, J., Brunner, N. A., Groem, N., & Spang‐Thomsen, M. (1987) · Medical Entomology and Zoology · Cited by 94 · see citing works

Danger-free autoimmune disease in Aire-deficient mice

Gray, D. H. D., Gavanescu, I., Benoist, C. O., & Mathis, D. J. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0709160104 · Cited by 84 · see citing works

SMALL INTESTINAL MUCOSAL CELL PROLIFERATION AND BACTERIAL FLORA IN THE CONVENTIONALIZATION OF THE GERMFREE MOUSE

Khoury, K. A., Floch, M. H., & Hersh, T. (1969) · The Journal of Experimental Medicine · doi:10.1084/jem.130.3.659 · Cited by 78 · see citing works

Epidemiology of type 1 diabetes and what animal models teach us about the role of viruses in disease mechanisms

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The functions of mucosal T cells in containing the indigenous commensal flora of the intestine

Macpherson, A. J., Martinic, M. M. A., & Harris, N. L. (2002) · Cellular and Molecular Life Sciences · doi:10.1007/s000180200009 · Cited by 75 · see citing works

Immune development in jejunal mucosa after colonization with selected commensal gut bacteria: A study in germ-free pigs

Haverson, K., Šinkorová, Z., Šinkora, J., Šver, L., & Bailey, M. (2007) · Veterinary Immunology and Immunopathology · doi:10.1016/j.vetimm.2007.05.022 · Cited by 73 · see citing works

Lactic acid bacterial colonization and human rotavirus infection influence distribution and frequencies of monocytes/macrophages and dendritic cells in neonatal gnotobiotic pigs

Zhang, W., Wen, K., Azevedo, M. S. P., et al. (2007) · Veterinary Immunology and Immunopathology · doi:10.1016/j.vetimm.2007.10.001 · Cited by 71 · see citing works

Systemic Control of Plasmacytoid Dendritic Cells by CD8+ T Cells and Commensal Microbiota

Fujiwara, D., Wei, B., Presley, L. L., Brewer, S., McPherson, M., Lewinski, M. A., Borneman, J., & Braun, J. G. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.180.9.5843 · Cited by 70 · see citing works

Inflammatory Tendencies and Overproduction of IL-17 in the Colon of Young NOD Mice Are Counteracted With Diet Change

Alam, C. M., Valkonen, S., Palagani, V., Jalava, J., Eerola, E., & Hänninen, A. L. M. (2010) · Diabetes · doi:10.2337/db10-0147 · Cited by 67 · see citing works

Commensal bacteria promote migration of mast cells into the intestine

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Breakdown of T cell tolerance and autoimmunity in primary immunodeficiency—lessons learned from monogenic disorders in mice and men

Westerberg, L. S., Klein, C., & Snapper, S. B. (2008) · Current Opinion in Immunology · doi:10.1016/j.coi.2008.10.004 · Cited by 64 · see citing works

Activation-Induced Cytidine Deaminase Deficiency Causes Organ-Specific Autoimmune Disease

Hase, K., Takahashi, D., Ebisawa, M., Kawano, S., Itoh, K., & Ohno, H. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003033 · Cited by 63 · see citing works

Microbial colonization induces oligoclonal expansions of intraepithelial CD8 T cells in the gut

Helgeland, L., Dissen, E., Dai, K., Midtvedt, T., Brandtzæg, P., & Vaage, J. T. (2004) · European Journal of Immunology · doi:10.1002/eji.200425122 · Cited by 62 · see citing works

Non-HLA associations with autoimmune diseases

Serrano, N. C., Millán, P. A., & Páez, M. C. (2005) · Autoimmunity Reviews · doi:10.1016/j.autrev.2005.06.009 · Cited by 56 · see citing works

Resident enteric microbiota and CD8+ T cells shape the abundance of marginal zone B cells

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Macrophages in the Small Intestinal Muscularis Externa of Embryos, Newborn and Adult Germ-Free Mice

Mikkelsen, H. B., Garbarsch, C., Tranum‐Jensen, J., & Thuneberg, L. (2004) · Journal of Molecular Histology · doi:10.1023/b:hijo.0000039840.86420.b7 · Cited by 54 · see citing works

Commensal gut bacteria and the etiopathogenesis of rheumatoid arthritis.

