How can probiotics and prebiotics impact mucosal immunity?

A core gut microbiome in obese and lean twins

Turnbaugh, P. J., Hamady, M., Yatsunenko, T., Cantarel, B. L., Duncan, A., Ley, R. E., Sogin, M. L., Jones, W. J., Roe, B. A., Affourtit, J. P., et al. (2009) · Nature · doi:10.1038/nature07540 · Cited by 7,823 · see citing works

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

Ogura, Y., Bonen, D. K., Inohara, N., Nicolae, D. L., Chen, F. F., Ramos, R., Britton, H., Moran, T., Karaliuskas, R., Duerr, R. H., et al. (2001) · Nature · doi:10.1038/35079114 · Cited by 5,030 · see citing works

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 · see citing works

<i>Faecalibacterium prausnitzii</i> is an anti-inflammatory commensal bacterium identified by gut microbiota analysis of Crohn disease patients

Sokol, H., Pigneur, B., Watterlot, L., Lakhdari, O., Bermúdez-Humarán, L. G., Gratadoux, J.-J., Blugeon, S., Bridonneau, C., Furet, J.-P., Corthier, G., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804812105 · Cited by 4,413 · see citing works

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

Rakoff-Nahoum, S., Paglino, J., Eslami-Varzaneh, F., Edberg, S., & Medzhitov, R. (2004) · Cell · doi:10.1016/j.cell.2004.07.002 · Cited by 4,251 · see citing works

Evolution of mammals and their gut microbes

Ley, R. E., Hamady, M., Lozupone, C., Turnbaugh, P. J., Ramey, R. R., Bircher, J. S., Schlegel, M. L., Tucker, T. A., Schrenzel, M. D., Knight, R., et al. (2008) · Science · doi:10.1126/science.1155725 · Cited by 3,747 · see citing works

Regulation of inflammatory responses by gut microbiota and chemoattractant receptor GPR43

Maslowski, K. M., Vieira, A. T., Ng, A., Kranich, J., Sierro, F., Yu, D., Schilter, H. C., Rolph, M. S., Mackay, F., Artis, D., et al. (2009) · Nature · doi:10.1038/nature08530 · Cited by 3,241 · see citing works

Changes in gut microbiota control inflammation in obese mice through a mechanism involving GLP-2-driven improvement of gut permeability

Cani, P. D., Possemiers, S., Van de Wiele, T., Guiot, Y., Everard, A., Rottier, O., Geurts, L., Naslain, D., Neyrinck, A., Lambert, D. M., et al. (2009) · Gut · doi:10.1136/gut.2008.165886 · Cited by 2,518 · see citing works

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 · see citing works

Guidelines for the evaluation of probiotics in food

Who, F. (2002) · Medical Entomology and Zoology · Cited by 1,843 · see citing works

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

Developmental microbial ecology of the neonatal gastrointestinal tract

Mackie, R. I., Sghir, A., & Gaskins, H. R. (1999) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/69.5.1035s · Cited by 1,360 · see citing works

Symbiotic gut microbes modulate human metabolic phenotypes

Li, M., Wang, B., Zhang, M., Rantalainen, M., Wang, S., Zhou, H., Zhang, Y., Shen, J., Pang, X., Zhang, M., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0712038105 · Cited by 1,144 · see citing works

Probiotic bacteria enhance murine and human intestinal epithelial barrier function

Madsen, K., Cornish, A. S., Soper, P., McKaigney, C. J., Jijon, H. B., Yachimec, C., Doyle, J. S. G., Jewell, L. D., & Simone, C. D. (2001) · Gastroenterology · doi:10.1053/gast.2001.27224 · Cited by 1,096 · see citing works

Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations

Hampe, J., Cuthbert, A. P., Croucher, P. J. P., Mirza, M. M., Mascheretti, S., Fisher, S. A., Frenzel, H., King, K., Hasselmeyer, A., Macpherson, A. J., et al. (2001) · The Lancet · doi:10.1016/s0140-6736(00)05063-7 · Cited by 1,090 · see citing works

Host interactions of probiotic bacterial surface molecules: comparison with commensals and pathogens

Lebeer, S., Vanderleyden, J., & De Keersmaecker, S. C. J. (2010) · Nature Reviews Microbiology · doi:10.1038/nrmicro2297 · Cited by 1,062 · see citing works

