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Journal articles on the topic 'Gut micobiota and immunity'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

Eman, A. Abdelnaby, F. Mohamed Mostafa, and A.-K. Gammaz Hatem. "Pharmacological studies of feed additives (Sanguinarine and Saccharomyces cerevisiae) on growth performance, haematological and intestinal bacterial count with challenge test by Aeromonas hydrophila in Cyprinus carpio." Global Animal Science Journal 1, no. 1 (2013): 1154–72. https://doi.org/10.5281/zenodo.19336.

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This study analyzed the effect of dietary supplementation of commercial product Sangrovit<sup>® </sup>which containing the isoquinoline alkaloid sanguinarine  by 500 gm/ton ration, and <em>Saccharomyces cerevisiae</em> (yeast probiotic) by 5 g/Kg on common carp (<em>Cyprinus carpio</em>) growth performance, hematological and gut microbiota with challenge test by <em>Aeromonas hydrophila</em> in <em>Cyprinus carpio</em> compared to the control group determined at 15 days intervals during the feeding trial. Each dietary treatment had two replicate aquaria. The results showed that during

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2

Vijay-Kumar, Matam, Benoit Chassaing, Manish Kumar, MarkT Baker, and Vishal Singh. "Mammalian gut immunity." Biomedical Journal 37, no. 5 (2014): 246. http://dx.doi.org/10.4103/2319-4170.130922.

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3

Trivedi, Palak J., and David H. Adams. "Gut–liver immunity." Journal of Hepatology 64, no. 5 (2016): 1187–89. http://dx.doi.org/10.1016/j.jhep.2015.12.002.

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4

Char, Shobha, and Michael J. G. Farthing. "Bacteria and gut immunity." Current Opinion in Gastroenterology 10, no. 6 (1994): 659–63. http://dx.doi.org/10.1097/00001574-199411000-00015.

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5

Fukatsu, Kazuhiko, and Kenneth A. Kudsk. "Nutrition and Gut Immunity." Surgical Clinics of North America 91, no. 4 (2011): 755–70. http://dx.doi.org/10.1016/j.suc.2011.04.007.

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6

Velikova, Tsvetelina, Issa El Kaouri, Konstantina Bakopoulou, et al. "Mucosal Immunity and Trained Innate Immunity of the Gut." Gastroenterology Insights 15, no. 3 (2024): 661–75. http://dx.doi.org/10.3390/gastroent15030048.

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Mucosal immunity and trained innate immunity of the gut play a pivotal role in maintaining intestinal homeostasis and defending against microbial pathogens. This review provides an overview of the mechanisms underlying mucosal immunity and the concept of trained innate immunity in the gut. We discuss the interaction between gut microbiota and the host immune system, highlighting the role of epithelial cells, dendritic cells, and innate lymphoid cells, as well as the novel concept of trained innate immunity and its role in perpetuating or attenuating gut inflammation. We also comment on the cur

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7

Yadav, Sudhir Kumar, Kouichi Ito, and Suhayl Dhib-Jalbut. "Interaction of the Gut Microbiome and Immunity in Multiple Sclerosis: Impact of Diet and Immune Therapy." International Journal of Molecular Sciences 24, no. 19 (2023): 14756. http://dx.doi.org/10.3390/ijms241914756.

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The bidirectional communication between the gut and central nervous system (CNS) through microbiota is known as the microbiota–gut–brain axis. The brain, through the enteric neural innervation and the vagus nerve, influences the gut physiological activities (motility, mucin, and peptide secretion), as well as the development of the mucosal immune system. Conversely, the gut can influence the CNS via intestinal microbiota, its metabolites, and gut-homing immune cells. Growing evidence suggests that gut immunity is critically involved in gut–brain communication during health and diseases, includ

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8

Mulder, I., B. Schmidt, R. Aminov, and D. Kelly. "Gut Health, Microbiota and Immunity." Recent Advances in Animal Nutrition 2008, no. 1 (2009): 195–210. http://dx.doi.org/10.5661/recadv-08-195.

