Host-Microbiota Interactions Shape Local and Systemic Inflammatory Diseases

Structure, function and diversity of the healthy human microbiome

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Diet rapidly and reproducibly alters the human gut microbiome

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Linking long-term dietary patterns with gut microbial enterotypes

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Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

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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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Commensal microbe-derived butyrate induces the differentiation of colonic regulatory T cells

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The Microbial Metabolites, Short-Chain Fatty Acids, Regulate Colonic T _reg Cell Homeostasis

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A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

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The gut microbiota shapes intestinal immune responses during health and disease

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Metabolites produced by commensal bacteria promote peripheral regulatory T-cell generation

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

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

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Genetics and pathogenesis of inflammatory bowel disease

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The gut microbiota and host health: a new clinical frontier

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

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Role of the gut microbiota in immunity and inflammatory disease

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Are We Really Vastly Outnumbered? Revisiting the Ratio of Bacterial to Host Cells in Humans

Sender, R., Fuchs, S., & Milo, R. (2016) · Cell · doi:10.1016/j.cell.2016.01.013 · Cited by 2,050 · see citing works

How colonization by microbiota in early life shapes the immune system

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NLRP6 Inflammasome Regulates Colonic Microbial Ecology and Risk for Colitis

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Interleukin-22 mediates early host defense against attaching and effacing bacterial pathogens

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Intestinal homeostasis and its breakdown in inflammatory bowel disease

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The anti-inflammatory and immunosuppressive effects of glucocorticoids, recent developments and mechanistic insights

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Specific Microbiota Direct the Differentiation of IL-17-Producing T-Helper Cells in the Mucosa of the Small Intestine

Ivanov, I. I., Frutos, R. D. L., Manel, N., Yoshinaga, K., Rifkin, D. B., Sartor, R. B., Finlay, B. B., & Littman, D. R. (2008) · Cell Host &amp; Microbe · doi:10.1016/j.chom.2008.09.009 · Cited by 1,770 · see citing works

Epidemiology and risk factors for IBD

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Microbial Exposure During Early Life Has Persistent Effects on Natural Killer T Cell Function

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

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Reciprocal interactions of the intestinal microbiota and immune system

Maynard, C. L., Elson, C. O., Hatton, R. D., & Weaver, C. T. (2012) · Nature · doi:10.1038/nature11551 · Cited by 1,598 · cited 1× · see citing works

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

Wu, H.-J., Ivanov, I. I., Darce, J., Hattori, K., Shima, T., Umesaki, Y., Littman, D. R., Benoist, C., & Mathis, D. (2010) · Immunity · doi:10.1016/j.immuni.2010.06.001 · Cited by 1,577 · see citing works

Fecal Microbiota Transplantation Induces Remission in Patients With Active Ulcerative Colitis in a Randomized Controlled Trial

Moayyedi, P., Surette, M. G., Kim, P. T., Libertucci, J., Wolfe, M., Onischi, C., Armstrong, D., Marshall, J. K., Kassam, Z., Reinisch, W., et al. (2015) · Gastroenterology · doi:10.1053/j.gastro.2015.04.001 · Cited by 1,499 · see citing works

CARD9 impacts colitis by altering gut microbiota metabolism of tryptophan into aryl hydrocarbon receptor ligands

Lamas, B., Richard, M. L., Leducq, V., Pham, H.-P., Michel, M.-L., Da Costa, G., Bridonneau, C., Jegou, S., Hoffmann, T. W., Natividad, J. M., et al. (2016) · Nature Medicine · doi:10.1038/nm.4102 · Cited by 1,482 · see citing works

Inflammatory Bowel Disease and Mutations Affecting the Interleukin-10 Receptor

Glocker, E., Kotlarz, D., Boztuǧ, K., Gertz, E. M., Schäffer, A. A., Noyan, F., Perro, M., Diestelhorst, J., Saborowski, A. L., Murugan, D., et al. (2009) · New England Journal of Medicine · doi:10.1056/nejmoa0907206 · Cited by 1,452 · see citing works

