Diet-Derived Short Chain Fatty Acids Stimulate Intestinal Epithelial Cells To Induce Mucosal Tolerogenic Dendritic Cells

Introducing mothur: Open-Source, Platform-Independent, Community-Supported Software for Describing and Comparing Microbial Communities

Schloss, P. D., Westcott, S. L., Ryabin, T., Hall, J. R., Hartmann, M., Hollister, E. B., Lesniewski, R. A., Oakley, B. B., Parks, D. H., Robinson, C. J., et al. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.01541-09 · Cited by 19,549

Ultra-high-throughput microbial community analysis on the Illumina HiSeq and MiSeq platforms

Caporaso, J. G., Lauber, C. L., Walters, W. A., Berg-Lyons, D., Huntley, J., Fierer, N., Owens, S. M., Betley, J., Fraser, L., Bauer, M., et al. (2012) · The ISME Journal · doi:10.1038/ismej.2012.8 · Cited by 8,839

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

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

Furusawa, Y., Obata, Y., Fukuda, S., Endo, T. A., Nakato, G., Takahashi, D., Nakanishi, Y., Uetake, C., Kato, K., Kato, T., et al. (2013) · Nature · doi:10.1038/nature12721 · Cited by 5,549

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

Arpaia, N., Campbell, C., Fan, X., Dikiy, S., van der Veeken, J., deRoos, P., Liu, H., Cross, J. R., Pfeffer, K., Coffer, P. J., et al. (2013) · Nature · doi:10.1038/nature12726 · Cited by 4,838

Treg induction by a rationally selected mixture of Clostridia strains from the human microbiota

Atarashi, K., Tanoue, T., Oshima, K., Suda, W., Nagano, Y., Nishikawa, H., Fukuda, S., Saito, T., Narushima, S., Hase, K., et al. (2013) · Nature · doi:10.1038/nature12331 · Cited by 2,872

Gut Microbiota Metabolism of Dietary Fiber Influences Allergic Airway Disease and Hematopoiesis

Trompette, A., Gollwitzer, E. S., Yadava, K., Sichelstiel, A. K., Sprenger, N., Ngom-Bru, C., Blanchard, C., Junt, T., Nicod, L. P., Harris, N. L., et al. (2014) · Nature Medicine · doi:10.1038/nm.3444 · Cited by 2,862

A functionally specialized population of mucosal CD103+ DCs induces Foxp3+ regulatory T cells via a TGF-β– and retinoic acid–dependent mechanism

Coombes, J. L., Siddiqui, K. R. R., Arancibia-Cárcamo, C. V., Hall, J. A., Sun, C., Belkaid, Y., & Powrie, F. M. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20070590 · Cited by 2,708

Butyrate enhances the intestinal barrier by facilitating tight junction assembly via activation of AMP-activated protein kinase in Caco-2 cell monolayers

Peng, L., Li, Z.-R., Green, R. S., Holzmanr, I. R., & Lin, J. (2009) · The Journal of Nutrition · doi:10.3945/jn.109.104638 · Cited by 2,130

Regulation of short-chain fatty acid production

Macfarlane, S., & Macfarlane, G. T. (2003) · Proceedings of the Nutrition Society · doi:10.1079/pns2002207 · Cited by 1,939

The Controversial Role of Human Gut Lachnospiraceae

Vacca, M., Celano, G., Calabrese, F. M., Portincasa, P., Gobbetti, M., & De Angelis, M. (2020) · Microorganisms · doi:10.3390/microorganisms8040573 · Cited by 1,688

Short-chain fatty acids: Linking diet, the microbiome and immunity

Mann, E. R., Lam, Y. K., & Uhlig, H. H. (2024) · Nature reviews. Immunology · doi:10.1038/s41577-024-01014-8 · Cited by 1,595

SCFA: mechanisms and functional importance in the gut

Martin‐Gallausiaux, C., Marinelli, L., Blottière, H. M., Larraufie, P., & Lapaque, N. (2020) · Proceedings of The Nutrition Society · doi:10.1017/s0029665120006916 · Cited by 1,585

Short chain fatty acids in human gut and metabolic health

Blaak, E. E., Canfora, E. E., Theis, S., Frost, G., Groen, A. K., Mithieux, G., Nauta, A., Scott, K., Stahl, B., van Harsselaar, J., et al. (2020) · Beneficial Microbes · doi:10.3920/bm2020.0057 · Cited by 1,103