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9

Kanellopoulos, Jean. "Mammalian gut microbiota and immunity." Biomedical Journal 37, no. 5 (2014): 245. http://dx.doi.org/10.4103/2319-4170.142419.

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10

Силивончик, Н. Н. "The Gut Microbiota and Immunity." Рецепт, no. 3 (November 10, 2021): 323–31. http://dx.doi.org/10.34883/pi.2021.24.3.002.

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Микробиота желудочно-кишечного тракта (ЖКТ) состоит из динамичного многовидового сообщества, живущего в определенной нише во взаимной синергии с организмом-хозяином. Недавние результаты показали роль микробиоты ЖКТ в модуляции иммунитета хозяина и развитии и прогрессировании заболеваний. Пробиотики определяются как живые микроорганизмы, которые при их назначении в адекватных количествах приносят пользу для здоровья хозяина. Среди прочего пробиотики имеют иммуномодулирующие свойства, которые обычно реализуются непосредственно, увеличивая активность макрофагов или естественных клетоккиллеров, мо

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11

Da Silva, Kevin. "Gut bugs alter antiviral immunity." Nature Medicine 18, no. 8 (2012): 1193. http://dx.doi.org/10.1038/nm.2908.

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12

Khamsi, Roxanne. "A gut feeling about immunity." Nature Medicine 21, no. 7 (2015): 674–76. http://dx.doi.org/10.1038/nm.3906.

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13

Viswanathan, V. K., and Gail Hecht. "Innate immunity and the gut." Current Opinion in Gastroenterology 16, no. 6 (2000): 546–51. http://dx.doi.org/10.1097/00001574-200011000-00015.

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14

Mueller, Kristen L. "Neural inputs shape gut immunity." Science 353, no. 6299 (2016): 554.2–554. http://dx.doi.org/10.1126/science.353.6299.554-b.

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15

Inglis, George Andrew S. "Enteric neurons and gut immunity." Nature Neuroscience 27, no. 12 (2024): 2269. https://doi.org/10.1038/s41593-024-01841-x.

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16

Gronke, Konrad, and Andreas Diefenbach. "Innate immunity repairs gut lining." Nature 528, no. 7583 (2015): 488–89. http://dx.doi.org/10.1038/nature16325.

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17

Dhawan, Shobhit, Cathy Cailotto, Lucien F. Harthoorn, and Wouter J. de Jonge. "Cholinergic signalling in gut immunity." Life Sciences 91, no. 21-22 (2012): 1038–42. http://dx.doi.org/10.1016/j.lfs.2012.04.042.

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18

Floch, Martin H. "Nutrition, Gut Microbiota, and Immunity." Journal of Clinical Gastroenterology 49, no. 3 (2015): 263. http://dx.doi.org/10.1097/mcg.0000000000000289.

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19

Sanidad, Katherine Z., and Melody Y. Zeng. "Neonatal gut microbiome and immunity." Current Opinion in Microbiology 56 (August 2020): 30–37. http://dx.doi.org/10.1016/j.mib.2020.05.011.

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20

Stoll, Matthew L. "Gut microbes, immunity, and spondyloarthritis." Clinical Immunology 159, no. 2 (2015): 134–42. http://dx.doi.org/10.1016/j.clim.2015.05.001.

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21

Santoni, Matteo, Francesca Miccini, and Nicola Battelli. "Gut microbiota, immunity and pain." Immunology Letters 229 (January 2021): 44–47. http://dx.doi.org/10.1016/j.imlet.2020.11.010.

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22

de Jonge, W. "Nervous modulation of gut immunity." Brain, Behavior, and Immunity 24 (August 2010): S49. http://dx.doi.org/10.1016/j.bbi.2010.07.162.

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23

Bird, Lucy. "Gut bacteria support antiviral immunity." Nature Reviews Immunology 20, no. 9 (2020): 520–21. http://dx.doi.org/10.1038/s41577-020-00412-y.