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

Gaboriau-Routhiau, V., Rakotobe, S., Lécuyer, E., Mulder, I., Lan, A., Bridonneau, C., Rochet, V., Pisi, A., De Paepe, M., Brandi, G., et al. (2009) · Immunity · doi:10.1016/j.immuni.2009.08.020 · Cited by 1,452 · see citing works

The role of gut microbiota in immune homeostasis and autoimmunity

Wu, H.-J., & Wu, E. (2012) · Gut Microbes · doi:10.4161/gmic.19320 · Cited by 1,426 · see citing works

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

Lee, Y. K., Menezes, J. S., Umesaki, Y., & Mazmanian, S. K. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1000082107 · Cited by 1,323 · see citing works

Host-Mediated Inflammation Disrupts the Intestinal Microbiota and Promotes the Overgrowth of Enterobacteriaceae

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Immunoglobulin A Coating Identifies Colitogenic Bacteria in Inflammatory Bowel Disease

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Secretory IgA's complex roles in immunity and mucosal homeostasis in the gut

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Paneth cells, antimicrobial peptides and maintenance of intestinal homeostasis

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Th17 cell induction by adhesion of microbes to intestinal epithelial cells

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Are innate immune signaling pathways in plants and animals conserved?

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Host-Derived Nitrate Boosts Growth of <i>E. coli</i> in the Inflamed Gut

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Innate lymphoid cells as regulators of immunity, inflammation and tissue homeostasis

Klose, C. S. N., & Artis, D. (2016) · Nature Immunology · doi:10.1038/ni.3489 · Cited by 954 · see citing works

Molecular mimicry and autoimmune disease

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Findings From a Randomized Controlled Trial of Fecal Transplantation for Patients With Ulcerative Colitis

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Extraintestinal Manifestations of Inflammatory Bowel Disease

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

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Individual intestinal symbionts induce a distinct population of RORγ ⁺ regulatory T cells

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The microbiota regulates type 2 immunity through RORγt ⁺ T cells

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

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Innate lymphoid cells regulate CD4+ T-cell responses to intestinal commensal bacteria

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Innate Lymphoid Cells Promote Anatomical Containment of Lymphoid-Resident Commensal Bacteria

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A gut-vascular barrier controls the systemic dissemination of bacteria

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Fecal microbiota transplantation and emerging applications

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

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IL-1β mediates chronic intestinal inflammation by promoting the accumulation of IL-17A secreting innate lymphoid cells and CD4+ Th17 cells

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Intestinal Bacteria and the Regulation of Immune Cell Homeostasis

Hill, D. A., & Artis, D. (2010) · Annual Review of Immunology · doi:10.1146/annurev-immunol-030409-101330 · Cited by 586 · see citing works

CD4+ Lymphoid Tissue-Inducer Cells Promote Innate Immunity in the Gut

Sonnenberg, G. F., Monticelli, L. A., Elloso, M. M., Fouser, L. A., & Artis, D. (2010) · Immunity · doi:10.1016/j.immuni.2010.12.009 · Cited by 573 · see citing works

NOD2-mediated dysbiosis predisposes mice to transmissible colitis and colorectal cancer

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Innate lymphoid cells regulate intestinal epithelial cell glycosylation

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Innate and Adaptive Humoral Responses Coat Distinct Commensal Bacteria with Immunoglobulin A

Bunker, J. J., Flynn, T. M., Koval, J., Shaw, D. G., Meisel, M., McDonald, B. D., Ishizuka, I. E., Dent, A. L., Wilson, P. C., Jabrì, B., et al. (2015) · Immunity · doi:10.1016/j.immuni.2015.08.007 · Cited by 557 · see citing works

Development and maintenance of intestinal regulatory T cells

Tanoue, T., Atarashi, K., & Honda, K. (2016) · Nature Reviews Immunology · doi:10.1038/nri.2016.36 · Cited by 553 · see citing works

