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Adaptive immune education by gut microbiota antigens
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/jamapediatrics.2017.0378openalex-snapshot
Association Between Breast Milk Bacterial Communities and Establishment and Development of the Infant Gut Microbiome
inferredcites →https://doi.org/10.1002/art.40003openalex-snapshot
Evidence of the Immune Relevance of Prevotella copri, a Gut Microbe, in Patients With Rheumatoid Arthritis
inferredcites →https://doi.org/10.1002/eji.201546160openalex-snapshot
Commensal A4 bacteria inhibit intestinal Th2‐cell responses through induction of dendritic cell TGF‐β production
inferredcites →https://doi.org/10.1002/ibd.20237openalex-snapshot
Isolation of flagellated bacteria implicated in Crohnʼs disease
inferredcites →https://doi.org/10.1016/0140-6736(91)92104-aopenalex-snapshot
Reactivity of infiltrating T lymphocytes with microbial antigens in Crohn's disease
inferredcites →https://doi.org/10.1016/j.cell.2005.05.007openalex-snapshot
An Immunomodulatory Molecule of Symbiotic Bacteria Directs Maturation of the Host Immune System
inferredcites →https://doi.org/10.1016/j.cell.2007.08.017openalex-snapshot
Communicable Ulcerative Colitis Induced by T-bet Deficiency in the Innate Immune System
inferredcites →https://doi.org/10.1016/j.cell.2009.09.033openalex-snapshot
Induction of Intestinal Th17 Cells by Segmented Filamentous Bacteria
inferredcites →https://doi.org/10.1016/j.cell.2012.04.037openalex-snapshot
Gut Immune Maturation Depends on Colonization with a Host-Specific Microbiota
inferredcites →https://doi.org/10.1016/j.cell.2013.11.042openalex-snapshot
Sphingolipids from a Symbiotic Microbe Regulate Homeostasis of Host Intestinal Natural Killer T Cells
inferredcites →https://doi.org/10.1016/j.cell.2014.02.032openalex-snapshot
The Virome in Mammalian Physiology and Disease
inferredcites →https://doi.org/10.1016/j.cell.2014.08.006openalex-snapshot
Immunoglobulin A Coating Identifies Colitogenic Bacteria in Inflammatory Bowel Disease
inferredcites →https://doi.org/10.1016/j.cell.2015.08.058openalex-snapshot
Th17 Cell Induction by Adhesion of Microbes to Intestinal Epithelial Cells
inferredcites →https://doi.org/10.1016/j.cell.2015.08.061openalex-snapshot
An IL-23R/IL-22 Circuit Regulates Epithelial Serum Amyloid A to Promote Local Effector Th17 Responses
inferredcites →https://doi.org/10.1016/j.cell.2016.04.055openalex-snapshot
Maternal IgG and IgA Antibodies Dampen Mucosal T Helper Cell Responses in Early Life
inferredcites →https://doi.org/10.1016/j.celrep.2015.07.040openalex-snapshot
Intestinal Monocyte-Derived Macrophages Control Commensal-Specific Th17 Responses
inferredcites →https://doi.org/10.1016/j.celrep.2016.08.092openalex-snapshot
Rapid and Efficient Generation of Regulatory T Cells to Commensal Antigens in the Periphery
inferredcites →https://doi.org/10.1016/j.celrep.2017.02.061openalex-snapshot
T Follicular Helper Cells Promote a Beneficial Gut Ecosystem for Host Metabolic Homeostasis by Sensing Microbiota-Derived Extracellular ATP
inferredcites →https://doi.org/10.1016/j.chom.2007.09.013openalex-snapshot
IgA Response to Symbiotic Bacteria as a Mediator of Gut Homeostasis
inferredcites →https://doi.org/10.1016/j.chom.2008.09.009openalex-snapshot
Specific Microbiota Direct the Differentiation of IL-17-Producing T-Helper Cells in the Mucosa of the Small Intestine
inferredcites →https://doi.org/10.1016/j.chom.2009.06.005openalex-snapshot
Gut Commensal Bacteria Direct a Protective Immune Response against Toxoplasma gondii
inferredcites →https://doi.org/10.1016/j.chom.2011.08.005openalex-snapshot
The Genome of Th17 Cell-Inducing Segmented Filamentous Bacteria Reveals Extensive Auxotrophy and Adaptations to the Intestinal Environment
inferredcites →https://doi.org/10.1016/j.chom.2011.08.007openalex-snapshot
Complete Genome Sequences of Rat and Mouse Segmented Filamentous Bacteria, a Potent Inducer of Th17 Cell Differentiation