The microbiome and inflammatory bowel disease

Glassner, K. L., Abraham, B. P., & Quigley, E. M. M. (2020) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2019.11.003 · Cited by 875

Butyrate and the Intestinal Epithelium: Modulation of Proliferation and Inflammation in Homeostasis and Disease

Salvi, P. S., & Cowles, R. A. (2021) · Cells · doi:10.3390/cells10071775 · Cited by 574

Review article: short chain fatty acids as potential therapeutic agents in human gastrointestinal and inflammatory disorders

Gill, P. A., van Zelm, M. C., Muir, J. G., & Gibson, P. R. (2018) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.14689 · Cited by 520

Respiratory viral infection-induced microbiome alterations and secondary bacterial pneumonia.

Hanada, S., Pirzadeh, M., Carver, K. Y., & Deng, J. C. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02640 · Cited by 495

Complex regulatory effects of gut microbial short-chain fatty acids on immune tolerance and autoimmunity

Kim, C. H. (2023) · Cellular & Molecular Immunology · doi:10.1038/s41423-023-00987-1 · Cited by 420

A Cross-Talk Between Microbiota-Derived Short-Chain Fatty Acids and the Host Mucosal Immune System Regulates Intestinal Homeostasis and Inflammatory Bowel Disease

Gonçalves, P., Araújo, J. R., & Santo, J. P. D. (2018) · Inflammatory Bowel Diseases · doi:10.1093/ibd/izx029 · Cited by 404

Immune regulation by microbiome metabolites

Kim, C. H. (2018) · Immunology · doi:10.1111/imm.12930 · Cited by 375

Organoids in immunological research

Bar-Ephraim, Y. E., Kretzschmar, K., & Clevers, H. (2020) · Nature Reviews Immunology · doi:10.1038/s41577-019-0248-y · Cited by 361

Connecting the immune system, systemic chronic inflammation and the gut microbiome: the role of sex

Rizzetto, L., Fava, F., Tuohy, K. M., & Selmi, C. (2018) · Journal of Autoimmunity · doi:10.1016/j.jaut.2018.05.008 · Cited by 331

Grains – a major source of sustainable protein for health

Poutanen, K. S., Kårlund, A., Gómez-Gallego, C., Johansson, D. P., Scheers, N., Marklinder, I., Eriksen, A. K., Silventoinen, P., Nordlund, E., Sözer, N., et al. (2021) · Nutrition Reviews · doi:10.1093/nutrit/nuab084 · Cited by 347

Compositional and Temporal Changes in the Gut Microbiome of Pediatric Ulcerative Colitis Patients Are Linked to Disease Course

Schirmer, M., Denson, L. A., Vlamakis, H. C., Franzosa, E. A., Thomas, S., Gotman, N., Rufo, P. A., Baker, S. S., Sauer, C. G., Markowitz, J. F., et al. (2018) · Cell Host & Microbe · doi:10.1016/j.chom.2018.09.009 · Cited by 292

Intestinal epithelial cells: At the interface of the microbiota and mucosal immunity

Soderholm, A. T., & Pedicord, V. A. (2019) · Immunology · doi:10.1111/imm.13117 · Cited by 281

Phenotypic landscape of intestinal organoid regeneration

Lukonin, I., Serra, D., Challet Meylan, L., Volkmann, K., Baaten, J., Zhao, R., Meeusen, S., Colman, K., Maurer, F., Stadler, M. B., et al. (2020) · Nature · doi:10.1038/s41586-020-2776-9 · Cited by 283

The functionality of prebiotics as immunostimulant: Evidences from trials on terrestrial and aquatic animals

Nawaz, A., Javaid, A. B., Irshad, S., Hoseinifar, S. H., & Xiong, H. (2018) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2018.03.004 · Cited by 248

Host- and Microbiota-Derived Extracellular Vesicles, Immune Function, and Disease Development

Macia, L., Nanan, R. K. H., Hosseini‐Beheshti, E., & Grau, G. E. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms21010107 · Cited by 241

Microbiome Dependent Regulation of Tregs and Th17 Cells in Mucosa

Pandiyan, P., Bhaskaran, N., Zou, M., Schneider, E., Jayaraman, S., & Huehn, J. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00426 · Cited by 237

Acetate differentially regulates IgA reactivity to commensal bacteria

Takeuchi, T., Miyauchi, E., Kanaya, T., Kato, T., Nakanishi, Y., Watanabe, T., Kitami, T., Taida, T., Sasaki, T., Negishi, H., et al. (2021) · Nature · doi:10.1038/s41586-021-03727-5 · Cited by 232