An IL-23R/IL-22 Circuit Regulates Epithelial Serum Amyloid A to Promote Local Effector Th17 Responses

Sano, T., Huang, W., Hall, J. A., Yang, Y., Chen, A., Gavzy, S. J., Lee, J.-Y., Ziel, J. W., Miraldi, E. R., Domingos, A. I., et al. (2015) · Cell · doi:10.1016/j.cell.2015.08.061 · Cited by 547 · see citing works

Dietary antigens limit mucosal immunity by inducing regulatory T cells in the small intestine

Kim, K. S., Hong, S., Han, D., Yi, J., Jung, J., Yang, B., Lee, J. Y., Lee, M., & Surh, C. D. (2016) · Science · doi:10.1126/science.aac5560 · Cited by 541 · see citing works

Rapid fucosylation of intestinal epithelium sustains host–commensal symbiosis in sickness

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Group 3 innate lymphoid cells mediate intestinal selection of commensal bacteria–specific CD4 + T cells

Hepworth, M. R., Fung, T. C., Masur, S. H., Kelsen, J. R., McConnell, F. M., Dubrot, J., Withers, D. R., Hugues, S., Farrar, M. A., Reith, W., et al. (2015) · Science · doi:10.1126/science.aaa4812 · Cited by 515 · see citing works

Increased Proportions of Bifidobacterium and the Lactobacillus Group and Loss of Butyrate-Producing Bacteria in Inflammatory Bowel Disease

Wang, W., Chen, L., Zhou, R., Wang, X., Song, L., Huang, S., Wang, G., & Xia, B. (2014) · Journal of Clinical Microbiology · doi:10.1128/jcm.01500-13 · Cited by 509 · see citing works

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

Ochoa-Repáraz, J., Mielcarz, D. W., Wang, Y., Begum-Haque, S., Dasgupta, S., Kasper, D. L., & Kasper, L. H. (2010) · Mucosal Immunology · doi:10.1038/mi.2010.29 · Cited by 507 · see citing works

Innate lymphoid cells in the initiation, regulation and resolution of inflammation

Sonnenberg, G. F., & Artis, D. (2015) · Nature Medicine · doi:10.1038/nm.3892 · Cited by 503 · see citing works

Role of mucus layers in gut infection and inflammation

Hansson, G. C. (2011) · Current Opinion in Microbiology · doi:10.1016/j.mib.2011.11.002 · Cited by 473 · see citing works

Microbiota restricts trafficking of bacteria to mesenteric lymph nodes by CX3CR1hi cells

Diehl, G. E., Longman, R., Zhang, J.-X., Bréart, B., Galan, C., Cuesta, A., Schwab, S. R., & Littman, D. R. (2013) · Nature · doi:10.1038/nature11809 · Cited by 472 · see citing works

Gut Microbiota-Induced Immunoglobulin G Controls Systemic Infection by Symbiotic Bacteria and Pathogens

Zeng, M. Y., Cisalpino, D., Varadarajan, S., Hellman, J., Warren, H. S., Cascalho, M., Inohara, N., & Núñez, G. (2016) · Immunity · doi:10.1016/j.immuni.2016.02.006 · Cited by 417 · see citing works

The role of the immune system in governing host-microbe interactions in the intestine

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Microbiota-Dependent Activation of an Autoreactive T Cell Receptor Provokes Autoimmunity in an Immunologically Privileged Site

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Characterization of Innate Lymphoid Cells in Human Skin and Blood Demonstrates Increase of NKp44+ ILC3 in Psoriasis

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Diet in the Pathogenesis and Treatment of Inflammatory Bowel Diseases

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Functional characterization of IgA-targeted bacterial taxa from undernourished Malawian children that produce diet-dependent enteropathy

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Identifying gut microbe-host phenotype relationships using combinatorial communities in gnotobiotic mice