Towards the human intestinal microbiota phylogenetic core

Tap, J., Mondot, S., Levenez, F., Pelletier, E., Caron, C., Furet, J., Ugarte, E., Muñoz‐Tamayo, R., Paslier, D. L. E., Nalin, R., et al. (2009) · Environmental Microbiology · doi:10.1111/j.1462-2920.2009.01982.x · Cited by 927 · see citing works

Bacteriocin production as a mechanism for the antiinfective activity of <i>Lactobacillus salivarius</i> UCC118

Corr, S. C., Li, Y., Riedel, C. U., O'Toole, P. W., Hill, C., & Gahan, C. G. M. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0700440104 · Cited by 853 · see citing works

Soluble Proteins Produced by Probiotic Bacteria Regulate Intestinal Epithelial Cell Survival and Growth

Yan, F., Cao, H., Cover, T. L., Whitehead, R. H., Washington, M. K., & Polk, D. B. (2006) · Gastroenterology · doi:10.1053/j.gastro.2006.11.022 · Cited by 828 · see citing works

Live probiotics protect intestinal epithelial cells from the effects of infection with enteroinvasive <i>Escherichia coli</i> (EIEC)

Resta-Lenert, S., & Barrett, K. E. (2003) · Gut · doi:10.1136/gut.52.7.988 · Cited by 642 · see citing works

Single nucleotide polymorphisms of Toll-like receptors and susceptibility to infectious disease

Schröder, N. W. J., & Schumann, R. R. (2005) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(05)01308-3 · Cited by 638 · see citing works

Generation of regulatory dendritic cells and CD4 + Foxp3 + T cells by probiotics administration suppresses immune disorders

Kwon, H., Lee, C., So, J., Chae, C.-S., Hwang, J.-S., Sahoo, A., Nam, J. H., Rhee, J. H., Hwang, K.-C., & Im, S. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0904055107 · Cited by 627 · see citing works

Secreted bioactive factors from <i>Bifidobacterium infantis</i> enhance epithelial cell barrier function

Ewaschuk, J. B., Diaz, H., Meddings, L., Diederichs, B., Dmytrash, A., Backer, J., Looijer-van Langen, M., & Madsen, K. L. (2008) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.90227.2008 · Cited by 590 · see citing works

S layer protein A of Lactobacillus acidophilus NCFM regulates immature dendritic cell and T cell functions

Konstantinov, S. R., Smidt, H., de Vos, W. M., Bruijns, S. C. M., Singh, S., Valence, F., Mollé, D., Lortal, S., Altermann, E., Klaenhammer, T. R., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0810305105 · Cited by 568 · see citing works

Targeting the Human Microbiome With Antibiotics, Probiotics, and Prebiotics: Gastroenterology Enters the Metagenomics Era

Preidis, G. A., & Versalovic, J. A. (2009) · Gastroenterology · doi:10.1053/j.gastro.2009.01.072 · Cited by 485 · see citing works

Probiotic mixture VSL#3 protects the epithelial barrier by maintaining tight junction protein expression and preventing apoptosis in a murine model of colitis

Mennigen, R. B., Nolte, K., Rijcken, E. J. M., Utech, M., Loeffler, B., Senninger, N. J., & Bruewer, M. (2009) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.90534.2008 · Cited by 484 · see citing works

Clinical, microbiological, and immunological effects of fructo-oligosaccharide in patients with Crohn's disease

Lindsay, J. O. (2006) · Gut · doi:10.1136/gut.2005.074971 · Cited by 471 · see citing works

Role of fecal calprotectin as a biomarker of intestinal inflammation in inflammatory bowel disease

Konikoff, M. R., & Denson, L. A. (2006) · Inflammatory Bowel Diseases · doi:10.1097/00054725-200606000-00013 · Cited by 454 · see citing works

Enhanced antiinflammatory capacity of a Lactobacillus plantarum mutant synthesizing modified teichoic acids

Grangette, C., Nutten, S., Palumbo, E., Morath, S., Hermann, C., Dewulf, J., Pot, B., Härtung, T., Pascal Hols, A., & Mercenier, A. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504084102 · Cited by 443 · see citing works

Correlation between in vitro and in vivo immunomodulatory properties of lactic acid bacteria

Foligné, B. (2007) · World Journal of Gastroenterology · doi:10.3748/wjg.v13.i2.236 · Cited by 432 · see citing works