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24

Wu, Kai, Bing Yang, Wuren Huang, Leonard Dobens, Hongsheng Song, and Erjun Ling. "Gut immunity in Lepidopteran insects." Developmental & Comparative Immunology 64 (November 2016): 65–74. http://dx.doi.org/10.1016/j.dci.2016.02.010.

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25

Cummings, John H., Jean-Michel Antoine, Fernando Azpiroz, et al. "PASSCLAIM1?Gut health and immunity." European Journal of Nutrition 43, S2 (2004): ii118—ii173. http://dx.doi.org/10.1007/s00394-004-1205-4.

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26

Mendis, Mihiri, Estelle Leclerc, and Senay Simsek. "Arabinoxylans, gut microbiota and immunity." Carbohydrate Polymers 139 (March 2016): 159–66. http://dx.doi.org/10.1016/j.carbpol.2015.11.068.

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27

Zuo, Tao. "Gut bacteriophages ignite mammalian immunity." Nature Reviews Microbiology 21, no. 10 (2023): 634. http://dx.doi.org/10.1038/s41579-023-00911-4.

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28

Wang, Xinzhou, Peng Zhang, and Xin Zhang. "Probiotics Regulate Gut Microbiota: An Effective Method to Improve Immunity." Molecules 26, no. 19 (2021): 6076. http://dx.doi.org/10.3390/molecules26196076.

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Probiotics are beneficial active microorganisms that colonize the human intestines and change the composition of the flora in particular parts of the host. Recently, the use of probiotics to regulate intestinal flora to improve host immunity has received widespread attention. Recent evidence has shown that probiotics play significant roles in gut microbiota composition, which can inhibit the colonization of pathogenic bacteria in the intestine, help the host build a healthy intestinal mucosa protective layer, and enhance the host immune system. Based on the close relationship between the gut m

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29

Leonardi, Irina. "Beyond the gut." Science 377, no. 6602 (2022): 165. http://dx.doi.org/10.1126/science.abq6056.

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30

Clinton, Njinju Asaba, Sodiq Ayobami Hameed, Eugene Kusi Agyei, Joy Chinwendu Jacob, Victor Oyewale Oyebanji, and Cyril Ekabe Jabea. "Crosstalk between the Intestinal Virome and Other Components of the Microbiota, and Its Effect on Intestinal Mucosal Response and Diseases." Journal of Immunology Research 2022 (September 27, 2022): 1–23. http://dx.doi.org/10.1155/2022/7883945.

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In recent years, there has been ample evidence illustrating the effect of microbiota on gut immunity, homeostasis, and disease. Most of these studies have engaged more efforts in understanding the role of the bacteriome in gut mucosal immunity and disease. However, studies on the virome and its influence on gut mucosal immunity and pathology are still at infancy owing to limited metagenomic tools. Nonetheless, the existing studies on the virome have largely been focused on the bacteriophages as these represent the main component of the virome with little information on endogenous retroviruses

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31

Moeser, Adam J. "5 DPP Lecture: Investigating the Impact of Weaning and Biological Sex on Gut Development: Discovering New Targets for Gut Inflammation." Journal of Animal Science 101, Supplement_2 (2023): 62–63. http://dx.doi.org/10.1093/jas/skad341.069.

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Abstract Early life stress is known to have a profound impact on the development and function of the gut and immune system in various species, including pigs. In particular, the process of weaning is a significant source of stress in pigs and has been shown to negatively affect gut health and immunity. This presentation aims to examine the current knowledge on the impact of early life stress, particularly weaning, on gut development and immunity in pigs with a focus on chronic inflammation as a driver of disease risk. The presentation will also compare the immune system and gut development bet

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32

Obeagu, Emmanuel Ifeanyi, and Getrude Uzoma Obeagu. "Gut Mucosal Immunity in HIV-Exposed Infants: A Review." Asian Journal of Dental and Health Sciences 4, no. 2 (2024): 50–55. http://dx.doi.org/10.22270/ajdhs.v4i2.82.

