Interaction between the gut microbiome and mucosal immune system

An obesity-associated gut microbiome with increased capacity for energy harvest

Turnbaugh, P. J., Ley, R. E., Mahowald, M. A., Magrini, V., Mardis, E. R., & Gordon, J. I. (2006) · Nature · doi:10.1038/nature05414 · Cited by 12,444

A human gut microbial gene catalogue established by metagenomic sequencing

MetaHIT Consortium, Qin, J., Li, R., Raes, J., Arumugam, M., Burgdorf, K. S., Manichanh, C., Nielsen, T., Pons, N., Levenez, F., et al. (2010) · Nature · doi:10.1038/nature08821 · Cited by 11,624

Diet rapidly and reproducibly alters the human gut microbiome

David, L. A., Maurice, C. F., Carmody, R. N., Gootenberg, D. B., Button, J. E., Wolfe, B. E., Ling, A. V., Devlin, A. S., Varma, Y., Fischbach, M. A., et al. (2014) · Nature · doi:10.1038/nature12820 · Cited by 10,100

Human gut microbes associated with obesity

Ley, R. E., Turnbaugh, P. J., Klein, S., & Gordon, J. I. (2006) · Nature · doi:10.1038/4441022a · Cited by 8,785

Diversity of the Human Intestinal Microbial Flora

Eckburg, P. B., Bik, E. M., Bernstein, C. N., Purdom, E., Dethlefsen, L., Sargent, M., Gill, S. R., Nelson, K. E., & Relman, D. A. (2005) · Science · doi:10.1126/science.1110591 · Cited by 7,913

A metagenome-wide association study of gut microbiota in type 2 diabetes

Qin, J., Li, Y., Cai, Z., Li, S., Zhu, J., Zhang, F., Liang, S., Zhang, W., Guan, Y., Shen, D., et al. (2012) · Nature · doi:10.1038/nature11450 · Cited by 6,762

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

Smith, P. M., Howitt, M. R., Panikov, N., Michaud, M., Gallini, C. A., Bohlooly-Y, M., Glickman, J. N., & Garrett, W. S. (2013) · Science · doi:10.1126/science.1241165 · Cited by 5,413

Toll-like receptors: critical proteins linking innate and acquired immunity

Akira, S., Takeda, K., & Kaisho, T. (2001) · Nature Immunology · doi:10.1038/90609 · Cited by 4,777

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

Frank, D. N., St. Amand, A. L., Feldman, R. A., Boedeker, E. C., Harpaz, N., & Pace, N. R. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0706625104 · Cited by 4,611

Induction of Intestinal Th17 Cells by Segmented Filamentous Bacteria

Ivanov, I. I., Atarashi, K., Manel, N., Brodie, E. L., Shima, T., Karaoz, U., Wei, D., Goldfarb, K. C., Santee, C. A., Lynch, S. V., et al. (2009) · Cell · doi:10.1016/j.cell.2009.09.033 · Cited by 4,554

Antibiotic and antifungal use in pediatric leukemia and lymphoma patients are associated with increasing opportunistic pathogens and decreasing bacteria responsible for activities that enhance colonic defense

Dunn, K. A., MacDonald, T., Rodrigues, G. J., Forbrigger, Z., Bielawski, J. P., Langille, M. G. I., Limbergen, J. V., & Kulkarni, K. P. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.924707 · Cited by 21

Dietary Supplementation with Black Raspberries Altered the Gut Microbiome Composition in a Mouse Model of Colitis-Associated Colorectal Cancer, although with Differing Effects for a Healthy versus a Western Basal Diet

Rodriguez, D. M., Hintze, K. J., Rompato, G., Wettere, A. J. V., Ward, R. E., Phatak, S., Neal, C., Armbrust, T., Stewart, E. C., Thomas, A. J., et al. (2022) · Nutrients · doi:10.3390/nu14245270 · Cited by 23

Zhizhu decoction alleviates slow transit constipation by regulating aryl hydrocarbon receptor through gut microbiota

Wen, Y., Zhan, Y., Tang, S., Liu, F., Wu, R., Kong, P., Li, Q., & Tang, X. (2022) · Pharmaceutical Biology · doi:10.1080/13880209.2022.2157020 · Cited by 23

Gut microbiome composition associates with corticosteroid treatment, morbidity, and senescence in Chinook salmon (Oncorhynchus tshawytscha)