Molecular mechanisms underlying the probiotic effects of Escherichia coli Nissle 1917 involve ZO-2 and PKC? redistribution resulting in tight junction and epithelial barrier repair

Zyrek, A. A., Cichon, C., Helms, S., Enders, C., Sonnenborn, U., & Schmidt, M. A. (2006) · Cellular Microbiology · doi:10.1111/j.1462-5822.2006.00836.x · Cited by 427 · see citing works

Probiotic modulation of symbiotic gut microbial–host metabolic interactions in a humanized microbiome mouse model

Martin, F. J., Wang, Y., Sprenger, N., Yap, I. K. S., Lundstedt, T., Lek, P., Rezzi, S., Ramadan, Z., van Bladeren, P., Fay, L. B., et al. (2008) · Molecular Systems Biology · doi:10.1038/msb4100190 · Cited by 421 · see citing works

Probiotic Lactobacillus reuteri biofilms produce antimicrobial and anti-inflammatory factors

Jones, S. E., & Versalovic, J. A. (2009) · BMC Microbiology · doi:10.1186/1471-2180-9-35 · Cited by 417 · see citing works

Cell Surface-Associated Elongation Factor Tu Mediates the Attachment of <i>Lactobacillus johnsonii</i> NCC533 (La1) to Human Intestinal Cells and Mucins

Granato, D., Bergonzelli, G. E., Pridmore, R. D., Marvin, L., Rouvet, M., & Corthésy-Theulaz, I. E. (2004) · Infection and Immunity · doi:10.1128/iai.72.4.2160-2169.2004 · Cited by 410 · see citing works

Differential NF-κB pathways induction by Lactobacillus plantarum in the duodenum of healthy humans correlating with immune tolerance

van Baarlen, P., Troost, F. J., van Hemert, S., van Kraaij, C., de Vos, W. M., de Groot, P. J., Hooiveld, G. J. E. J., Brummer, R. J., & Kleerebezem, M. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0809919106 · Cited by 384 · see citing works

Improved immunogenicity of oral D x RRV reassortant rotavirus vaccine by Lactobacillus casei GG

Isolauri, E., Joensuu, J., Suomalainen, H., Luomala, M., & Vesikari, T. (1995) · Vaccine · doi:10.1016/0264-410x(95)93319-5 · Cited by 370 · see citing works

Care for the community

McFall‐Ngai, M. (2007) · Nature · doi:10.1038/445153a · Cited by 345 · see citing works

Prebiotics and Probiotics Science and Technology

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Induction of Human β-Defensin 2 by the ProbioticEscherichia coliNissle 1917 Is Mediated through Flagellin

Schlee, M., Wehkamp, J., Altenhoefer, A., Oelschlaeger, T. A., Stange, E. F., & Fellermann, K. (2007) · Infection and Immunity · doi:10.1128/iai.01563-06 · Cited by 315 · see citing works

GroEL of Lactobacillus johnsonii La1 (NCC 533) Is Cell Surface Associated: Potential Role in Interactions with the Host and the Gastric Pathogen Helicobacter pylori

Bergonzelli, G. E., Granato, D., Pridmore, R. D., Marvin, L., Donnicola, D., & Corthesy-Theulaz, I. E. (2005) · Infection and Immunity · doi:10.1128/iai.74.1.425-434.2006 · Cited by 302 · see citing works

Surface-layer protein extracts from Lactobacillus helveticus inhibit enterohaemorrhagic Escherichia coli O157:H7 adhesion to epithelial cells

Johnson-Henry, K. C., Hagen, K. E., Gordonpour, M., Tompkins, T. A., & Sherman, P. M. (2007) · Cellular Microbiology · doi:10.1111/j.1462-5822.2006.00791.x · Cited by 274 · see citing works

Inulin and Oligofructose: Review of Experimental Data on Immune Modulation

Seifert, S., & Watzl, B. (2007) · Journal of Nutrition · doi:10.1093/jn/137.11.2563s · Cited by 227 · see citing works

Oral supplementation with probiotics in very-low-birth-weight preterm infants: a randomized, double-blind, placebo-controlled trial

Rougé, C., Piloquet, H., Butel, M., Berger, B. W., Rochat, F., Ferraris, L., Robert, C. D., Legrand, A., de la Cochetière, M.-F., Nguyen, J., et al. (2009) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.2008.26919 · Cited by 216 · see citing works