inferredcites →https://doi.org/10.1016/j.chom.2013.10.004openalex-snapshot
Intestinal Microbial Diversity during Early-Life Colonization Shapes Long-Term IgE Levels
inferredcites →https://doi.org/10.1016/j.chom.2014.02.005openalex-snapshot
The Treatment-Naive Microbiome in New-Onset Crohn’s Disease
inferredcites →https://doi.org/10.1016/j.chom.2014.12.009openalex-snapshot
MyD88 Signaling in T Cells Directs IgA-Mediated Control of the Microbiota to Promote Health
inferredcites →https://doi.org/10.1016/j.chom.2016.07.001openalex-snapshot
Gut Microbial Metabolites Fuel Host Antibody Responses
inferredcites →https://doi.org/10.1016/j.chom.2017.10.007openalex-snapshot
Segmented Filamentous Bacteria Provoke Lung Autoimmunity by Inducing Gut-Lung Axis Th17 Cells Expressing Dual TCRs
inferredcites →https://doi.org/10.1016/j.immuni.2008.05.014openalex-snapshot
Requirement for Lymphoid Tissue-Inducer Cells in Isolated Follicle Formation and T Cell-Independent Immunoglobulin A Generation in the Gut
inferredcites →https://doi.org/10.1016/j.immuni.2009.08.020openalex-snapshot
The Key Role of Segmented Filamentous Bacteria in the Coordinated Maturation of Gut Helper T Cell Responses
inferredcites →https://doi.org/10.1016/j.immuni.2010.06.001openalex-snapshot
Gut-Residing Segmented Filamentous Bacteria Drive Autoimmune Arthritis via T Helper 17 Cells
inferredcites →https://doi.org/10.1016/j.immuni.2011.03.029openalex-snapshot
A Requisite Role for Induced Regulatory T Cells in Tolerance Based on Expanding Antigen Receptor Diversity
inferredcites →https://doi.org/10.1016/j.immuni.2014.03.005openalex-snapshot
Segmented Filamentous Bacteria Antigens Presented by Intestinal Dendritic Cells Drive Mucosal Th17 Cell Differentiation
inferredcites →https://doi.org/10.1016/j.immuni.2014.03.009openalex-snapshot
Segmented Filamentous Bacterium Uses Secondary and Tertiary Lymphoid Tissues to Induce Gut IgA and Specific T Helper 17 Cell Responses
inferredcites →https://doi.org/10.1016/j.immuni.2014.05.016openalex-snapshot
Foxp3+ T Cells Regulate Immunoglobulin A Selection and Facilitate Diversification of Bacterial Species Responsible for Immune Homeostasis
inferredcites →https://doi.org/10.1016/j.immuni.2015.06.014openalex-snapshot
MyD88 Adaptor-Dependent Microbial Sensing by Regulatory T Cells Promotes Mucosal Tolerance and Enforces Commensalism
inferredcites →https://doi.org/10.1016/j.immuni.2015.08.007openalex-snapshot
Innate and Adaptive Humoral Responses Coat Distinct Commensal Bacteria with Immunoglobulin A
inferredcites →https://doi.org/10.1016/j.immuni.2015.08.011openalex-snapshot
BALB/c and C57BL/6 Mice Differ in Polyreactive IgA Abundance, which Impacts the Generation of Antigen-Specific IgA and Microbiota Diversity
inferredcites →https://doi.org/10.1016/j.immuni.2016.03.013openalex-snapshot
Gut Microbiota Drive Autoimmune Arthritis by Promoting Differentiation and Migration of Peyer’s Patch T Follicular Helper Cells
inferredcites →https://doi.org/10.1016/j.immuni.2017.06.013openalex-snapshot
Human Secretory IgM Emerges from Plasma Cells Clonally Related to Gut Memory B Cells and Targets Highly Diverse Commensals
inferredcites →https://doi.org/10.1016/j.jaci.2015.03.036openalex-snapshot
Human seroreactivity to gut microbiota antigens
inferredcites →https://doi.org/10.1016/s0091-6749(05)80067-3openalex-snapshot
A distinct subset of antineutrophil cytoplasmic antibodies is associated with inflammatory bowel disease
inferredcites →https://doi.org/10.1034/j.1600-065x.2001.1820115.xopenalex-snapshot
Control of intestinal inflammation by regulatory T cells
inferredcites →https://doi.org/10.1038/mi.2009.114openalex-snapshot
The development of intestinal lymphoid tissues at the interface of self and microbiota
inferredcites →https://doi.org/10.1038/mi.2010.29openalex-snapshot
A polysaccharide from the human commensal Bacteroides fragilis protects against CNS demyelinating disease