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Antimicrobial Defense of the Intestine

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Maternal IgG and IgA Antibodies Dampen Mucosal T Helper Cell Responses in Early Life

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Systematic review: faecal microbiota transplantation in the management of inflammatory bowel disease

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Autoinducer-2 May Be a New Biomarker for Monitoring Neonatal Necrotizing Enterocolitis

Fu, C.-Y., Li, L.-Q., Yang, T., She, X., Ai, Q., & Wang, Z.-L. (2020) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.00140 · Cited by 34 · see citing works

Gut immune microenvironment and autoimmunity

Wang, Q., Lu, Q., Jia, S., & Zhao, M. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.110842 · Cited by 33 · see citing works

Influence of a High-Impact Multidimensional Rehabilitation Program on the Gut Microbiota of Patients with Multiple Sclerosis

Barone, M., Mendozzi, L., D’Amico, F., Saresella, M., Rampelli, S., Piancone, F., Rosa, F. L., Marventano, I., Clerici, M., d’Arma, A., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22137173 · Cited by 31 · see citing works

Gut Microbiota Dysbiosis in COVID-19: Modulation and Approaches for Prevention and Therapy

Giménez, V. M. M., Modrego, J., Gómez‐Garré, D., Manucha, W. A., & Heras, N. D. L. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241512249 · Cited by 31 · see citing works

Can the FUT2 Non-secretor Phenotype Associated With Gut Microbiota Increase the Children Susceptibility for Type 1 Diabetes? A Mini Review

Giampaoli, O., Conta, G., Calvani, R., & Miccheli, A. (2020) · Frontiers in Nutrition · doi:10.3389/fnut.2020.606171 · Cited by 30 · see citing works

Inflammation and Arterial Stiffness as Drivers of Cardiovascular Risk in Kidney Disease

Cicero, L. L., Lentini, P. L. M., Sessa, C., Castellino, N., D’anca, A., Torrisi, I., Marcantoni, C., Castellino, P., Santoro, D., & Zanoli, L. (2024) · Cardiorenal Medicine · doi:10.1159/000542965 · Cited by 29 · see citing works

Intestinal protozoan infections shape fecal bacterial microbiota in children from Guinea-Bissau

von Huth, S., Thingholm, L. B., Kofoed, P., Bang, C., Rühlemann, M. C., Franke, A., & Holmskov, U. (2021) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0009232 · Cited by 28 · see citing works

The oral microbiome of patients undergoing treatment for severe aplastic anemia: a pilot study

Ames, N. J., Barb, J. J., Ranucci, A., Kim, H., Mudra, S. E., Cashion, A. K., Townsley, D. M., Childs, R. W., Paster, B. J., Faller, L. L., et al. (2019) · Annals of Hematology · doi:10.1007/s00277-019-03599-w · Cited by 29 · see citing works

Effects of antibiotics and metals on lung and intestinal microbiome dysbiosis after sub-chronic lower-level exposure of air pollution in ageing rats

Laiman, V., Lo, Y., Chen, H., Yuan, T., Hsiao, T.-C., Chen, J., Chang, C.-W., Lin, T.-C., Li, S., Chen, Y.-Y., et al. (2022) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2022.114164 · Cited by 27 · see citing works

Epithelial-neuronal-immune cell interactions: Implications for immunity, inflammation, and tissue homeostasis at mucosal sites

Emanuel, E., Arifuzzaman, M., & Artis, D. (2024) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2024.02.004 · Cited by 24 · see citing works

Psychosocial and neurobiological aspects of the worldwide refugee crisis: From vulnerability to resilience

Anisman, H., Doubad, D., Asokumar, A., & Matheson, K. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105859 · Cited by 25 · see citing works

Targeted modulation of gut and intra-tumor microbiota to improve the quality of immune checkpoint inhibitor responses