The ability of fish oil to suppress tumor necrosis factor α production by peripheral blood mononuclear cells in healthy men is associated with polymorphisms in genes that influence tumor necrosis factor α production

Grimble, R. F., Howell, W. M., O’Reilly, G., Turner, S. J., Markovic, O., Hirrell, S., East, J. M., & Calder, P. C. (2002) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/76.2.454 · Cited by 212 · see citing works

Faecal SIgA secretion in infants fed on pre‐ or probiotic infant formula

Bakker‐Zierikzee, A. M., van Tol, E. A. F., Kroes, H., Alles, M., Kok, F. J., & BINDELS, J. G. (2006) · Pediatric Allergy and Immunology · doi:10.1111/j.1399-3038.2005.00370.x · Cited by 199 · see citing works

Probiotic bacteria stimulate virus-specific neutralizing antibodies following a booster polio vaccination

de Vrese, M., Rautenberg, P., Laue, C., Koopmans, M., Herremans, T., & Schrezenmeir, J. (2005) · European Journal of Nutrition · doi:10.1007/s00394-004-0541-8 · Cited by 190 · see citing works

Clinical trial: effect of active lactic acid bacteria on mucosal barrier function in patients with diarrhoea-predominant irritable bowel syndrome

ZENG, J., LI, Y. ‐., ZUO, X. ‐., ZHEN, Y. ‐., YANG, J., & LIU, C. ‐. (2008) · Alimentary Pharmacology &amp; Therapeutics · doi:10.1111/j.1365-2036.2008.03818.x · Cited by 189 · see citing works

Characterization of Inflammatory Bowel Disease With Urinary Metabolic Profiling

Williams, H. R. T., Cox, I. J., Walker, D. G., North, B. V., Patel, V. M., Marshall, S. E., Jewell, D. P., Ghosh, S. K., Thomas, H. J. W., TEARE, J. P., et al. (2009) · The American Journal of Gastroenterology · doi:10.1038/ajg.2009.175 · Cited by 183 · see citing works

Immunomodulatory Effects of Polysaccharides Produced by Lactobacillus delbrueckii ssp. bulgaricus OLL1073R-1

Makino, S., Ikegami, S., Kano, H., Sashihara, T., Sugano, H., Horiuchi, H., Saito, T. T., & Oda, M. (2006) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(06)72560-7 · Cited by 169 · see citing works

Effects of probiotic therapy in critically ill patients: a randomized, double-blind, placebo-controlled trial

Alberda, C., Gramlich, L. M., Meddings, J. B., Field, C. J., McCargar, L., Kutsogiannis, D. J., Fedorak, R. N., & Madsen, K. L. (2007) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/85.3.816 · Cited by 166 · see citing works

Effects of Bifidobacterium lactis Bb12 Supplementation on Body Weight, Fecal pH, Acetate, Lactate, Calprotectin, and IgA in Preterm Infants

Mohan, R., Koebnick, C., Schildt, J., Mueller, M., Radke, M., & Blaut, M. (2008) · Pediatric Research · doi:10.1203/pdr.0b013e318181b7fa · Cited by 165 · see citing works

Inflammatory bowel disease, gut bacteria and probiotic therapy

Reiff, C., & Kelly, D. (2009) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2009.08.004 · Cited by 164 · see citing works

ProbioticLactobacillusspp. DiminishHelicobacter hepaticus-Induced Inflammatory Bowel Disease in Interleukin-10-Deficient Mice

Peña, J. A., Rogers, A. B., Ge, Z., Ng, V., Li, S. Y., Fox, J. G., & Versalovic, J. A. (2005) · Infection and Immunity · doi:10.1128/iai.73.2.912-920.2005 · Cited by 160 · see citing works

C-reactive protein: How conformational changes influence inflammatory properties

Eisenhardt, S. U., Thiele, J. R., Bannasch, H., Stark, G. B., & Peter, K. (2009) · Cell Cycle · doi:10.4161/cc.8.23.10068 · Cited by 158 · see citing works

Modulation of colonic barrier function by the composition of the commensal flora in the rat

Garcia-Lafuente, A. M., Antolı́n, M., Guarner, F., Crespo, E., & Malagelada, J. R. (2001) · Gut · doi:10.1136/gut.48.4.503 · Cited by 156 · see citing works