inferredcites →https://doi.org/10.1038/mi.2011.41openalex-snapshot
Secretory IgA's complex roles in immunity and mucosal homeostasis in the gut
inferredcites →https://doi.org/10.1038/nature06246openalex-snapshot
Recognition of microorganisms and activation of the immune response
inferredcites →https://doi.org/10.1038/nature08821openalex-snapshot
A human gut microbial gene catalogue established by metagenomic sequencing
inferredcites →https://doi.org/10.1038/nature10434openalex-snapshot
Peripheral education of the immune system by colonic commensal microbiota
inferredcites →https://doi.org/10.1038/nature10554openalex-snapshot
Commensal microbiota and myelin autoantigen cooperate to trigger autoimmune demyelination
inferredcites →https://doi.org/10.1038/nature10772openalex-snapshot
Extrathymically generated regulatory T cells control mucosal TH2 inflammation
inferredcites →https://doi.org/10.1038/nature11053openalex-snapshot
Human gut microbiome viewed across age and geography
inferredcites →https://doi.org/10.1038/nature11234openalex-snapshot
Structure, function and diversity of the healthy human microbiome
inferredcites →https://doi.org/10.1038/nature11550openalex-snapshot
Diversity, stability and resilience of the human gut microbiota
inferredcites →https://doi.org/10.1038/nature11551openalex-snapshot
Reciprocal interactions of the intestinal microbiota and immune system
inferredcites →https://doi.org/10.1038/nature12331openalex-snapshot
Treg induction by a rationally selected mixture of Clostridia strains from the human microbiota
inferredcites →https://doi.org/10.1038/nature12721openalex-snapshot
Commensal microbe-derived butyrate induces the differentiation of colonic regulatory T cells
inferredcites →https://doi.org/10.1038/nature12726openalex-snapshot
Metabolites produced by commensal bacteria promote peripheral regulatory T-cell generation
inferredcites →https://doi.org/10.1038/nature13279openalex-snapshot
Focused specificity of intestinal TH17 cells towards commensal bacterial antigens
inferredcites →https://doi.org/10.1038/nature13793openalex-snapshot
Artificial sweeteners induce glucose intolerance by altering the gut microbiota
inferredcites →https://doi.org/10.1038/nature14189openalex-snapshot
The biology of innate lymphoid cells
inferredcites →https://doi.org/10.1038/nature14452openalex-snapshot
Th17 cells transdifferentiate into regulatory T cells during resolution of inflammation
inferredcites →https://doi.org/10.1038/nature18847openalex-snapshot
The microbiome and innate immunity
inferredcites →https://doi.org/10.1038/nature22058openalex-snapshot
High-avidity IgA protects the intestine by enchaining growing bacteria
inferredcites →https://doi.org/10.1038/nbt.3353openalex-snapshot
A catalog of the mouse gut metagenome
inferredcites →https://doi.org/10.1038/ncomms8725openalex-snapshot
Active suppression of intestinal CD4+TCRαβ+ T-lymphocyte maturation during the postnatal period
inferredcites →https://doi.org/10.1038/ncomms9424openalex-snapshot
Antibiotics in neonatal life increase murine susceptibility to experimental psoriasis
inferredcites →https://doi.org/10.1038/ncomms9642openalex-snapshot
MHC variation sculpts individualized microbial communities that control susceptibility to enteric infection
inferredcites →https://doi.org/10.1038/ni.3213openalex-snapshot
Diversification of memory B cells drives the continuous adaptation of secretory antibodies to gut microbiota
inferredcites →https://doi.org/10.1038/nm.4039openalex-snapshot
Partial restoration of the microbiota of cesarean-born infants via vaginal microbial transfer
inferredcites →https://doi.org/10.1038/nm.4176openalex-snapshot
Neonatal gut microbiota associates with childhood multisensitized atopy and T cell differentiation
inferredcites →https://doi.org/10.1038/nri2527openalex-snapshot
Antiviral immune responses: triggers of or triggered by autoimmunity?