Wang, W., Fan, J., Zhang, C., Huang, Y., Chen, Y., Fu, S., & Wu, J. (2024) · Microbiological Research · doi:10.1016/j.micres.2024.127668 · Cited by 23 · see citing works

Anti-microbial Antibodies, Host Immunity, and Autoimmune Disease

Zhang, P., Minardi, L. M., Kuenstner, J. T., Zekan, S. M., & Kruzelock, R. (2018) · Frontiers in Medicine · doi:10.3389/fmed.2018.00153 · Cited by 22 · see citing works

The role of complex interactions between the intestinal flora and host in regulating intestinal homeostasis and inflammatory bowel disease

Li, S., Xu, K., Cheng, Y., Chen, L., Yi, A., Xiao, Z., Zhao, X., Chen, M., Tian, Y., Wei, M., et al. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1188455 · Cited by 21 · see citing works

The distribution characteristics of intestinal microbiota in children with community-acquired pneumonia under five Years of age

Ren, X., Gamallat, Y., Liu, D., Zhu, Y., Meyiah, A., Yan, C., Shang, D., & Xin, Y. (2020) · Microbial Pathogenesis · doi:10.1016/j.micpath.2020.104062 · Cited by 20 · see citing works

Shifts in microbial diversity, composition, and functionality in the gut and genital microbiome during a natural SIV infection in vervet monkeys

Jasinska, A. J., Dong, T. S., Lagishetty, V., Katzka, W. R., Jacobs, J. P., Schmitt, C. A., Cramer, J. D., Ma, D., Coetzer, W. G., Grobler, J. P., et al. (2020) · Microbiome · doi:10.1186/s40168-020-00928-4 · Cited by 20 · see citing works

Failure of the Anti-Inflammatory Parasitic Worm Product ES-62 to Provide Protection in Mouse Models of Type I Diabetes, Multiple Sclerosis, and Inflammatory Bowel Disease

Doonan, J., Thomas, D., Wong, M. H., Ramage, H. J., Al‐Riyami, L., Lumb, F. E., Bell, K. S., Fairlie‐Clarke, K. J., Suckling, C. J., Michelsen, K. S., et al. (2018) · Molecules · doi:10.3390/molecules23102669 · Cited by 20 · see citing works

The gut microbiota and its metabolites: novel therapeutic targets for inflammatory bowel disease

Shen, X. Z., Li, Y., Wang, D., & Sun, K. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1690279 · Cited by 24 · see citing works

Immune Homeostasis: New Role of Micro- and Macroelements, Healthy Microbiota

Bulgakova, S. V., & Romanchuk, N. (2020) · Bulletin of Science and Practice · doi:10.33619/2414-2948/59/22 · Cited by 17 · see citing works

Insulin resistance corresponds with a progressive increase in NOD1 in high fat diet-fed mice

Sharma, A., Singh, S., Mishra, A., Rai, A., Ahmad, I., Ahmad, S., Gulzar, F., Schertzer, J., Shrivastava, A., & Tamrakar, A. (2022) · Endocrine · doi:10.1007/s12020-022-02995-z · Cited by 15 · see citing works

Lactoferrin Alleviates Lipopolysaccharide-Induced Infantile Intestinal Immune Barrier Damage by Regulating an ELAVL1-Related Signaling Pathway

Li, C., Liu, X., Huang, Z., Zhai, Y., Li, H., & Wu, J. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232213719 · Cited by 17 · see citing works

Dietary supplementation of laminarin improves the reproductive performance of sows and the growth of suckling piglets

Zhang, P., Jiang, G., Ma, C., Wang, Y., Yan, E., He, L., Guo, J., Zhang, X., & Yin, J. (2023) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-023-00920-6 · Cited by 17 · see citing works

Microbiota metabolites affect sleep as drivers of brain‑gut communication (Review)

Cheng, H. Y., Yang, W., Xu, H., Zhu, W., Gong, A., Yang, X., Li, S., & Xu, H. (2025) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2025.5571 · Cited by 16 · see citing works