Vitamin D and intestinal homeostasis: Barrier, microbiota, and immune modulation

Fakhoury, H. M. A., Kvietys, P. R., Al-Kattan, W., Anouti, F. A., Elahi, M. A., Karras, S. Ν., & Grant, W. B. (2020) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2020.105663 · Cited by 212

Diversity and dynamism of IgA−microbiota interactions

Huus, K. E., Petersen, C., & Finlay, B. B. (2021) · Nature Reviews Immunology · doi:10.1038/s41577-021-00506-1 · Cited by 198

Huddling remodels gut microbiota to reduce energy requirements in a small mammal species during cold exposure

Zhang, X., Sukhchuluun, G., Bo, T., Chi, Q., Yang, J., Chen, B., Zhang, L., & Wang, D. (2018) · Microbiome · doi:10.1186/s40168-018-0473-9 · Cited by 161

The Role of Short-Chain Fatty Acids and Bile Acids in Intestinal and Liver Function, Inflammation, and Carcinogenesis

Visekruna, A., & Luu, M. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.703218 · Cited by 170

Regulation of IgA Production by Intestinal Dendritic Cells and Related Cells

Tezuka, H., & Ohteki, T. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01891 · Cited by 159

Microbiota and Food Allergy

Shu, S.-A., Yuen, A. W. T., Woo, E., Chu, K. H., Kwan, H. S., Yang, G., Yang, Y., & Leung, P. S. C. (2018) · Clinical Reviews in Allergy & Immunology · doi:10.1007/s12016-018-8723-y · Cited by 160

Detrimental Impact of Microbiota-Accessible Carbohydrate-Deprived Diet on Gut and Immune Homeostasis: An Overview

Daïen, C., Pinget, G. V., Tan, J. K., & Macia, L. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00548 · Cited by 147

Gut Microbiome as Target for Innovative Strategies Against Food Allergy

Canani, R. B., Paparo, L., Nocerino, R., Scala, C. D., Gatta, G. D., Maddalena, Y., Buono, A., Bruno, C., Voto, L., & Ercolini, D. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00191 · Cited by 145

Gut microbiota-derived metabolites tune host homeostasis fate

Kim, S., Seo, S., & Kweon, M. (2024) · Seminars in Immunopathology · doi:10.1007/s00281-024-01012-x · Cited by 156

Exploring the Molecular Mechanisms Underlying the Protective Effects of Microbial SCFAs on Intestinal Tolerance and Food Allergy

Luu, M., Monning, H., & Visekruna, A. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01225 · Cited by 139

Selenium nanoparticles in poultry feed modify gut microbiota and increase abundance of Faecalibacterium prausnitzii

Gangadoo, S., Dinev, I., Chapman, J., Hughes, R., Van, T. T. H., Moore, R. J., & Stanley, D. (2017) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-017-8688-4 · Cited by 130

Microbial Metabolites and Gut Immunology

Takeuchi, T., Nakanishi, Y., & Ohno, H. (2024) · Annual Review of Immunology · doi:10.1146/annurev-immunol-090222-102035 · Cited by 143

Deciphering interactions between the gut microbiota and the immune system via microbial cultivation and minimal microbiomes

Clavel, T., Neto, J. C. G., Lagkouvardos, I., & Ramer‐Tait, A. E. (2017) · Immunological Reviews · doi:10.1111/imr.12578 · Cited by 132

The gut microbiota, environmental factors, and links to the development of food allergy

Lee, K. H., Song, Y., Wu, W., Yu, K., & Zhang, G. (2020) · Clinical and Molecular Allergy · doi:10.1186/s12948-020-00120-x · Cited by 126

Regulation of common neurological disorders by gut microbial metabolites

Park, J., & Kim, C. H. (2021) · Experimental & Molecular Medicine · doi:10.1038/s12276-021-00703-x · Cited by 126

Impact of diet and the bacterial microbiome on the mucous barrier and immune disorders

Alemao, C. A., Budden, K. F., Gomez, H. M., Rehman, S. F., Marshall, J. E., Shukla, S. D., Donovan, C., Forster, S. C., Yang, I. A., Keely, S., et al. (2020) · Allergy · doi:10.1111/all.14548 · Cited by 110

Gluten free sourdough bread enriched with cricket flour for protein fortification: Antioxidant improvement and Volatilome characterization