inferredcites →https://doi.org/10.1038/nri2832openalex-snapshot
New insights into the development of lymphoid tissues
inferredcites →https://doi.org/10.1038/nri2849openalex-snapshot
The importance of natural IgM: scavenger, protector and regulator
inferredcites →https://doi.org/10.1038/nri3667openalex-snapshot
Positive and negative selection of the T cell repertoire: what thymocytes see (and don't see)
inferredcites →https://doi.org/10.1038/nri3684openalex-snapshot
The mycobiota: interactions between commensal fungi and the host immune system
inferredcites →https://doi.org/10.1038/nrmicro3552openalex-snapshot
Gut biogeography of the bacterial microbiota
inferredcites →https://doi.org/10.1038/srep23129openalex-snapshot
Human gut colonisation may be initiated in utero by distinct microbial communities in the placenta and amniotic fluid
inferredcites →https://doi.org/10.1053/j.gastro.2016.05.050openalex-snapshot
Commensal-Specific CD4+ Cells From Patients With Crohn’s Disease Have a T-Helper 17 Inflammatory Profile
inferredcites →https://doi.org/10.1053/j.gastro.2017.07.047openalex-snapshot
Circulating and Tissue-Resident CD4+ T Cells With Reactivity to Intestinal Microbiota Are Abundant in Healthy Individuals and Function Is Altered During Inflammation
inferredcites →https://doi.org/10.1056/nejm199912303412707openalex-snapshot
Molecular Mimicry and Autoimmunity
inferredcites →https://doi.org/10.1056/nejmoa1205037openalex-snapshot
Duodenal Infusion of Donor Feces for Recurrent Clostridium difficile
inferredcites →https://doi.org/10.1073/pnas.0804812105openalex-snapshot
Faecalibacterium prausnitzii is an anti-inflammatory commensal bacterium identified by gut microbiota analysis of Crohn disease patients
inferredcites →https://doi.org/10.1073/pnas.0812681106openalex-snapshot
A dominant, coordinated T regulatory cell-IgA response to the intestinal microbiota
inferredcites →https://doi.org/10.1073/pnas.0909122107openalex-snapshot
Inducible Foxp3 + regulatory T-cell development by a commensal bacterium of the intestinal microbiota
inferredcites →https://doi.org/10.1073/pnas.0914121107openalex-snapshot
Secretory IgA-mediated protection against V. cholerae and heat-labile enterotoxin-producing enterotoxigenic Escherichia coli by rice-based vaccine
inferredcites →https://doi.org/10.1073/pnas.1000081107openalex-snapshot
Succession of microbial consortia in the developing infant gut microbiome
inferredcites →https://doi.org/10.1073/pnas.1000082107openalex-snapshot
Proinflammatory T-cell responses to gut microbiota promote experimental autoimmune encephalomyelitis
inferredcites →https://doi.org/10.1073/pnas.1002601107openalex-snapshot
Delivery mode shapes the acquisition and structure of the initial microbiota across multiple body habitats in newborns
inferredcites →https://doi.org/10.1073/pnas.1005963107openalex-snapshot
Impact of diet in shaping gut microbiota revealed by a comparative study in children from Europe and rural Africa
inferredcites →https://doi.org/10.1073/pnas.1315792111openalex-snapshot
Secretory antibodies in breast milk promote long-term intestinal homeostasis by regulating the gut microbiota and host gene expression
inferredcites →https://doi.org/10.1073/pnas.1412008111openalex-snapshot
Commensal bacteria protect against food allergen sensitization
inferredcites →https://doi.org/10.1073/pnas.1621258114openalex-snapshot
IgD class switching is initiated by microbiota and limited to mucosa-associated lymphoid tissue in mice
inferredcites →https://doi.org/10.1073/pnas.1711233114openalex-snapshot
Gut microbiota from multiple sclerosis patients enables spontaneous autoimmune encephalomyelitis in mice
inferredcites →https://doi.org/10.1073/pnas.91.1.163openalex-snapshot
Stimulation of transcytosis of the polymeric immunoglobulin receptor by dimeric IgA.