The resistome and microbiome of wastewater treatment plant workers – The AWARE study

Berglund, F., Rodríguez-Molina, D., Pîrcălăbioru, G. G., Blaak, H., Chifiriuc, M. C., Barbu, I. C., Flach, C., Gheorghe-Barbu, I., Marutescu, L. G., Popa, M., et al. (2023) · Environment International · doi:10.1016/j.envint.2023.108242 · Cited by 14 · see citing works

The interactions along the microbiota—gut—brain axis in the regulation of circadian rhythms, sleep mechanisms and disorders

Shirolapov, I. V., Витальевна, Г. О., Kovalev, A. M., Shafigullina, L. R., Ulivanova, V. A., Kozlov, A. V., Еreshchenko, A. A., Lyamin, A. V., & Zakharov, A. V. (2024) · S S Korsakov Journal of Neurology and Psychiatry · doi:10.17116/jnevro202412405279 · Cited by 13 · see citing works

The Immune System: Our Body’s Homeland Security Against Disease

Vojdani, A., Vojdani, E., & Vojdani, C. (2020) · Springer eBooks · doi:10.1007/978-3-030-30730-1_19 · Cited by 12 · see citing works

Colonization by Akkermansia muciniphila modulates central nervous system autoimmunity in an ecological context-dependent manner

Peipert, D., Montgomery, T. L., Toppen, L. C., Lee, M. F. J., Scarborough, M., & Krementsov, D. N. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1655428 · Cited by 11 · see citing works

Potential roles of the interactions between gut microbiota and metabolites in LPS-induced intrauterine inflammation (IUI) and associated preterm birth (PTB)

Jia, B., Tang, L., Liu, H., Chen, W., Chen, Q., Zhong, M., & Yin, A. (2024) · Journal of Translational Medicine · doi:10.1186/s12967-023-04603-8 · Cited by 11 · see citing works

Fucose Ameliorates Tritrichomonas sp.-Associated Illness in Antibiotic-Treated Muc2−/− Mice

Achasova, K. M., Kozhevnikova, E. N., Borisova, M. A., & Litvinova, E. A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221910699 · Cited by 11 · see citing works

Imbalance of the Gut Microbiota May Be Associated with Missed Abortions: A Perspective Study from a General Hospital of Hunan Province

Gao, B., Zhao, X., Liu, X., Yang, X., Zhang, A., Huang, H., Liou, Y., & Xu, D. (2021) · Journal of Immunology Research · doi:10.1155/2021/5571894 · Cited by 10 · see citing works

Impact of oral microbiota on pathophysiology of GVHD

Yamamoto, A., Kambara, Y., & Fujiwara, H. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1132983 · Cited by 10 · see citing works

Intestinal microbiota and health

Kalip, K., & Atak, N. (2018) · Türkiye Halk Sağlığı Dergisi · doi:10.20518/tjph.458203 · Cited by 10 · see citing works

Commensal Microbes Affect Host Humoral Immunity to Bordetella pertussis Infection

Zhang, Y., Ran, Z., Tian, M., Zhou, Y., Yang, J., Yin, J. J., Lu, D., Li, R. Q., & Zhong, J. S. (2019) · Infection and Immunity · doi:10.1128/iai.00421-19 · Cited by 10 · see citing works

An in vitro intestinal model captures immunomodulatory properties of the microbiota in inflammation

Lock, J. Y., Caboni, M., Strandwitz, P., Morrissette, M., DiBona, K. C., Joughin, B. A., Lewis, K., & Carrier, R. L. (2022) · Gut Microbes · doi:10.1080/19490976.2022.2039002 · Cited by 9 · see citing works

Vascular endothelial growth factor encoded by Parapoxviruses can regulate metabolism and survival of triple negative breast cancer cells

Bose, D., Banerjee, S., Singh, R. K., Wise, L. M., & Robertson, E. S. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-03203-4 · Cited by 9 · see citing works