Couch, C. E., Neal, W. T., Herron, C. L., Kent, M. L., Schreck, C. B., & Peterson, J. T. (2023) · Scientific Reports · doi:10.1038/s41598-023-29663-0 · Cited by 20

Gut microbiome associated dysbiosis: Limited regimens and expanding horizons of phage therapy

Singha, B., Rawat, B. S., Venkataraman, R., Nair, T., Rosenn, E. H., & Soni, V. (2023) · Aspects of Molecular Medicine · doi:10.1016/j.amolm.2023.100029 · Cited by 23

Maternal-Foetal/Infant Interactions—Gut Microbiota and Immune Health

Adamczak, A. M., Werblińska, A., Jamka, M., & Walkowiak, J. (2024) · Biomedicines · doi:10.3390/biomedicines12030490 · Cited by 24

The effect of lentinan on dexamethasone-induced immunosuppression in mice

Jiao, L., Jin, H., Song, Z., Wang, Z., Yu, L. C., Yu, R., Wang, D., Gao, Q., Peng, S., Sun, H., et al. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.130621 · Cited by 21

Fecal microbiota transplantation for graft-versus-host disease in children and adults: methods, clinical effects, safety

Goloshchapov, O. V., Чухловин, А. Б., Bakin, E. A., Stanevich, O. V., Klementeva, R. V., Щербаков, А. А., Shvetsov, A. N., Suvorova, M. A., Bondarenko, S. N., Kucher, М. A., et al. (2020) · Terapevticheskii arkhiv · doi:10.26442/00403660.2020.07.000773 · Cited by 21

Sustainable diets with plant-based proteins require considerations for prevention of proteolytic fermentation

Boven, L. G., Akkerman, R., & de Vos, P. (2024) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2024.2352523 · Cited by 20

Polystyrene nanoplastics alter intestinal toxicity of 2,4-DTBP in a sex-dependent manner in zebrafish (Danio rerio)

Liu, R., Gao, H., Liang, X., Zhang, J., Meng, Q., Wang, Y., Guo, W., Martyniuk, C. J., & Zha, J. (2024) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2024.135585 · Cited by 20

Analyzing human gut microbiome data from global populations: challenges and resources

Arif, S. J., Graham, S. P., Abdill, R. J., & Blekhman, R. (2025) · Trends in Microbiology · doi:10.1016/j.tim.2025.05.008 · Cited by 24

Xiaoyaosan improves depression-like behaviours in mice with post-stroke depression by modulating gut microbiota and microbial metabolism and regulating P2X7R/NLRP3 inflammasome

Chen, Y.-Y., Lu, Y., Wang, Y.-D., Ding, N.-N., Huang, Z.-X., Hu, J.-B., Tong, J.-X., Zhang, Y.-R., Deng, L., Luo, X., et al. (2025) · Phytomedicine · doi:10.1016/j.phymed.2025.157078 · Cited by 20

Immune cells: the key mediator between the gut microbiota and osteoporosis

Ma, T., Zhang, T., Peng, C., Liu, K., Xiong, Y., Chen, K., Peng, N., Wei, Z., Kuang, J., & Ou, L. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1680021 · Cited by 22

Multi-omic Profiling Reveals that Intra-abdominal-Hypertension-Induced Intestinal Damage Can Be Prevented by Microbiome and Metabolic Modulations with 5-Hydroxyindoleacetic Acid as a Diagnostic Marker

Li, F., Jiang, L., Pan, S., Jiang, S., Fan, Y., Jiang, C., Gao, C., & Leng, Y. (2022) · mSystems · doi:10.1128/msystems.01204-21 · Cited by 21

Gut microbiota-dependent trimethylamine n-oxide pathway contributes to the bidirectional relationship between intestinal inflammation and periodontitis

Wang, Q., Sun, Y., Zhou, T., Jiang, C., Lan, A., & Xu, W. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.1125463 · Cited by 23

Structure-function relationship and impact on the gut-immune barrier function of non-digestible carbohydrates and human milk oligosaccharides applicable for infant formula

Chen, X., & de Vos, P. (2023) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2023.2199072 · Cited by 23

The Potential of Probiotics as Ingestible Adjuvants and Immune Modulators for Antiviral Immunity and Management of SARS-CoV-2 Infection and COVID-19