COMPARISON OF CYTOKINE PRODUCTION IN CULTURES OF WHOLE HUMAN BLOOD AND PURIFIED MONONUCLEAR CELLS

Yaqoob, P., Newsholme, E. A., & Calder, P. C. (1999) · Cytokine · doi:10.1006/cyto.1998.0471 · Cited by 152 · see citing works

Suppressive Effect on Activation of Macrophages by Lactobacillus casei Strain Shirota Genes Determining the Synthesis of Cell Wall-Associated Polysaccharides

Yasuda, E., Serata, M., & Sako, T. (2008) · Applied and Environmental Microbiology · doi:10.1128/aem.00412-08 · Cited by 142 · see citing works

Functional Analysis of d -Alanylation of Lipoteichoic Acid in the Probiotic StrainLactobacillus rhamnosusGG

Vélez, M. P., Verhoeven, T. L. A., Draing, C., von Aulock, S., Pfitzenmaier, M., Geyer, A., Lambrichts, I., Grangette, C., Pot, B., Vanderleyden, J., et al. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.02083-06 · Cited by 125 · see citing works

Spatial and Temporal Expression of Lactobacillus plantarum Genes in the Gastrointestinal Tracts of Mice

Marco, M. L., Bongers, R. S., de Vos, W. M., & Kleerebezem, M. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.01475-06 · Cited by 117 · see citing works

Enhancement of gastric mucosal integrity by Lactobacillus rhamnosus GG

Lam, E. K. Y., Tai, E. K. K., Koo, M. W. L., Wong, H. P. S., Wu, W. K. K., Yu, L., So, W. H. L., Woo, P. C. Y., & Cho, C. H. (2007) · Life Sciences · doi:10.1016/j.lfs.2007.03.018 · Cited by 110 · see citing works

Lifestyle of Lactobacillus plantarum in the mouse caecum

Marco, M. L., Peters, T. H. F., Bongers, R. S., Douwe Molenaar, B., van Hemert, S., Sonnenburg, J. L., Gordon, J. I., & Kleerebezem, M. (2009) · Environmental Microbiology · doi:10.1111/j.1462-2920.2009.02001.x · Cited by 109 · see citing works

Gut health promoting activity of new putative probiotic/protective Lactobacillus spp. strains: A functional study in the small intestinal cell model

Nissen, L., Chingwaru, W., Sgorbati, B., Biavati, B., & Čenčič, A. (2009) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2009.08.027 · Cited by 95 · see citing works

Genotypic and Phenotypic Studies of Murine Intestinal Lactobacilli: Species Differences in Mice with and without Colitis

Peña, J. A., Li, S. Y., Wilson, P. H., Thibodeau, S. A., Szary, A. J., & Versalovic, J. A. (2004) · Applied and Environmental Microbiology · doi:10.1128/aem.70.1.558-568.2004 · Cited by 91 · see citing works

Identification of the transcriptional response of human intestinal mucosa to Lactobacillus plantarum WCFS1 in vivo

Troost, F. J., van Baarlen, P., Lindsey, P. J., Kodde, A., de Vos, W. M., Kleerebezem, M., & Brummer, R. J. (2008) · BMC Genomics · doi:10.1186/1471-2164-9-374 · Cited by 83 · see citing works

Symposium on ’Nutrition in the post-genomic era’ Plenary session 4: Genetic variation and diet-related disease

Howell, W. M., Calder, P. C., & Grimble, R. F. (2002) · Proceedings of The Nutrition Society · doi:10.1079/pns2002186 · Cited by 79 · see citing works

Effect of probiotic supplementation in the first 6 months of life on specific antibody responses to infant Hepatitis B vaccination

Soh, S. E., Ong, D. Q. R., Gerez, I., Zhang, X., Chollate, P., Shek, L. P.-C., Lee, B. W., & Aw, M. (2010) · Vaccine · doi:10.1016/j.vaccine.2010.01.020 · Cited by 78 · see citing works

Balancing inflammatory, lipid, and xenobiotic signaling pathways by VSL#3, a biotherapeutic agent, in the treatment of inflammatory bowel disease