The impact of perinatal maternal stress on the maternal and infant gut and human milk microbiomes: A scoping review

Ryan, N., O’Mahony, S. M., Leahy‐Warren, P., Philpott, L. F., & Mulcahy, H. (2025) · PLoS ONE · doi:10.1371/journal.pone.0318237 · Cited by 8 · see citing works

Hemostasis and Cognitive Brain: 5P-Medicine and Chronotherapy of Arterial Hypertension

Pyatin, V. F., Maslova, O., Romanchuk, N., Bulgakova, S. V., & Volobuev, A. N. (2021) · Bulletin of Science and Practice · doi:10.33619/2414-2948/66/16 · Cited by 8 · see citing works

Developmental immunology and role of host defenses in fetal and neonatal susceptibility to infection

Lewis, D. B., Weitkamp, J.-H., & Levy, O. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-79525-8.00013-5 · Cited by 7 · see citing works

Soil intake modifies the gut microbiota and alleviates Th2-type immune response in an ovalbumin-induced asthma mouse model

Li, M., Li, N., Dong, Y., Zhang, H., Bai, Z., Zhang, R., Fei, Z., Zhu, W., Xiao, P., Sun, X. S., et al. (2024) · World Allergy Organization Journal · doi:10.1016/j.waojou.2024.100897 · Cited by 8 · see citing works

Cross—reactivity of antibodies against microbial proteins to human tissues as basis of Crohn’s disease and other autoimmune diseasesPreprint

Zhang, P., Minardi, L. M., Kuenstner, J. T., Zekan, S. M., Zhu, F., Hu, Y., & Kruzelock, R. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/116574 · Cited by 8 · see citing works

Correlation Between the Gut Microbiome and Immunotherapy Response in Inflammatory Bowel Disease: A Systematic Review of the Literature

Karpinska-Leydier, K., Amirthalingam, J., Alshowaikh, K., Jayarathna, A. I., Salibindla, D. B. A. M. R., Paidi, G., & Ergin, H. E. (2021) · Cureus · doi:10.7759/cureus.16808 · Cited by 6 · see citing works

Fatty is not that bad: feeding short-chain fatty acids to restrain autoimmunity

Brevi, A., & Bellone, M. (2017) · Cellular and Molecular Immunology · doi:10.1038/cmi.2017.52 · Cited by 7 · see citing works

Maternal vaccination against group B Streptococcus glyceraldehyde-3-phosphate dehydrogenase leads to gut dysbiosis in the offspring

Andrade, E. B., Lorga, I., Roque, S., Geraldo, R., Mesquita, P., Castro, R., Costa, A. L., Costa, M. M., Faustino, A., Ribeiro, A., et al. (2022) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2022.04.004 · Cited by 7 · see citing works

Intestinal microbiota and nutrients as determinants of nervous system function. Part I. Gastrointestinal microbiota

Skonieczna‐Żydecka, K., Łoniewski, I., Maciejewska, D., & Marlicz, W. M. (2017) · Aktualności Neurologiczne · doi:10.15557/an.2017.0020 · Cited by 7 · see citing works

The Role of Interactions along the Brain–Gut–Microbiome Axis in the Regulation of Circadian Rhythms, Sleep Mechanisms, and Their Disorders

Shirolapov, I. V., Витальевна, Г. О., Kovalev, A. M., Shafigullina, L. R., Ulivanova, V. A., Kozlov, A. V., Еreshchenko, A. A., Lyamin, A. V., & Zakharov, A. V. (2024) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-024-01712-9 · Cited by 6 · see citing works

Antibody Profiling of Microbial Antigens in the Blood of COVID-19 mRNA Vaccine Recipients Using Microbial Protein Microarrays

Saito, H., Yoshimura, H., Yoshida, M., Tani, Y., Kawashima, M., Uchiyama, T., Zhao, T., Yamamoto, C., Kobashi, Y., Sawano, T., et al. (2023) · Vaccines · doi:10.3390/vaccines11111694 · Cited by 6 · see citing works