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Development and cytolytic function of intestinal intraepithelial T lymphocytes in antigen‐minimized mice

Kawaguchi-Miyashita, M., Shimizu, K., Nanno, M., SHIMADA, S., Watanabe, T., KOGA, Y., Matsuoka, Y., Ishikawa, H., HASHIMOTO, K., & Ohwaki, M. (1996) · Immunology · doi:10.1046/j.1365-2567.1996.d01-740.x · Cited by 51 · see citing works

SHORT PAPER

Ohkubo, T., TSUDA, M., TAMURA, M., et al. (1990) · Scandinavian Journal of Immunology · doi:10.1111/j.1365-3083.1990.tb03216.x · Cited by 51 · see citing works

Early arthritis and infection

Leirisalo‐Repo, M. (2005) · Current Opinion in Rheumatology · doi:10.1097/01.bor.0000166388.47604.8b · Cited by 46 · see citing works

Role of the Bowel Flora for Development of Immunity to hsp 65 and Arthritis in Three Experimental Models

Björk, J., Kleinau, S., Midtvedt, T., et al. (1994) · Scandinavian Journal of Immunology · doi:10.1111/j.1365-3083.1994.tb03518.x · Cited by 41 · see citing works

Phagocytosis, peritoneal influx, and enzyme activities in peritoneal macrophages from germfree, conventional, and ex-germfree mice

Mørland, B., & Midtvedt, T. (1984) · Infection and Immunity · doi:10.1128/iai.44.3.750-752.1984 · Cited by 39 · see citing works

Ontogeny of macrophage function to release superoxide anion in conventional and germfree mice

Mitsuyama, M., Ohara, R., Amako, K., Nomoto, K., Yokokura, T., & Nomoto, K. (1986) · Infection and Immunity · doi:10.1128/iai.52.1.236-239.1986 · Cited by 39 · see citing works

Peripheral Blood Neutrophils of Germ‐Free Rats Modified by In Vivo Granulocyte–Colony‐Stimulating Factor and Exposure to Natural Environment

Ohkubo, T., TSUDA, M., Suzuki, S., et al. (1999) · Scandinavian Journal of Immunology · doi:10.1046/j.1365-3083.1999.00456.x · Cited by 26 · see citing works

Origin and fate of IgE-bearing lymphocytes. II. Modulation of IgE isotype expression on Peyer's patch cells by feeding with certain bacteria and bacterial cell wall components or by thymectomy.

Durkin, H. G., Sm, C., Gaetjens, E., et al. (1989) · The Journal of Immunology · doi:10.4049/jimmunol.143.6.1777 · Cited by 23 · see citing works

Induction of intestinal lymphoid tissue formation by intrinsic and extrinsic signals

Finke, D. (2009) · Seminars in Immunopathology · doi:10.1007/s00281-009-0163-6 · Cited by 23 · see citing works

Immune mediators in the brain and peripheral tissues in autism spectrum disorder

Estes, M. L., & McAllister, A. K. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3978 · Cited by 514 · see citing works

Probiotics Regulate Gut Microbiota: An Effective Method to Improve Immunity

Wang, X., Zhang, P., & Zhang, X. (2021) · Molecules · doi:10.3390/molecules26196076 · Cited by 529 · see citing works

Differences in gut microbiota profile between women with active lifestyle and sedentary women

Bressa, C., Bailén-Andrino, M., Pérez-Santiago, J., González-Soltero, R., Pérez, M., Montalvo-Lominchar, M. G., Maté-Muñoz, J. L., Domínguez, R., Moreno, D., & Larrosa, M. (2017) · PLOS ONE · doi:10.1371/journal.pone.0171352 · Cited by 501 · see citing works

Weaning stress and gastrointestinal barrier development: implications for lifelong gut health in pigs

Moeser, A. J., Pohl, C. S., & Rajput, M. (2017) · Animal nutrition · doi:10.1016/j.aninu.2017.06.003 · Cited by 452 · see citing works

The role of the microbiome for human health: From basic science to clinical applications

Mohajeri, M. H., Brummer, R. J. M., Rastall, R. A., Weersma, R. K., Harmsen, H. J. M., Faas, M., & Eggersdorfer, M. (2018) · European Journal of Nutrition · doi:10.1007/s00394-018-1703-4 · Cited by 440 · see citing works

Immune System Dysregulation During Spaceflight: Potential Countermeasures for Deep Space Exploration Missions

Crucian, B. E., Choukèr, A., Simpson, R. J., Mehta, S., Marshall, G., Smith, S. M., Zwart, S. R., Heer, M., Ponomarev, S., Whitmire, A., et al. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01437 · Cited by 421 · see citing works