Reiff, C., Delday, M. I., Rucklidge, G. J., Reid, M., Duncan, G., Wohlgemuth, S., Hörmannsperger, G., Loh, G., Blaut, M., Collie-Duguid, E. S. R., et al. (2009) · Inflammatory Bowel Diseases · doi:10.1002/ibd.20999 · Cited by 70 · see citing works

The role of NLRs and TLRs in the activation of the inflammasome

Netea, M. G., van de Veerdonk, F. L., Kullberg, B. J., van der Meer, J. W. M., & Joosten, L. A. B. (2008) · Expert Opinion on Biological Therapy · doi:10.1517/14712590802494212 · Cited by 65 · see citing works

Getting to the core of the gut microbiome

Tschöp, M. H., Hugenholtz, P., & Karp, C. L. (2009) · Nature Biotechnology · doi:10.1038/nbt0409-344 · Cited by 59 · see citing works

Elevated pro-inflammatory and lipotoxic mucosal lipidscharacterise irritable bowel syndrome

Kajander, K., Myllyluoma, E., Kyrönpalo, S., Rasmussen, M., Sipponen, P., Mattila, I. M., Seppänen‐Laakso, T., Vapaatalo, H., Orešič, M., & Korpela, R. (2009) · World Journal of Gastroenterology · doi:10.3748/wjg.15.6068 · Cited by 45 · see citing works

Mechanisms of Prebiotic Impact on Health

Steed, H., & Macfarlane, S. (2009) · Springer eBooks · doi:10.1007/978-0-387-79058-9_5 · Cited by 32 · see citing works

Vitamin‐regulated cytokines and growth factors in the CNS and elsewhere

Scalabrino, G. (2009) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2009.06417.x · Cited by 29 · see citing works

Emerging molecular insights into the interaction between probiotics and the host intestinal mucosa

Bron, P. A., van Baarlen, P., & Kleerebezem, M. (2012) · Nature Reviews Microbiology · doi:10.1038/nrmicro2690 · Cited by 690 · see citing works

Weaning stress and intestinal health of piglets: A review

Tang, X., Xiong, K., Fang, R., & Li, M. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1042778 · Cited by 415 · see citing works

Lactobacillus rhamnosus GG induces cGAS/STING- dependent type I interferon and improves response to immune checkpoint blockade

Si, W., Liang, H. L., Bugno, J., Xu, Q., Ding, X., Yang, K., Fu, Y., Weichselbaum, R. R., Zhao, X., & Wang, L. (2021) · Gut · doi:10.1136/gutjnl-2020-323426 · Cited by 327 · see citing works

Lactate and short chain fatty acids produced by microbial fermentation downregulate proinflammatory responses in intestinal epithelial cells and myeloid cells

Iraporda, C., Errea, A. J., Romanin, D., Cayet, D., Pereyra, E. N., Pignataro, O. P., Sirard, J., Garrote, G. L., Abraham, A. G., & Rumbo, M. (2015) · Immunobiology · doi:10.1016/j.imbio.2015.06.004 · Cited by 284 · see citing works

An anti-inflammatory diet as treatment for inflammatory bowel disease: a case series report

Olendzki, B. C., Silverstein, T., Persuitte, G. M., Ma, Y., Baldwin, K. R., & Cave, D. R. (2014) · Nutrition Journal · doi:10.1186/1475-2891-13-5 · Cited by 235 · see citing works

A Critical Look at Prebiotics Within the Dietary Fiber Concept

Verspreet, J., Damen, B., Broekaert, W. F., Verbeke, K., Delcour, J. A., & Courtin, C. M. (2016) · Annual Review of Food Science and Technology · doi:10.1146/annurev-food-081315-032749 · Cited by 186 · see citing works

Modulation of transcriptomic profile in aquatic animals: Probiotics, prebiotics and synbiotics scenarios

Dawood, M. A. O., Abo‐Al‐Ela, H. G., & Hasan, M. T. (2019) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2019.12.054 · Cited by 180 · see citing works

Enhancing the stress responses of probiotics for a lifestyle from gut to product and back again

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Impact of polydextrose on the faecal microbiota: a double-blind, crossover, placebo-controlled feeding study in healthy human subjects

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The Probiotic Mixture VSL#3 Has Differential Effects on Intestinal Immune Parameters in Healthy Female BALB/c and C57BL/6 Mice

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Current Concepts in Probiotic Safety and Efficacy