inferredcites →https://doi.org/10.1084/jem.190.7.915openalex-snapshot
Absence of Epithelial Immunoglobulin a Transport, with Increased Mucosal Leakiness, in Polymeric Immunoglobulin Receptor/Secretory Component–Deficient Mice
inferredcites →https://doi.org/10.1084/jem.20092253openalex-snapshot
Microbiota innate stimulation is a prerequisite for T cell spontaneous proliferation and induction of experimental colitis
inferredcites →https://doi.org/10.1084/jem.20111980openalex-snapshot
Age, microbiota, and T cells shape diverse individual IgA repertoires in the intestine
inferredcites →https://doi.org/10.1084/jem.20120822openalex-snapshot
Neuropilin-1 distinguishes natural and inducible regulatory T cells among regulatory T cell subsets in vivo
inferredcites →https://doi.org/10.1084/jem.20120914openalex-snapshot
Neuropilin 1 is expressed on thymus-derived natural regulatory T cells, but not mucosa-generated induced Foxp3+ T reg cells
inferredcites →https://doi.org/10.1111/imr.12066openalex-snapshot
CD 4 + T‐cell depletion in HIV infection: mechanisms of immunological failure
inferredcites →https://doi.org/10.1111/j.1462-2920.2012.02731.xopenalex-snapshot
‘ Candidatus Arthromitus’ revised: segmented filamentous bacteria in arthropod guts are members of Lachnospiraceae
inferredcites →https://doi.org/10.1126/science.1091334openalex-snapshot
Induction of Protective IgA by Intestinal Dendritic Cells Carrying Commensal Bacteria
inferredcites →https://doi.org/10.1126/science.1169152openalex-snapshot
Preferential Generation of Follicular B Helper T Cells from Foxp3 + T Cells in Gut Peyer's Patches
inferredcites →https://doi.org/10.1126/science.1188454openalex-snapshot
Reversible Microbial Colonization of Germ-Free Mice Reveals the Dynamics of IgA Immune Responses
inferredcites →https://doi.org/10.1126/science.1198469openalex-snapshot
Induction of Colonic Regulatory T Cells by Indigenous Clostridium Species
inferredcites →https://doi.org/10.1126/science.1208344openalex-snapshot
Linking Long-Term Dietary Patterns with Gut Microbial Enterotypes
inferredcites →https://doi.org/10.1126/science.1217718openalex-snapshot
The Inhibitory Receptor PD-1 Regulates IgA Selection and Bacterial Composition in the Gut
inferredcites →https://doi.org/10.1126/science.1219328openalex-snapshot
Microbial Exposure During Early Life Has Persistent Effects on Natural Killer T Cell Function
inferredcites →https://doi.org/10.1126/science.1220961openalex-snapshot
Acute Gastrointestinal Infection Induces Long-Lived Microbiota-Specific T Cell Responses
inferredcites →https://doi.org/10.1126/science.1241165openalex-snapshot
The Microbial Metabolites, Short-Chain Fatty Acids, Regulate Colonic T reg Cell Homeostasis
inferredcites →https://doi.org/10.1126/science.272.5258.54openalex-snapshot
Immunological Memory and Protective Immunity: Understanding Their Relation
inferredcites →https://doi.org/10.1126/science.288.5474.2222openalex-snapshot
A Primitive T Cell-Independent Mechanism of Intestinal Mucosal IgA Responses to Commensal Bacteria
inferredcites →https://doi.org/10.1126/science.8097338openalex-snapshot
Development of T H 1 CD4 + T Cells Through IL-12 Produced by Listeria -Induced Macrophages
inferredcites →https://doi.org/10.1126/science.aac4255openalex-snapshot
Commensal Bifidobacterium promotes antitumor immunity and facilitates anti–PD-L1 efficacy