Tomkinson, S., Triscott, C., Schenk, E., & Foey, A. (2023) · Pathogens · doi:10.3390/pathogens12070928 · Cited by 24

Chicoric Acid Effectively Mitigated Dextran Sulfate Sodium (DSS)-Induced Colitis in BALB/c Mice by Modulating the Gut Microbiota and Fecal Metabolites

Yang, J., Jie, L., Gu, T., Sun, Q., Xu, W., & Peng, Y. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25020841 · Cited by 20

Polysaccharide Isolated from Agaricus blazei Murill Alleviates Intestinal Ischemia/Reperfusion Injury through Regulating Gut Microbiota and Mitigating Inflammation in Mice

Zhao, M., Tang, F., Huang, X., Ma, J., Wang, F., & Zhang, P. (2024) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.3c08482 · Cited by 20

Microbiota in tumors: new factor influencing cancer development

Jiang, H., Li, L., Bao, Y., Cao, X., & Ma, L. (2024) · Cancer Gene Therapy · doi:10.1038/s41417-024-00833-0 · Cited by 24

Gut microbiota: One of the new frontiers for elucidating fundamentals of Vipaka in Ayurveda

Pawar, S. D., Ranade, A., & Shirolkar, A. R. (2019) · AYU (An International Quarterly Journal of Research in Ayurveda) · doi:10.4103/ayu.ayu_210_18 · Cited by 19

Polysaccharides from Shiitake Culinary-Medicinal Mushroom Lentinus edodes (Agaricomycetes) Suppress pMLKL-Mediated Necroptotic Cell Death and Colitis in Mice

Alagbaoso, C. A., & Mizuno, M. (2021) · International journal of medicinal mushrooms · doi:10.1615/intjmedmushrooms.2021038850 · Cited by 19

The role of mediterranean diet and gut microbiota in type- diabetes mellitus associated with obesity (diabesity)

Özsoy, S., Sultanoğlu, N., & Şanlıdağ, T. (2022) · Journal of preventive medicine and hygiene · doi:10.15167/2421-4248/jpmh2022.63.2s3.2751 · Cited by 21

Pueraria lobata polysaccharides alleviate neonatal calf diarrhea by modulating gut microbiota and metabolites

Shen, L., Shen, Y. M., Zhu, Y., You, L., Zhang, Y., 苏柘僮, Deng, J., Deng, J., Zuo, Z., Zhong, Z., et al. (2023) · Frontiers in Veterinary Science · doi:10.3389/fvets.2022.1024392 · Cited by 22

Piezo1 in Digestive System Function and Dysfunction

He, J., Xie, X., Xiao, Z., Qian, W., Zhang, L., & Hou, X. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241612953 · Cited by 21

The Impact of Antibiotics and Steroids on the Nasal Microbiome in Patients with Chronic Rhinosinusitis: A Systematic Review According to PICO Criteria

Loperfido, A., Cavaliere, C., Begvarfaj, E., Ciofalo, A., D’Erme, G., VINCENTIIS, M. D., Greco, A., Millarelli, S., Bellocchi, G., & Masieri, S. (2023) · Journal of Personalized Medicine · doi:10.3390/jpm13111583 · Cited by 22

MinION Sequencing of colorectal cancer tumour microbiomes—A comparison with amplicon-based and RNA-Sequencing

Taylor, W. S., Pearson, J. F., Miller, A. L., Schmeier, S., Frizelle, F., & Purcell, R. V. (2020) · PLoS ONE · doi:10.1371/journal.pone.0233170 · Cited by 18

Exploring the role of gut microbiota in obesity and PCOS: Current updates and future prospects

Zhang, H., Butoyi, C., Yuan, G., & Jia, J. (2023) · Diabetes Research and Clinical Practice · doi:10.1016/j.diabres.2023.110781 · Cited by 20

HIV-associated neurocognitive disorder: key implications of the microbiota-gut-brain axis

Hu, A., Zaongo, S. D., Harypursat, V., Wang, X., Ouyang, J., & Chen, Y. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1428239 · Cited by 18

Comparative gut microbiome research through the lens of ecology: theoretical considerations and best practices

Degregori, S., Wang, X., Kommala, A., Schulhof, N., Moradi, S., MacDonald, A., Eblen, K., Jukovich, S., Smith, E., Kelleher, E., et al. (2024) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.13161 · Cited by 19