A Consideration of Biomarkers to be Used for Evaluation of Inflammation in Human Nutritional Studies

Calder, P. C., Ahluwalia, N., Albers, R., Bosco, N., Bourdet-Sicard, R., Haller, D., Holgate, S. T., Jönsson, L. S., Latulippe, M. E., Marcos, A., et al. (2013) · British Journal of Nutrition · doi:10.1017/s0007114512005119 · Cited by 425 · see citing works

Total fecal microbiota transplantation alleviates high-fat diet-induced steatohepatitis in mice via beneficial regulation of gut microbiota

Zhou, D., Pan, Q., Shen, F., Cao, H.-X., Ding, W.-J., Chen, Y.-W., & Fan, J.-G. (2017) · Scientific Reports · doi:10.1038/s41598-017-01751-y · Cited by 421 · see citing works

Intestinal flora and disease mutually shape the regional immune system in the intestinal tract

Zhou, B., Yuan, Y., Zhang, S., Guo, C., Li, X., Li, G., Xiong, W., & Zeng, Z. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00575 · Cited by 396 · see citing works

The athletic gut microbiota

Mohr, A. E., Jäger, R., Carpenter, K. C., Kerksick, C. M., Purpura, M., Townsend, J. R., West, N. P., Black, K., Gleeson, M., Pyne, D. B., et al. (2020) · Journal of the International Society of Sports Nutrition · doi:10.1186/s12970-020-00353-w · Cited by 378 · see citing works

Manipulating rumen microbiome and fermentation through interventions during early life: a review

Yáñez-Ruiz, D. R., Abecia, L., & Newbold, C. J. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.01133 · Cited by 336 · see citing works

Gut Microbiota, Immune System, and Bone

D’Amelio, P., & Sassi, F. (2018) · Calcified Tissue International · doi:10.1007/s00223-017-0331-y · Cited by 315 · see citing works

Host Genetics and Gut Microbiome: Challenges and Perspectives

Kurilshikov, A., Wijmenga, C., Fu, J., & Zhernakova, A. (2017) · Trends in Immunology · doi:10.1016/j.it.2017.06.003 · Cited by 309 · see citing works

Changes of colonic bacterial composition in Parkinson's disease and other neurodegenerative diseases

Gerhardt, S., & Mohajeri, M. H. (2018) · Nutrients · doi:10.3390/nu10060708 · Cited by 298 · see citing works

Gut Microbiota Drive Autoimmune Arthritis by Promoting Differentiation and Migration of Peyer’s Patch T Follicular Helper Cells

Teng, F., Klinger, C. N., Felix, K. M., Bradley, C. P., Wu, E., Tran, N. L., Umesaki, Y., & Wu, H.-J. J. (2016) · Immunity · doi:10.1016/j.immuni.2016.03.013 · Cited by 281 · see citing works

Importance of probiotics in the prevention and treatment of colorectal cancer

Eslami, M., Yousefi, B., Kokhaei, P., Hemati, M., Nejad, Z. R., Arabkari, V., & Namdar, A. (2019) · Journal of Cellular Physiology · doi:10.1002/jcp.28473 · Cited by 285 · see citing works

Interplay among gut microbiota, intestinal mucosal barrier and enteric neuro-immune system: a common path to neurodegenerative diseases?

Pellegrini, C., Antonioli, L., Colucci, R., Blandizzi, C., & Fornai, M. (2018) · Acta Neuropathologica · doi:10.1007/s00401-018-1856-5 · Cited by 270 · see citing works

Disturbance of the gut microbiota in early-life selectively affects visceral pain in adulthood without impacting cognitive or anxiety-related behaviors in male rats

O’Mahony, S. M., Felice, V. D., Nally, K., Savignac, H. M., Claesson, M. J., Scully, P., Woznicki, J., Hyland, N. P., Shanahan, F., Quigley, E. M., et al. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.07.054 · Cited by 272 · see citing works

A commensal symbiotic factor derived from <i>Bacteroides fragilis</i> promotes human CD39 ⁺ Foxp3 ⁺ T cells and T _reg function

Telesford, K. M., Yan, W., Ochoa-Reparaz, J., Pant, A., Kircher, C., Christy, M. A., Begum-Haque, S., Kasper, D. L., & Kasper, L. H. (2015) · Gut Microbes · doi:10.1080/19490976.2015.1056973 · Cited by 252 · see citing works