inferredcites →https://doi.org/10.1126/science.aad1329openalex-snapshot
Anticancer immunotherapy by CTLA-4 blockade relies on the gut microbiota
inferredcites →https://doi.org/10.1126/science.aad9378openalex-snapshot
How colonization by microbiota in early life shapes the immune system
inferredcites →https://doi.org/10.1126/science.aad9948openalex-snapshot
Gene-microbiota interactions contribute to the pathogenesis of inflammatory bowel disease
inferredcites →https://doi.org/10.1126/science.aaf4822openalex-snapshot
IgA production requires B cell interaction with subepithelial dendritic cells in Peyer’s patches
inferredcites →https://doi.org/10.1126/science.aah5825openalex-snapshot
Lactobacillus reuteri induces gut intraepithelial CD4 + CD8αα + T cells
inferredcites →https://doi.org/10.1126/science.aan3706openalex-snapshot
Gut microbiome influences efficacy of PD-1–based immunotherapy against epithelial tumors
inferredcites →https://doi.org/10.1126/science.aan4236openalex-snapshot
Gut microbiome modulates response to anti–PD-1 immunotherapy in melanoma patients
inferredcites →https://doi.org/10.1126/science.aan4834openalex-snapshot
Seasonal cycling in the gut microbiome of the Hadza hunter-gatherers of Tanzania
inferredcites →https://doi.org/10.1126/science.aan6619openalex-snapshot
Natural polyreactive IgA antibodies coat the intestinal microbiota
inferredcites →https://doi.org/10.1126/sciimmunol.aal5068openalex-snapshot
Helicobacter species are potent drivers of colonic T cell responses in homeostasis and inflammation
inferredcites →https://doi.org/10.1126/sciimmunol.aao1314openalex-snapshot
Microbial antigen encounter during a preweaning interval is critical for tolerance to gut bacteria
inferredcites →https://doi.org/10.1126/scitranslmed.3008599openalex-snapshot
The Placenta Harbors a Unique Microbiome
inferredcites →https://doi.org/10.1126/scitranslmed.aaa4877openalex-snapshot
Functional characterization of IgA-targeted bacterial taxa from undernourished Malawian children that produce diet-dependent enteropathy
inferredcites →https://doi.org/10.1126/scitranslmed.aaf9655openalex-snapshot
IgA-coated E. coli enriched in Crohn’s disease spondyloarthritis promote T H 17-dependent inflammation
inferredcites →https://doi.org/10.1128/.67.4.1992-2000.1999openalex-snapshot
Segmented Filamentous Bacteria Are Potent Stimuli of a Physiologically Normal State of the Murine Gut Mucosal Immune System
inferredcites →https://doi.org/10.1128/iai.02856-14openalex-snapshot
Rapid Effects of a Protective O-Polysaccharide-Specific Monoclonal IgA on Vibrio cholerae Agglutination, Motility, and Surface Morphology
inferredcites →https://doi.org/10.1128/iai.63.8.3166-3173.1995openalex-snapshot
Selective neutralization of a bacterial enterotoxin by serum immunoglobulin A in response to mucosal disease
inferredcites →https://doi.org/10.1128/iai.68.10.5645-5651.2000openalex-snapshot
B-Cell Deficiency Predisposes Mice to Disseminating Anaerobic Infections: Protection by Passive Antibody Transfer
inferredcites →https://doi.org/10.1128/mbio.01346-15openalex-snapshot
Antibiotic-Driven Dysbiosis Mediates Intraluminal Agglutination and Alternative Segregation of Enterococcus faecium from the Intestinal Epithelium
inferredcites →https://doi.org/10.1136/gut.38.3.365openalex-snapshot
Mucosal antibodies in inflammatory bowel disease are directed against intestinal bacteria.