Influence of selected dosages of plastic microparticles on the porcine fecal microbiome

Gałęcka, I., Rychlik, A., & Całka, J. (2025) · Scientific Reports · doi:10.1038/s41598-024-80337-x · Cited by 20

Bacteroides Fragilis Transplantation Reverses Reproductive Senescence by Transporting Extracellular Vesicles Through the Gut‐Ovary Axis

Xiong, Y., Lu, X., Li, B., Xu, S. S., Fu, B., Sha, Z., Tian, R., Yao, R., Li, Q., Yan, J., et al. (2025) · Advanced Science · doi:10.1002/advs.202409740 · Cited by 18

The Impact of a Dried Fruit and Vegetable Supplement and Fiber Rich Shake on Gut and Health Parameters in Female Healthcare Workers: A Placebo-Controlled, Double-Blind, Randomized Clinical Trial

van der Merwe, M., Moore, D., Hill, J. L., Keating, F. H., Buddington, R. K., Bloomer, R. J., Wang, A., & Bowman, D. D. (2021) · Microorganisms · doi:10.3390/microorganisms9040843 · Cited by 18

Donor age and body weight determine the effects of fecal microbiota transplantation on growth performance, and fecal microbiota development in recipient pigs

Wang, X., Tsai, T.-C., Zuo, B., Wei, X., Deng, F., Li, Y., Maxwell, C. V. V., Yang, H., Xiao, Y., & Zhao, J. (2022) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-022-00696-1 · Cited by 18

The Role of the Microbiome in First Episode of Psychosis

Nuncio-Mora, L., Lanzagorta, N., Nicolini, H., Sarmiento, E., Ortiz, G., Sosa, F., & Mendoza, A. D. G. (2023) · Biomedicines · doi:10.3390/biomedicines11061770 · Cited by 18

The Potential Effects of Isoleucine Restricted Diet on Cognitive Impairment in High‐Fat‐Induced Obese Mice via Gut Microbiota–Brain Axis

Wang, Y., Rong, X., Guan, H., Ouyang, F., Zhou, X., Li, F., Tan, X., & Li, D. (2023) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202200767 · Cited by 18

In vitro fermentation of kodo and kutki millets by human gut microbiota: Gut microbiota and metabolomic analysis

Sori, N., Poyil, N. C., & Khan, M. (2023) · Food Bioscience · doi:10.1016/j.fbio.2023.103343 · Cited by 18

Alterations of the gut microbiota in the lupus nephritis: a systematic review

Wang, A., Zhao, J., Qin, Y., Zhang, Y., Xing, Y., Wang, Y., Yu, Z., Yan, J., Han, M., Yuan, J., et al. (2023) · Renal Failure · doi:10.1080/0886022x.2023.2285877 · Cited by 18

The Role of Gut Microbiota in Overcoming Resistance to Checkpoint Inhibitors in Cancer Patients: Mechanisms and Challenges

Bouferraa, Y., Chedid, A., Amhaz, G., Lakkiss, A. E., Mukherji, D., Temraz, S. N., & Shamseddine, A. I. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22158036 · Cited by 18

Impact of the gut microbiota on the immune system

Kogut, M. H. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-818708-1.00017-8 · Cited by 19

The microbiome compositional and functional differences between rectal mucosa and feces

Yin, X.-F., Ye, T., Chen, H., Liu, J., Mu, X.-F., Li, H., Wang, J., Yuanjia, H., Cao, H., & Kang, W. (2024) · Microbiology Spectrum · doi:10.1128/spectrum.03549-23 · Cited by 20

Hirschsprung-associated enterocolitis: a comprehensive review

Ziogas, I. A., Kuruvilla, K. P., Fu, M., & Gosain, A. (2024) · World Journal of Pediatric Surgery · doi:10.1136/wjps-2024-000878 · Cited by 17

Organic side streams: using microbes to make substrates more fit for mass producing insects for use as feed

Zhang, J. B., Yu, Y. Q., Tomberlin, J. K., Cai, M., Zheng, L., & Yu, Z. (2021) · Journal of Insects as Food and Feed · doi:10.3920/jiff2020.0078 · Cited by 17

Bioactivities of Dietary Polyphenols and Their Effects on Intestinal Microbiota

Cui, Q., Zhang, X., Shao, J., Ni, W., Yang, Y., & Yan, B. (2022) · Mini-Reviews in Medicinal Chemistry · doi:10.2174/1389557522666220811123115 · Cited by 17