Nissen, L., Samaei, S. P., Babini, E., & Gianotti, A. (2020) · Food Chemistry · doi:10.1016/j.foodchem.2020.127410 · Cited by 106

Dendritic Cell Subsets in Intestinal Immunity and Inflammation

Sun, T., Nguyen, A., & Gommerman, J. L. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.1900710 · Cited by 110

Prebiotic potential of hemp blended drinks fermented by probiotics

Nissen, L., di Carlo, E., & Gianotti, A. (2020) · Food Research International · doi:10.1016/j.foodres.2020.109029 · Cited by 102

Retinoic Acid, Leaky Gut, and Autoimmune Diseases

Abdelhamid, L., & Luo, X. (2018) · Nutrients · doi:10.3390/nu10081016 · Cited by 90

Prebiotics: Mechanisms and Preventive Effects in Allergy

Brosseau, C., Selle, A., Palmer, D. J., Prescott, S. L., Barbarot, S., & Bodinier, M. (2019) · Nutrients · doi:10.3390/nu11081841 · Cited by 100

Gut microbial metabolites alter IgA immunity in type 1 diabetes

Huang, J., Pearson, J. A., Peng, J., Hu, Y., Sha, S., Xing, Y., Huang, G., Li, X., Hu, F., Xie, Z., et al. (2020) · JCI Insight · doi:10.1172/jci.insight.135718 · Cited by 92

Gut microbial fermentation promotes the intestinal anti-inflammatory activity of Chinese yam polysaccharides

Bai, Y., Zhou, Y., Zhang, R., Chen, Y., Wang, F., & Zhang, M. (2022) · Food Chemistry · doi:10.1016/j.foodchem.2022.134003 · Cited by 90

New insights in gut microbiota and mucosal immunity of the small intestine

Million, M., Tomas, J., Wagner, C., Lelouard, H., Raoult, D., & Gorvel, J. (2018) · Human Microbiome Journal · doi:10.1016/j.humic.2018.01.004 · Cited by 85

Gut microbiota dysbiosis: The potential mechanisms by which alcohol disrupts gut and brain functions

Chen, G., Shi, F., Yin, W., Guo, Y., Liu, A., Shuai, J., & Sun, J. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.916765 · Cited by 85

Dietary Fiber from Oat and Rye Brans Ameliorate Western Diet–Induced Body Weight Gain and Hepatic Inflammation by the Modulation of Short‐Chain Fatty Acids, Bile Acids, and Tryptophan Metabolism

Kundi, Z. M., Lee, J. C., Pihlajamäki, J., Chan, C. B., Leung, K. S., So, S. S. Y., Nordlund, E., Kolehmainen, M., & El-Nezami, H. S. (2020) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201900580 · Cited by 77

Chronic opioid use modulates human enteric microbiota and intestinal barrier integrity

Cruz-Lebrón, A., Johnson, R., Mazahery, C., Troyer, Z., Joussef-Piña, S., Quiñones‐Mateu, M. E., Strauch, C., Hazen, S. L., & Levine, A. D. (2021) · Gut Microbes · doi:10.1080/19490976.2021.1946368 · Cited by 76

ROS-associated immune response and metabolism: a mechanistic approach with implication of various diseases

Banerjee, S., Ghosh, S., Mandal, A., Ghosh, N., & Sil, P. C. (2020) · Archives of Toxicology · doi:10.1007/s00204-020-02801-7 · Cited by 74

Modulatory effects of gut microbiome in cancer immunotherapy: A novel paradigm for blockade of immune checkpoint inhibitors

Rezasoltani, S., Yadegar, A., Aghdaei, H. A., & Zali, M. R. (2020) · Cancer Medicine · doi:10.1002/cam4.3694 · Cited by 67

Ginsenoside Rk3 alleviates gut microbiota dysbiosis and colonic inflammation in antibiotic-treated mice

Bai, X., Fu, R., Duan, Z., Wang, P., Zhu, C., & Fan, D. (2021) · Food Research International · doi:10.1016/j.foodres.2021.110465 · Cited by 67

The Role of Gut Microbiota and Metabolites in Obesity-Associated Chronic Gastrointestinal Disorders

Islam, M. R., Arthur, S., Haynes, J., Butts, M. R., Nepal, N., & Sundaram, U. (2022) · Nutrients · doi:10.3390/nu14030624 · Cited by 73

Pectin Interaction with Immune Receptors is Modulated by Ripening Process in Papayas

do Prado, S. B. R., Beukema, M., Jermendi, É., Schols, H. A., de Vos, P., & Fabi, J. P. (2020) · Scientific Reports · doi:10.1038/s41598-020-58311-0 · Cited by 68