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Prebiotic Supplementation has Only Minimal Effects on Growth Efficiency, Intestinal Health and Disease Resistance of Westslope Cutthroat Trout Oncorhynchus clarkii lewisi Fed 30% Soybean Meal

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L. Plantarum and L. Lactis as a Promising Agent in Treatment of Inflammatory Bowel Disease and Colorectal Cancer

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Effect of Probiotics on Urinary Tract Infections in Children: A Systematic Review and Meta-Analysis

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Probiotics and Immune Response to Exercise

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CONSTRUCTION AND TESTING OF LIFE VACCINE BASED ON THE PROBIOTIC STRAIN ENTEROCOCCUS FAECIUM L3 AS MEANS FOR PREVENTION OF VAGINAL INFECTION CAUSED BY STREPTOCOCCUS AGALACTIAE

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The role of synbiotics in improving inflammatory status in nasopharyngeal carcinoma patients

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Vers une évaluation des potentialités probiotique et nutritionnelle des bactéries lactiques constitutives du microbiote d’un aliment fermenté traditionnel à base de mil par une approche moléculaire

Turpin, W. (2011) · theses.fr (ABES) · doi:10.70675/6fb75bf8zc7dcz44cfzaa0az934bb5f0d7f5 · Cited by 1 · see citing works

The influence of cell-free Lactobacillus rhamnosus GG conditioned medium on macrophage functional activity

Nanjundaiah, Y. S. (2016)

Efficacy of Symbiotics in an Experimental Model of Endotoxic Shock Induced by Lipopolysaccharide from Escherichia Coli

Ortíz, G. G. (2016) · International Journal of Food and Nutritional Science · doi:10.15436/2377-0619.16.865

Gastrointesnal Tract: Microflora and Transit Aspects

Silva, J. P. S. E., & Freitas, A. C. (2014) · doi:10.1201/b15676-5

Protective Effect of Homogeneous Polysaccharide from Wuguchong(HPW) on Intestinal Mucositis Induced by 5- Fluorouracil in MicePreprint

Shi, P., Zhao, T., Wang, W., Peng, F., Wang, T., Jia, Y., Zou, L., Wang, P., Yang, S., Fan, Y., et al. (2022) · Research Square · doi:10.21203/rs.3.rs-1194334/v1

Changes in lipid profiles of hypercholesterolemic rat (Rattus norvegicus) treated with iles-iles synbiotic effervescent tablets

Ngatirah, N., Wijaya, R. P., Ruswanto, A., Widyasaputra, R., & Syaflan, M. (2024) · IOP Conference Series Earth and Environmental Science · doi:10.1088/1755-1315/1377/1/012065

Additional file 1 of Effects of a complex probiotic preparation, Fengqiang Shengtai and coccidiosis vaccine on the performance and intestinal microbiota of broilers challenged with Eimeria spp.

Cai, H., Luo, S., Liu, Q., Zhou, Q., Yan, Z., Kang, Z., Liao, S., Li, J., Lv, M., Lin, X., et al. (2023) · Figshare · doi:10.6084/m9.figshare.23797410

Impact of Prebiotics, Probiotics and Gut Derived Metabolites on Host Immunity

Wu, R., Jeffrey, M. P., Johnson‐Henry, K. C., Green-Johnson, J. M., & Sherman, P. M. (2016) · LymphoSign Journal · doi:10.14785/lymphosign-2016-0012 · Cited by 20 · see citing works

Probiotics, Prebiotics and Immunomodulation of Gut Mucosal

Homeostasis, D., Hardy, H., Harris, J., Lyon, E., Beal, J., & Foey, A. (2013)

The impacts of probiotics and prebiotics on the gut mucosa and immune system through targeting inflammation and intestinal barrier function

Gorreja, F., Rush, S. T. A., Marques, T. M., Repsilber, D., Baker, A., Wall, R., & Brummer, R. J. (2018)

Modulation of Gut Microbiota and Immune System by Probiotics, Pre-biotics, and Post-biotics

Liu, Y., Wang, J., & Wu, C. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2021.634897 · Cited by 393 · see citing works

Probiotics, Prebiotics and Immunomodulation of Gut Mucosal Defences: Homeostasis and Immunopathology

Hardy, H., Harris, J., Lyon, E., Beal, J., & Foey, A. (2013) · Nutrients · doi:10.3390/nu5061869 · Cited by 551 · see citing works