The Structural Characterization and Immunomodulatory Activity of Polysaccharides from Pleurotus abieticola Fruiting Bodies

Pan, M., Kong, F., Xing, L., Yao, L., Li, Y., Liu, Y., Li, C., & Li, L. (2022) · Nutrients · doi:10.3390/nu14204410 · Cited by 17

Risk of Parkinson disease associated with pesticide exposure and protection by probiotics

Rajawat, N. K., Bhardwaj, K., & Mathur, N. (2022) · Materials Today Proceedings · doi:10.1016/j.matpr.2022.12.153 · Cited by 17

Acer truncatum leaves extract modulates gut microbiota, improves antioxidant capacity, and alleviates lipopolysaccharide-induced inflammation in broilers

Liu, J., Liang, S., Qin, K., Jia, B., Ren, Z., Yang, X., & Yang, X. (2023) · Poultry Science · doi:10.1016/j.psj.2023.102951 · Cited by 17

Evaluation of stimbiotic on growth performance and intestinal development of broilers fed corn- or wheat-based diets

Ren, Y., Tian, Y., Hou, M., Zhao, Y., Li, J., Aftab, U., Rousseau, X., Jiang, R., Kang, X., Tian, Y., et al. (2023) · Poultry Science · doi:10.1016/j.psj.2023.103094 · Cited by 17

ASTRAGALOSIDE Ⅳ MODULATES GUT MACROPHAGES M1/M2 POLARIZATION BY RESHAPING GUT MICROBIOTA AND SHORT CHAIN FATTY ACIDS IN SEPSIS

Yang, T., Xie, S., Cao, L., Li, M., Ding, L., Wang, L., Pang, S., Wang, Z., & Geng, L. (2023) · Shock · doi:10.1097/shk.0000000000002262 · Cited by 17

Causal relationship between gut microbiota and immune thrombocytopenia: a Mendelian randomization study of two samples

Guo, D., Chen, Q., Wang, G., & Li, C. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1190866 · Cited by 17

Ovarian Cancer and the Microbiome: Connecting the Dots for Early Diagnosis and Therapeutic Innovations—A Review

Choi, S.-Y., & Choi, J. (2024) · Medicina · doi:10.3390/medicina60030516 · Cited by 17

Polyphenolic Compounds: Orchestrating Intestinal Microbiota Harmony during Aging

Pereira, Q. C., Fortunato, I. M., Oliveira, F. D. S., Alvarez, M. C., dos Santos, T. W., & Ribeiro, M. L. (2024) · Nutrients · doi:10.3390/nu16071066 · Cited by 19

Potential role of the intratumoral microbiota in colorectal cancer immunotherapy

Fan, S., Zhang, W., Zhou, L., Wang, D., & Tang, D. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.112537 · Cited by 16

Effects of dietary Lactobacillus postbiotics and bacitracin on the modulation of mucosa-associated microbiota and pattern recognition receptors affecting immunocompetence of jejunal mucosa in pigs challenged with enterotoxigenic F18+ Escherichia coli

Duarte, M. E., Deng, Z., & Kim, S. W. (2024) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-024-01098-1 · Cited by 20

Gut microbiome and metabolomics in systemic sclerosis: feature, link and mechanisms

Yao, Q., Tan, W., & Bai, F. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1475528 · Cited by 17

Nutrition-Based Management of Inflammaging in CKD and Renal Replacement Therapies

Losappio, V., Infante, B., Leo, S., Troise, D. E., Calvaruso, M., Vitale, P., Renzi, S., Stallone, G., & Castellano, G. (2021) · Nutrients · doi:10.3390/nu13010267 · Cited by 19

Use of Organ Dysfunction as a Primary Outcome Variable Following Cecal Ligation and Puncture: Recommendations for Future Studies

Abraham, M. N., KELLY, A. P., Brandwein, A. B., Fernandes, T., Leisman, D. E., Taylor, M. D., Brewer, M. R., Capone, C. A., & Deutschman, C. S. (2019) · Shock · doi:10.1097/shk.0000000000001485 · Cited by 15

Deciphering the interdependent labyrinth between gut microbiota and the immune system

Saini, A., Dalal, P., & Sharma, D. (2022) · Letters in Applied Microbiology · doi:10.1111/lam.13775 · Cited by 18