Butyrate: Connecting the gut-lung axis to the management of pulmonary disorders

Corrêa, R. O., Castro, P. R., Moser, R., Ferreira, C. M., Quesniaux, V. F. J., Vinolo, M. A. R., & Ryffel, B. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.1011732 · Cited by 72

Ingestion, Immunity, and Infection: Nutrition and Viral Respiratory Tract Infections

Govers, C., Calder, P. C., Savelkoul, H. F. J., Albers, R., & van Neerven, R. J. J. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.841532 · Cited by 71

Regulation of Gastrointestinal Immunity by Metabolites

Gu, B., Kim, M., & Yun, C. (2021) · Nutrients · doi:10.3390/nu13010167 · Cited by 57

Free Fatty Acids Signature in Human Intestinal Disorders: Significant Association between Butyric Acid and Celiac Disease

Baldi, S., Menicatti, M., Nannini, G., Niccolai, E., Russo, E., Ricci, F., Pallecchi, M., Romano, F., Pedone, M., Poli, G., et al. (2021) · Nutrients · doi:10.3390/nu13030742 · Cited by 62

Respiratory and Intestinal Microbiota in Pediatric Lung Diseases—Current Evidence of the Gut–Lung Axis

Stricker, S., Hain, T., Chao, C., & Rudloff, S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23126791 · Cited by 64

Extruded sorghum (Sorghum bicolor L.) improves gut microbiota, reduces inflammation, and oxidative stress in obese rats fed a high-fat diet

de Sousa, A. R., Moreira, M. E. D. C., Grancieri, M., Toledo, R. C. L., Araújo, F. D. O., Mantovani, H. C., Queiróz, V. A. V., & Martino, H. S. D. (2019) · Journal of Functional Foods · doi:10.1016/j.jff.2019.05.009 · Cited by 54

IgA in human health and diseases: Potential regulator of commensal microbiota

Takeuchi, T., & Ohno, H. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1024330 · Cited by 53

Determination of butyric acid dosage based on clinical and experimental studies – a literature review

Banasiewicz, T., Domagalska, D., Borycka-Kiciak, K., & Rydzewska, G. M. (2020) · Gastroenterology Review · doi:10.5114/pg.2020.95556 · Cited by 51

Mucosal Barrier and Th2 Immune Responses Are Enhanced by Dietary Inulin in Pigs Infected With Trichuris suis

Myhill, L. J., Stolzenbach, S., Hansen, T. V. A., Skovgaard, K., Stensvold, C. R., Andersen, L. O., Nejsum, P. L., Mejer, H., Thamsborg, S. M., & Williams, A. R. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02557 · Cited by 51

Microbiota-derived short-chain fatty acids functions in the biology of B lymphocytes: From differentiation to antibody formation

Qu, S., Gao, Y., Ma, J., & Yan, Q. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.115773 · Cited by 52

Dysbiotic Gut Microbiota-Derived Metabolites and Their Role in Non-Communicable Diseases

Tan, J., Taitz, J., Nanan, R. K. H., Grau, G. E., & Macia, L. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242015256 · Cited by 58

A cross talk between microbial metabolites and host immunity: Its relevance for allergic diseases

Losol, P., Wolska, M., Wypych, T. P., Yao, L., O’Mahony, L., & Sokołowska, M. (2024) · Clinical and Translational Allergy · doi:10.1002/clt2.12339 · Cited by 54

Your Regulatory T Cells Are What You Eat: How Diet and Gut Microbiota Affect Regulatory T Cell Development

Tan, J., Taitz, J., Sun, S. M., Langford, L., Ni, D., & Macia, L. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.878382 · Cited by 50

Ingestion of Non-digestible Carbohydrates From Plant-Source Foods and Decreased Risk of Colorectal Cancer: A Review on the Biological Effects and the Mechanisms of Action

do Prado, S. B. R., Castro‐Alves, V., Ferreira, G. F., & Fabi, J. P. (2019) · Frontiers in Nutrition · doi:10.3389/fnut.2019.00072 · Cited by 53

Butyrate: A Link between Early Life Nutrition and Gut Microbiome in the Development of Food Allergy

Costanzo, M. D., Paulis, N. D., & Biasucci, G. (2021) · Life · doi:10.3390/life11050384 · Cited by 50

Progress towards pig nutrition in the last 27 years

Wu, Y., Zhao, J., Xu, C., Ma, N., He, T., Zhao, J., Ma, X., & Thacker, P. A. (2018) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.9095 · Cited by 49

Altered intestinal microbiota induced by chronic hypoxia drives the effects on lipid metabolism and the immune response of oriental river prawn Macrobrachium nipponense

Sun, S., Yang, M., Fu, H., Ge, X., & Zou, J. (2020) · Aquaculture · doi:10.1016/j.aquaculture.2020.735431 · Cited by 47

Gut microbiota in ALS: possible role in pathogenesis?