Cell surface polysaccharides of <i>Bifidobacterium bifidum</i> induce the generation of Foxp3 ⁺ regulatory T cells

Verma, R., Lee, C., Jeun, E.-J., Yi, J., Kim, K. S., Ghosh, A., Byun, S., Lee, C.-G., Kang, H.-J., Kim, G.-C., et al. (2018) · Science Immunology · doi:10.1126/sciimmunol.aat6975 · Cited by 242 · see citing works

Oral supplementation of healthy adults with 2′- <i>O</i> -fucosyllactose and lacto- <i>N</i> -neotetraose is well tolerated and shifts the intestinal microbiota

Elison, E., Vigsnaes, L. K., Rindom Krogsgaard, L., Rasmussen, J., Sørensen, N., McConnell, B., Hennet, T., Sommer, M. O. A., & Bytzer, P. (2016) · British Journal of Nutrition · doi:10.1017/s0007114516003354 · Cited by 218 · see citing works

Resetting microbiota by <i>Lactobacillus reuteri</i> inhibits T reg deficiency–induced autoimmunity via adenosine A2A receptors

He, B., Hoang, T. K., Wang, T., Ferris, M., Taylor, C. M., Tian, X., Luo, M., Tran, D. Q., Zhou, J., Tatevian, N., et al. (2017) · Journal of Experimental Medicine · doi:10.1084/jem.20160961 · Cited by 196 · see citing works

Gut Microbial Associations to Plasma Metabolites Linked to Cardiovascular Phenotypes and Risk: A Cross-Sectional Study

Kurilshikov, A., van den Munckhof, I. C. L., Chen, L., Bonder, M. J., Schraa, K., Rutten, J. H. W., Riksen, N. P., de Graaf, J., Oosting, M., Sanna, S., et al. (2019) · Circulation Research · doi:10.1161/circresaha.118.314642 · Cited by 178 · see citing works

Host genetic regulation of human gut microbial structural variation

Zhernakova, D. V., Wang, D., Liu, L., Andreu-Sánchez, S., Zhang, Y., Ruiz-Moreno, A. J., Peng, H., Plomp, N., Del Castillo-Izquierdo, Á., Gacesa, R., et al. (2024) · Nature · doi:10.1038/s41586-023-06893-w · Cited by 174 · see citing works

Intestinal Microbiota Influences Non-intestinal Related Autoimmune Diseases

Opazo, M. C., Ortega-Rocha, E. M., Coronado-Arrázola, I., Bonifaz, L. C., Boudin, H., Neunlist, M., Bueno, S. M., Kalergis, A. M., & Riedel, C. A. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.00432 · Cited by 179 · see citing works

Microbiota-gut-brain axis in health and disease: Is NLRP3 inflammasome at the crossroads of microbiota-gut-brain communications?

Pellegrini, C., Antonioli, L., Calderone, V., Colucci, R., Fornai, M., & Blandizzi, C. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101806 · Cited by 174 · see citing works

Gut microbiota modulates adoptive cell therapy via CD8α dendritic cells and IL-12

Uribe-Herranz, M., Bittinger, K., Rafail, S., Guedan, S., Pierini, S., Tanes, C., Ganetsky, A., Morgan, M. A., Gill, S., Tanyi, J. L., et al. (2018) · JCI Insight · doi:10.1172/jci.insight.94952 · Cited by 175 · see citing works

One health, fermented foods and gut microbiota

Bell, V., Ferrão, J., Pimentel, L., Pintado, M., & Fernandes, T. (2018) · Foods · doi:10.3390/foods7120195 · Cited by 188 · see citing works

Effects of the probiotic formulation SLAB51 in <i>in vitro</i> and <i>in vivo</i> Parkinson’s disease models

Castelli, V., d’Angelo, M., Lombardi, F., Alfonsetti, M., Antonosante, A., Catanesi, M., Benedetti, E., Palumbo, P., Cifone, M. G., Giordano, A., et al. (2020) · Aging · doi:10.18632/aging.102927 · Cited by 162 · see citing works

Gut microbiota composition correlates with changes in body fat content due to weight loss

Remely, M., Tesar, I., Hippe, B., Gnauer, S., Rust, P., & Haslberger, A. G. (2015) · Beneficial Microbes · doi:10.3920/bm2014.0104 · Cited by 162 · see citing works