Involvement of the Intestinal Microbiota in the Appearance of Multiple Sclerosis: Aloe vera and Citrus bergamia as Potential Candidates for Intestinal Health

Maiuolo, J., Musolino, V., Gliozzi, M., Carresi, C., Scarano, F., Nucera, S., Scicchitano, M., Oppedisano, F., Bosco, F., Macrì, R., et al. (2022) · Nutrients · doi:10.3390/nu14132711 · Cited by 16

Drug-Induced Enterocolitis Syndrome in Children

Filippo, P. D., Venanzi, A., Ciarelli, F., Panetti, B., Pillo, S. D., Chiarelli, F., & Attanasi, M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24097880 · Cited by 16

Beneficial Effects of Daily Consumption of Garlic and Onion Extract Concentrate on Infectious Respiratory Diseases in Elderly Resident Volunteers

García-García, J., Gracián, C., Baños, A., Guillamón, E., Gálvez, J., Rodríguez‐Nogales, A., & Fonollá, J. (2023) · Nutrients · doi:10.3390/nu15102308 · Cited by 16

Review: Effect of Experimental Diets on the Microbiome of Productive Animals

Huaiquipán, R., Quiñones, J., Díaz, R., Velásquez, C., Sepúlveda, G., Velázquez, L., Paz, E. A., Tapía, D., Cancino, D., & Sepúlveda, N. (2023) · Microorganisms · doi:10.3390/microorganisms11092219 · Cited by 16

The effects of whole grain cereals on tryptophan metabolism and intestinal barrier function: underlying factors of health impact

Liikonen, V., Gómez-Gallego, C., & Kolehmainen, M. (2023) · Proceedings of The Nutrition Society · doi:10.1017/s0029665123003671 · Cited by 15

Dietary sanguinarine supplementation improves the growth performance and intestinal immunity of broilers

Su, Y., Chang, G., Liu, J., Huang, P., & Zeng, J. (2024) · Animal nutrition · doi:10.1016/j.aninu.2024.05.009 · Cited by 18

Protective Role of Somatostatin in Sepsis-Induced Intestinal Barrier Dysfunction through Inhibiting the Activation of NF-κB Pathway

Xu, X., Zhu, Q., Li, G., Ma, J., Pan, Z., & Wu, W. (2020) · Gastroenterology Research and Practice · doi:10.1155/2020/2549486 · Cited by 16

Metagenomic Sequencing Analysis of the Effects of Colistin Sulfate on the Pig Gut Microbiome

Guo, L. J., Zhang, D., Fu, S., Zhang, J., Zhang, X., He, J., Peng, C., Zhang, Y., Qiu, Y., Ye, C., et al. (2021) · Frontiers in Veterinary Science · doi:10.3389/fvets.2021.663820 · Cited by 16

Pharmacological potential of natural medicine Astragali Radix in treating intestinal diseases

Wei, X., Leng, X., Liang, J., Liu, J., Chi, L., Deng, H., & Sun, D. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.117580 · Cited by 15

Lactobacillus murinus ZNL-13 Modulates Intestinal Barrier Damage and Gut Microbiota in Cyclophosphamide-Induced Immunosuppressed Mice

Dong, Y., Zhang, L., Qiu, D., Yao, R., Jia, H., Wang, H., Zhou, L., Zhang, J., & Zhang, N. (2025) · Foods · doi:10.3390/foods14081416 · Cited by 15

Human microbiota influence the immune cell composition and gene expression in the tumor environment of a murine model of glioma

Green, G. B. H., Cox-Holmes, A. N., Marlow, G. H., Potier, A. C. E., Wang, Y., Zhou, L., Chen, D., Morrow, C. D., & McFarland, B. C. (2025) · Gut Microbes · doi:10.1080/19490976.2025.2508432 · Cited by 15

Folic acid attenuates chronic visceral pain by reducing clostridiales abundance and hydrogen sulfide production

Weng, R., Wei, Y., Li, Y., Xu, X., Zhuang, J.-B., Xu, G.-Y., & Li, R. P. (2022) · Molecular Pain · doi:10.1177/17448069221149834 · Cited by 15

Mahuang Fuzi Xixin decoction ameliorates allergic rhinitis and repairs the airway epithelial barrier by modulating the lung microbiota dysbiosis