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Gut mucosal immunity in infants exposed to Human Immunodeficiency Virus (HIV) presents a complex interplay of developmental processes, viral dynamics, and therapeutic interventions that significantly impact clinical outcomes. This review synthesizes current knowledge on the mechanisms, clinical implications, and therapeutic strategies concerning gut mucosal immunity in HIV-exposed infants. The gut mucosa serves as a critical site for immune maturation and defense against pathogens, but HIV infection disrupts this delicate balance, leading to compromised immune function and increased susceptibi

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33

Chandrasekaran, Preethi, Sabine Weiskirchen, and Ralf Weiskirchen. "Effects of Probiotics on Gut Microbiota: An Overview." International Journal of Molecular Sciences 25, no. 11 (2024): 6022. http://dx.doi.org/10.3390/ijms25116022.

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The role of probiotics in regulating intestinal flora to enhance host immunity has recently received widespread attention. Altering the human gut microbiota may increase the predisposition to several disease phenotypes such as gut inflammation and metabolic disorders. The intestinal microbiota converts dietary nutrients into metabolites that serve as biologically active molecules in modulating regulatory functions in the host. Probiotics, which are active microorganisms, play a versatile role in restoring the composition of the gut microbiota, helping to improve host immunity and prevent intes

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34

Li, Xin, Irina Leonardi, Alexa Semon, et al. "Sensing Fungal Dysbiosis by Gut-Resident CX3CR1+ Mononuclear Phagocytes Aggravates Allergic Airway Disease." Journal of Immunology 202, no. 1_Supplement (2019): 191.3. http://dx.doi.org/10.4049/jimmunol.202.supp.191.3.

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Abstract Sensing of the gut microbiota, including fungi, regulates mucosal immunity. Whether fungal sensing in the gut can influence immunity at other body sites is unknown. Here we show that fluconazole-induced gut fungal dysbiosis has persistent effects on allergic airway disease in a house dust mite challenge model. Mice with a defined community of bacteria, but lacking intestinal fungi were not susceptible to fluconazole-induced dysbiosis, while colonization with a fungal mixture recapitulated the detrimental effects. Gut-resident mononuclear phagocytes (MNPs) expressing the fractalkine re

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35

Pavia, Grazia, Nadia Marascio, Giovanni Matera, and Angela Quirino. "Does the Human Gut Virome Contribute to Host Health or Disease?" Viruses 15, no. 11 (2023): 2271. http://dx.doi.org/10.3390/v15112271.

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The human gastrointestinal (GI) tract harbors eukaryotic and prokaryotic viruses and their genomes, metabolites, and proteins, collectively known as the “gut virome”. This complex community of viruses colonizing the enteric mucosa is pivotal in regulating host immunity. The mechanisms involved in cross communication between mucosal immunity and the gut virome, as well as their relationship in health and disease, remain largely unknown. Herein, we review the literature on the human gut virome’s composition and evolution and the interplay between the gut virome and enteric mucosal immunity and t

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36

Wu, Xunyao, and Zhigang Tian. "Gut-liver axis: gut microbiota in shaping hepatic innate immunity." Science China Life Sciences 60, no. 11 (2017): 1191–96. http://dx.doi.org/10.1007/s11427-017-9128-3.

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37

Ngo, Vu L., Michal Kuczma, Estera Maxim, and Timothy L. Denning. "IL‐36 cytokines and gut immunity." Immunology 163, no. 2 (2021): 145–54. http://dx.doi.org/10.1111/imm.13310.

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38

Otto, Grant. "Gut mycobiota tunes humoral antifungal immunity." Nature Reviews Microbiology 19, no. 4 (2021): 222. http://dx.doi.org/10.1038/s41579-021-00529-4.

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39

Dillon, Stephanie M., and Cara C. Wilson. "Gut Innate Immunity and HIV Pathogenesis." Current HIV/AIDS Reports 18, no. 2 (2021): 128–38. http://dx.doi.org/10.1007/s11904-021-00544-3.