Plasmon-activated water as a therapeutic strategy in Alzheimer’s disease by altering gut microbiota

Cheng, C., Liu, Y., Yang, Y. S. H., Lin, K., Wu, D., Liu, Y., Chang, C., Hong, C., & Hu, C. (2023) · Aging · doi:10.18632/aging.204706 · Cited by 6 · see citing works

The Synbiotic Role of Mushrooms: is Germanium a Bioactive Prebiotic Player? A Review Article

Ferrão, J., Bell, Chaquisse, E., Garrine, C. M. L. P., & Fernandes, T. H. (2019) · doi:10.12691/ajfn-7-1-5 · Cited by 7 · see citing works

Molecular Diversity of Gut Microbiota and Short Chain Fatty Acids in Egyptian Adults Following Dietary Intervention with Fermented Sobya

Labib, E., Blaut, M., Hussein, L., Goud, M., Kramer, D. L., Paliy, O., Ganesh, B. P., Schümann, P., Pukall, R. ⁄. D., Woting, A., et al. (2018) · doi:10.4172/2476-2059.1000139 · Cited by 5 · see citing works

Antibiotic drug use in the five years preceding the diagnosis of multiple sclerosis

Darvishi, S., Donnachie, E., Uibel, P., Flaskamp, M., Gasperi, C., Hapfelmeier, A., & Hemmer, B. (2025) · Multiple Sclerosis and Related Disorders · doi:10.1016/j.msard.2025.106366 · Cited by 4 · see citing works

Impact of exclusive enteral nutrition on the gut microbiome of children with medical complexity

Beauchamp‐Walters, J., Aleti, G., Herrera, L., Debelius, J. W., Lima, N., Dalal, P. B., Hong, S., Knight, R. D., & Rhee, K. E. (2022) · Journal of Parenteral and Enteral Nutrition · doi:10.1002/jpen.2392 · Cited by 4 · see citing works

Bidirectional association between infectious gastroenteritis and inflammatory bowel disease: a population-based study

Tu, K.-C., Yu, R.-Y., Lin, Y., Chien, C.-C., & Lu, C. (2023) · European journal of medical research · doi:10.1186/s40001-023-01324-y · Cited by 4 · see citing works

Dual burden of infectious and chronic disease in low-resource U.S. communities: examining relationships between infection, adiposity, and inflammation

Gildner, T. E., Urlacher, S. S., Nemeth, K. L., Beauregard, J. A., Nash, M. P., Zhang, A., Waimon, S., & Cepon‐Robins, T. J. (2024) · Annals of Human Biology · doi:10.1080/03014460.2024.2368851 · Cited by 4 · see citing works

Role of monolaurin additive with medium-chain fatty acids against dextran sulfate sodium-induced acute colitis through down regulating the oxidative stress in wistar rats

Ali, S. (2023) · The Pakistan Journal of Agricultural Sciences · doi:10.21162/pakjas/23.30 · Cited by 4 · see citing works

A short-term bioreactor assay to assess the effect of essential oils on a microbiota derived from piglet’s intestinal content

Bellerose, M., Fravalo, P., Mainville, I., Arcand, Y., & Thibodeau, A. (2023) · Acta veterinaria Scandinavica · doi:10.1186/s13028-023-00679-w · Cited by 3 · see citing works

The immune system and the gut microbiota: friends or foes?

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Regulation of Host Immunity by the Gut Microbiota

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Host-microbe interactions at barrier tissues and immunomodulation: a scoping review

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Interplay between gut microbiota in immune homeostasis and inflammatory diseases

Tiwari, N., Suri, M., Upadhyay, J., Ansari, M. N., & Samad, A. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-99988-5.00016-4 · Cited by 1 · see citing works

Interaction between microbiota and immunity in health and disease

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