Wei, X., Ding, M., Xiao, L., Zhang, B., Tan, X., & Zheng, Z. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1206454 · Cited by 15

Mechanism-guided fine-tuned microbiome potentiates anti-tumor immunity in HCC

Liu, T., Guo, Y., Liao, Y., & Liu, J. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1333864 · Cited by 16

The role of intestinal microecology in inflammatory bowel disease and colorectal cancer: A review

Li, H., Wang, K., Hao, M., Liu, Y., Liang, X., Yuan, D., & Ding, L. (2023) · Medicine · doi:10.1097/md.0000000000036590 · Cited by 16

Chronic Gut Inflammation and Dysbiosis in IBS: Unraveling Their Contribution to Atopic Dermatitis Progression

Jang, J., Jang, S.-Y., Ahn, S., Oh, J., Yeom, M., Ko, S., Park, J.-W., Kwon, S.-K., Kim, K., Lee, I., et al. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25052753 · Cited by 14

Rosa roxburghii Tratt (Cili) has a more effective capacity in alleviating DSS-induced colitis compared to Vitamin C through B cell receptor pathway

Li, X., Wang, Q., Wang, F., Jin, Q., Deng, B., Yang, R., Fu, A., Li, F., Zhang, Q., & Li, F. (2024) · Food Research International · doi:10.1016/j.foodres.2024.114950 · Cited by 16

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Copper-induced sublethal effects in Bufo gargarizans tadpoles: growth, intestinal histology and microbial alternations

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Longitudinal Analysis of the Impacts of Urogenital Schistosomiasis on the Gut microbiota of Adolescents in NigeriaPreprint

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Bile acids supplementation improves colonic mucosal barrier via alteration of bile acids metabolism and gut microbiota composition in goats with subacute ruminal acidosis (SARA)

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Interactions between microbiota and innate immunity in tumor microenvironment: Novel insights into cancer progression and immunotherapy

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Combination of Lactobacillus plantarum improves the effects of tacrolimus on colitis in a mouse model

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Gut microbiota and serum metabolome reveal the mechanism by which TCM polysaccharides alleviate salpingitis in laying hens challenged by bacteria

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Oligo/polysaccharides from Cyathula officinalis and Achyranthes bidentata: a review of structures and bioactivities

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Mendelian randomization analysis reveals an independent causal relationship between four gut microbes and acne vulgaris

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The impacts of obesity in rheumatoid arthritis and insights into therapeutic purinergic modulation

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Microbiome dysbiosis in patients with chronic endometritis and Clostridium tyrobutyricum ameliorates chronic endometritis in mice

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Microbiota‐immune‐brain interactions: A new vision in the understanding of periodontal health and disease

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Exploring the gut microbiome and head and neck cancer interplay

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Androgen deficiency-induced loss of Lactobacillus salivarius extracellular vesicles is associated with the pathogenesis of osteoporosis

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Mutual Interactions Between Microbiota and the Human Immune System During the First 1000 Days of Life

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Protease Hydrolysates Ameliorates Inflammation and Intestinal Flora Imbalance in DSS-Induced Colitis Mice

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Role of the gut microbiota in airway immunity and host defense against respiratory infections

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Low-Dose Interleukin-2 Altered Gut Microbiota and Ameliorated Collagen-Induced Arthritis

Li, N., Li, X., Su, R. J., Wu, R., Niu, H.-Q., Luo, J., Gao, C., Li, X., & Wang, C. (2022) · Journal of Inflammation Research · doi:10.2147/jir.s344393 · Cited by 15

Characterization of gut microbiota in patients with stage 3–4 chronic kidney disease: a retrospective cohort study

Yang, X., Cai, S., Gong, J., Zhang, J., Lian, M., Chen, R., Zhou, L., Bai, P., Liu, B., Zhuang, M., et al. (2023) · International Urology and Nephrology · doi:10.1007/s11255-023-03893-7 · Cited by 14

Host and Graft Factors Impacting Infection Risk in Hematopoietic Cell Transplantation

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The Multifaceted Effects of Gut Microbiota on the Immune System of the Intestinal Mucosa

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Gut microbiota as a key regulator of intestinal mucosal immunity

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Microbiota–immune system interaction: an uneasy alliance

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The Role of Microbiota on the Gut Immunology

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Commensal microbiome and gastrointestinal mucosal immunity: Harmony and conflict with our closest neighbor

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