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40

Singh, Ankur. "Materials modulate immunity and gut microbiome." Nature Materials 19, no. 1 (2019): 3–4. http://dx.doi.org/10.1038/s41563-019-0557-3.

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41

Zhang, Husen, Joshua B. Sparks, Saikumar V. Karyala, Robert Settlage, and Xin M. Luo. "Host adaptive immunity alters gut microbiota." ISME Journal 9, no. 3 (2014): 770–81. http://dx.doi.org/10.1038/ismej.2014.165.

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42

Ghoddusi, H. B. "Gut Flora, Nutrition, Immunity and Health." International Journal of Dairy Technology 58, no. 4 (2005): 238. http://dx.doi.org/10.1111/j.1471-0307.2005.00184.x.

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43

Karagiannides, Iordanes, and Charalabos Pothoulakis. "Obesity, innate immunity and gut inflammation." Current Opinion in Gastroenterology 23, no. 6 (2007): 661–66. http://dx.doi.org/10.1097/mog.0b013e3282c8c8d3.

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44

Huang, Xiaojun, Shaoping Nie, and Mingyong Xie. "Interaction between gut immunity and polysaccharides." Critical Reviews in Food Science and Nutrition 57, no. 14 (2015): 2943–55. http://dx.doi.org/10.1080/10408398.2015.1079165.

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45

Messina, Valeria, Carla Buccione, Giulia Marotta, et al. "Gut Mesenchymal Stromal Cells in Immunity." Stem Cells International 2017 (2017): 1–6. http://dx.doi.org/10.1155/2017/8482326.

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Mesenchymal stromal cells (MSCs), first found in bone marrow (BM), are the structural architects of all organs, participating in most biological functions. MSCs possess tissue-specific signatures that allow their discrimination according to their origin and location. Among their multiple functions, MSCs closely interact with immune cells, orchestrating their activity to maintain overall homeostasis. The phenotype of tissue MSCs residing in the bowel overlaps with myofibroblasts, lining the bottom walls of intestinal crypts (pericryptal) or interspersed within intestinal submucosa (intercryptal

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46

Mueller, K. "Innate Immunity in the Fly Gut." Science Signaling 2, no. 80 (2009): ec243-ec243. http://dx.doi.org/10.1126/scisignal.280ec243.

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47

Dahele, Anna V., Marian C. Aldhous, Kathleen Kingstone, et al. "Gut mucosal immunity to tissue transglutaminase." Gastroenterology 118, no. 4 (2000): A365. http://dx.doi.org/10.1016/s0016-5085(00)83566-0.

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48

Valdés-Ramos, Roxana, Beatriz E. Martínez-Carrillo, Irma I. Aranda-González, et al. "Diet, exercise and gut mucosal immunity." Proceedings of the Nutrition Society 69, no. 4 (2010): 644–50. http://dx.doi.org/10.1017/s0029665110002533.

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Diet and exercise are primary strategies recommended for the control of the obesity epidemic. Considerable attention is being paid to the effect of both on the immune system. However, little research has been done on the effect of diet, nutrients or exercise on the mucosal immune system. The gastrointestinal tract (gut) is not only responsible for the entry of nutrients into the organism, but also for triggering the primary immune response to orally ingested antigens. The gut-associated lymphoid tissue contains a large amount of immune cells, disseminated all along the intestine in Peyer's pat

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49

Goldin, Barry R. "Gut Flora, Nutrition, Immunity and Health." American Journal of Clinical Nutrition 80, no. 2 (2004): 532. http://dx.doi.org/10.1093/ajcn/80.2.532.

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50

Scotti, Claudio. "GUT FLORA, NUTRITION, IMMUNITY AND HEALTH." Journal of Human Nutrition and Dietetics 17, no. 2 (2004): 159–60. http://dx.doi.org/10.1111/j.1365-277x.2004.00509.x.

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