inferredcites →https://doi.org/10.1136/gutjnl-2011-301668openalex-snapshot
Secukinumab, a human anti-IL-17A monoclonal antibody, for moderate to severe Crohn's disease: unexpected results of a randomised, double-blind placebo-controlled trial
inferredcites →https://doi.org/10.1136/gutjnl-2012-303249openalex-snapshot
Decreased gut microbiota diversity, delayed Bacteroidetes colonisation and reduced Th1 responses in infants delivered by Caesarean section
inferredcites →https://doi.org/10.1136/gutjnl-2013-304833openalex-snapshot
A decrease of the butyrate-producing species Roseburia hominis and Faecalibacterium prausnitzii defines dysbiosis in patients with ulcerative colitis
inferredcites →https://doi.org/10.1146/annurev-micro-091313-103456openalex-snapshot
Effects of Antibiotics on Human Microbiota and Subsequent Disease
inferredcites →https://doi.org/10.1146/annurev.immunol.021908.132710openalex-snapshot
IL-17 and Th17 Cells
inferredcites →https://doi.org/10.1146/annurev.immunol.25.022106.141623openalex-snapshot
Regulatory T Cells: Mechanisms of Differentiation and Function
inferredcites →https://doi.org/10.1172/jci200420295openalex-snapshot
Bacterial flagellin is a dominant antigen in Crohn disease
inferredcites →https://doi.org/10.1186/s40168-016-0172-3openalex-snapshot
Comparison of placenta samples with contamination controls does not provide evidence for a distinct placenta microbiota
inferredcites →https://doi.org/10.1371/journal.pbio.1002533openalex-snapshot
Revised Estimates for the Number of Human and Bacteria Cells in the Body
inferredcites →https://doi.org/10.1542/peds.2005-2824openalex-snapshot
Factors Influencing the Composition of the Intestinal Microbiota in Early Infancy
inferredcites →https://doi.org/10.1542/peds.2010-2092openalex-snapshot
Prenatal or Early-Life Exposure to Antibiotics and Risk of Childhood Asthma: A Systematic Review
inferredcites →https://doi.org/10.1542/peds.72.3.317openalex-snapshot
Development and Differences of Intestinal Flora in the Neonatal Period in Breast-Fed and Bottle-Fed Infants
inferredcites →https://doi.org/10.3389/fimmu.2012.00051openalex-snapshot
Molecular Mechanisms of Treg-Mediated T Cell Suppression
inferredcites →https://doi.org/10.3389/fmicb.2017.00356openalex-snapshot
First Foods and Gut Microbes
inferredcites →https://doi.org/10.3389/fmicb.2017.01162openalex-snapshot
Geography, Ethnicity or Subsistence-Specific Variations in Human Microbiome Composition and Diversity
inferredcites →https://doi.org/10.4049/jimmunol.0904028openalex-snapshot
Expression of Helios, an Ikaros Transcription Factor Family Member, Differentiates Thymic-Derived from Peripherally Induced Foxp3+ T Regulatory Cells
inferredcites →https://doi.org/10.4049/jimmunol.1700171openalex-snapshot
Selective Induction of Homeostatic Th17 Cells in the Murine Intestine by Cholera Toxin Interacting with the Microbiota
inferredcites →https://doi.org/10.4049/jimmunol.172.10.5986openalex-snapshot
IL-10-Secreting Regulatory T Cells Do Not Express Foxp3 but Have Comparable Regulatory Function to Naturally Occurring CD4+CD25+ Regulatory T Cells
inferredcites →https://doi.org/10.4161/gmic.21008openalex-snapshot
Stabilization of the murine gut microbiome following weaning
inferredcites →https://doi.org/10.7554/elife.00458openalex-snapshot
Cohabiting family members share microbiota with one another and with their dogs
inferredcites →https://doi.org/10.7554/elife.01202openalex-snapshot
Expansion of intestinal Prevotella copri correlates with enhanced susceptibility to arthritis
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Subchronic exposure to environmentally relevant concentrations of di-(2-ethylhexyl) phthalate differentially affects the colon and ileum in adult female mice
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Conditioning of the immune system by the microbiome
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The gut ecosystem and immune tolerance