McCombe, P. A., Henderson, R. D., Lee, A., Lee, J. D., Woodruff, T. M., Restuadi, R., McRae, A., Wray, N. R., Ngo, S., & Steyn, F. J. (2019) · Expert Review of Neurotherapeutics · doi:10.1080/14737175.2019.1623026 · Cited by 46

The role of retinoic acid in the production of immunoglobulin A

Bos, A. V., van Egmond, M., & Mebius, R. E. (2022) · Mucosal Immunology · doi:10.1038/s41385-022-00509-8 · Cited by 48

Treatment of inflammatory bowel disease: Potential effect of NMN on intestinal barrier and gut microbiota

Huang, P., Wang, X., Wang, S., Wu, Z., Zhou, Z., Shao, G., Ren, C., Kuang, M., Zhou, Y., Jiang, A., et al. (2022) · Current Research in Food Science · doi:10.1016/j.crfs.2022.08.011 · Cited by 43

Short Chain Fatty Acids Enhance Expression and Activity of the Umami Taste Receptor in Enteroendocrine Cells via a Gαi/o Pathway

Shackley, M., Ma, Y., Tate, E. W., Brown, A., Frost, G. S., & Hanyaloglu, A. C. (2020) · Frontiers in Nutrition · doi:10.3389/fnut.2020.568991 · Cited by 43

Immunomodulatory Effects of Microbiota-Derived Short-Chain Fatty Acids in Autoimmune Liver Diseases

Zhang, W., Mackay, C. R., & Gershwin, M. E. (2023) · The Journal of Immunology · doi:10.4049/jimmunol.2300016 · Cited by 44

Microbiota-accessible carbohydrates (MACs) as novel gut microbiome modulators in noncommunicable diseases

Ayakdaş, G., & Ağagündüz, D. (2023) · Heliyon · doi:10.1016/j.heliyon.2023.e19888 · Cited by 47

Dietary Lactobacillus johnsonii -derived extracellular vesicles ameliorate acute colitis by regulating gut microbiota and maintaining intestinal barrier homeostasis

Li, Z., Li, M., Fang, X., Yu, D., & Hu, X. (2024) · Food & Function · doi:10.1039/d4fo04194a · Cited by 42

Dietary, nondigestible oligosaccharides and Bifidobacterium breve M-16V suppress allergic inflammation in intestine via targeting dendritic cell maturation

de Kivit, S., Kostadinova, A. I., Kerperien, J., Morgan, M. E., Ayechu-Muruzabal, V., Hofman, G. A., Knippels, L. M. J., Kraneveld, A. D., Garssen, J., & Willemsen, L. E. M. (2017) · Journal of Leukocyte Biology · doi:10.1189/jlb.3a0516-236r · Cited by 42

Interaction of the Gut Microbiome and Immunity in Multiple Sclerosis: Impact of Diet and Immune Therapy

Yadav, S. K., Ito, K., & Dhib-Jalbut, S. S. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241914756 · Cited by 44

The role of probiotics in prevention and treatment of food allergy

Gu, S., Yang, D. J., Liu, C., & Xue, W. (2022) · Food Science and Human Wellness · doi:10.1016/j.fshw.2022.09.001 · Cited by 47

Polymeric immunoglobulin receptor deficiency exacerbates autoimmune hepatitis by inducing intestinal dysbiosis and barrier dysfunction

Lin, H., Lin, J., Pan, T., Li, T., Jiang, H., Fang, Y., Wang, Y., Wu, F.-L., Huang, J. M., Zhang, H., et al. (2023) · Cell Death and Disease · doi:10.1038/s41419-023-05589-3 · Cited by 37

Blood and guts: how the intestinal microbiome shapes hematopoiesis and treatment of hematologic disease

Sanchez, J. F., Maknojia, A., & King, K. Y. (2024) · Blood · doi:10.1182/blood.2023021174 · Cited by 41

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