Nonalcoholic Fatty Liver Disease Is Exacerbated in High-Fat Diet-Fed Gnotobiotic Mice by Colonization with the Gut Microbiota from Patients with Nonalcoholic Steatohepatitis

Chiu, C.-C., Ching, Y.-H., Li, Y.-P., Liu, J.-Y., Huang, Y.-T., Huang, Y.-W., Yang, S.-S., Huang, W.-C., & Chuang, H.-L. (2017) · Nutrients · doi:10.3390/nu9111220 · Cited by 160 · see citing works

Relevance of gutmicrobiota in cognition, behaviour and Alzheimer’s disease

de J.R. De-Paula, V., Forlenza, A. S., & Forlenza, O. V. (2018) · Pharmacological Research · doi:10.1016/j.phrs.2018.07.007 · Cited by 145 · see citing works

The effect of age on the intestinal mucus thickness, microbiota composition and immunity in relation to sex in mice

Elderman, M., Sovran, B., Hugenholtz, F., Graversen, K., Huijskes, M., Houtsma, E., Belzer, C., Boekschoten, M., de Vos, P., Dekker, J., et al. (2017) · PLOS ONE · doi:10.1371/journal.pone.0184274 · Cited by 145 · see citing works

Targeting gut microbiome: a novel and potential therapy for autism

Yang, Y., Tian, J., & Yang, B. (2018) · Life Sciences · doi:10.1016/j.lfs.2017.12.027 · Cited by 140 · see citing works

Host-Microbiota Interactions Shape Local and Systemic Inflammatory Diseases

Grigg, J. B., & Sonnenberg, G. F. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1601621 · Cited by 130 · see citing works

Unlocking the Potential of Probiotics: A Comprehensive Review on Research, Production, and Regulation of Probiotics

da Silva, T. F., Glória, R. D. A., Americo, M. F., Freitas, A. D. S., de Jesus, L. C. L., Barroso, F. A. L., Laguna, J. G., Coelho-Rocha, N. D., Tavares, L. M., le Loir, Y., et al. (2024) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-024-10247-x · Cited by 117 · see citing works

Can we ‘seize’ the gut microbiota to treat epilepsy?

De Caro, C., Iannone, L. F., Citraro, R., Striano, P., De Sarro, G., Constanti, A., Cryan, J. F., & Russo, E. (2019) · Neuroscience &amp; Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.10.002 · Cited by 110 · see citing works

The microbiota–microglia axis in central nervous system disorders

Mossad, O., & Erny, D. (2020) · Brain Pathology · doi:10.1111/bpa.12908 · Cited by 98 · see citing works

The Influence of Ketogenic Diet on Gut Microbiota: Potential Benefits, Risks and Indications

Santangelo, A., Corsello, A., Spolidoro, G. C. I., Trovato, C. M., Agostoni, C., Orsini, A., Milani, G. P., & Peroni, D. G. (2023) · Nutrients · doi:10.3390/nu15173680 · Cited by 80 · see citing works

Geographic Differences in Gut Microbiota Composition Impact Susceptibility to Enteric Infection

Porras, A. M., Shi, Q., Zhou, H., Callahan, R., Montenegro-Bethancourt, G., Solomons, N., & Brito, I. L. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109457 · Cited by 74 · see citing works

A dynamic atlas of immunocyte migration from the gut

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<i>Escherichia coli</i> infection induces autoimmune cholangitis and anti-mitochondrial antibodies in non-obese diabetic (NOD).B6 ( <i>Idd10/Idd18</i> ) mice

Wang, J. J., Yang, G.-X., Zhang, W. C., Lu, L., Tsuneyama, K., Kronenberg, M., Véla, J. L., Lopez-Hoyos, M., He, X.-S., Ridgway, W. M., et al. (2014) · Clinical and Experimental Immunology · doi:10.1111/cei.12224 · Cited by 74 · see citing works

How the gut microbiome regulates host immune responses to viral vaccines

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Experimentally induced metamorphosis in highly regenerative axolotl (ambystoma mexicanum) under constant diet restructures microbiota

Demircan, T., Ovezmyradov, G., Yıldırım, B., Keskin, İ., İlhan, A. E., Fesçioğlu, E. C., Öztürk, G., & Yıldırım, S. (2018) · Scientific Reports · doi:10.1038/s41598-018-29373-y · Cited by 45 · see citing works

The Gut Microbiota’s Role in Neurological, Psychiatric, and Neurodevelopmental Disorders

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Gut Microbiota–Related Biomarkers in Immuno-Oncology

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