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Astragalus Polysaccharide improves immunogenicity of influenza vaccine as well as modulate gut microbiota in BALB/c mice
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The responses of the gut microbiota to MBL deficiency
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Gut dysbiosis, defective autophagy and altered immune responses in neurodegenerative diseases: Tales of a vicious cycle
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Impact of the microbiome on human, animal, and environmental health from a One Health perspective
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Friend or foe? Contextualizing Bacteroides through the lens of niche remodeling
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Dissect the mode of action of probiotics in affecting host-microbial interactions and immunity in food producing animals
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Age-related Eye Disease Studies Supplements and Genetic Risk Score Are Crucial Determinants of Intestinal Microbial Alterations in Advanced Age-Related Macular Degeneration
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Single-Cell RNA Sequencing Reveals Size-Dependent Effects of Polystyrene Microplastics on Immune and Secretory Cell Populations from Zebrafish Intestines
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Highly Branched RG-I Domain Enrichment Is Indispensable for Pectin Mitigating against High-Fat Diet-Induced Obesity
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Microbiota in health and diseases
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Human immunodeficiency virus-associated gut microbiome impacts systemic immunodeficiency and susceptibility to opportunistic gut infection
inferred← citeshttps://doi.org/10.1038/s41574-019-0254-yopenalex-snapshot
The heterogeneous pathogenesis of type 1 diabetes mellitus
inferred← citeshttps://doi.org/10.1038/s41584-021-00625-yopenalex-snapshot
Ankylosing spondylitis: an autoimmune or autoinflammatory disease?
inferred← citeshttps://doi.org/10.1038/s41591-023-02559-2openalex-snapshot
Dietary and commensal yeasts drive aberrant T cell responses in Crohn’s disease
inferred← citeshttps://doi.org/10.1038/s41598-020-71272-8openalex-snapshot
Abundance and nuclear antigen reactivity of intestinal and fecal Immunoglobulin A in lupus-prone mice at younger ages correlate with the onset of eventual systemic autoimmunity
inferred← citeshttps://doi.org/10.1038/s41598-021-93553-6openalex-snapshot
Attenuated asthma phenotype in mice with a fetal-like antigen receptor repertoire
inferred← citeshttps://doi.org/10.1038/s41598-023-35864-4openalex-snapshot
Development and verification of a combined diagnostic model for primary Sjögren's syndrome by integrated bioinformatics analysis and machine learning
inferred← citeshttps://doi.org/10.1038/s42003-023-04642-3openalex-snapshot
Optical imaging of the small intestine immune compartment across scales
inferred← citeshttps://doi.org/10.1039/c8cs00948aopenalex-snapshot
Molecular and cellular cues governing nanomaterial–mucosae interactions: from nanomedicine to nanotoxicology
inferred← citeshttps://doi.org/10.1079/hai.2023.0009openalex-snapshot
The Influence of Canine Ownership on Maternal and Fetal Microbiomes and Their Associated Health Outcomes: A Review of the Literature
inferred← citeshttps://doi.org/10.1080/1828051x.2024.2377642openalex-snapshot
Review: interactions between microplastics and the gastrointestinal microbiome
inferred← citeshttps://doi.org/10.1080/19490976.2020.1823801openalex-snapshot
Gut dysbiosis induced by cardiac pressure overload enhances adverse cardiac remodeling in a T cell-dependent manner
inferred← citeshttps://doi.org/10.1080/19490976.2022.2104086openalex-snapshot
Low abundance members of the gut microbiome exhibit high immunogenicity
inferred← citeshttps://doi.org/10.1080/19490976.2022.2117503openalex-snapshot
Preexisting antibodies targeting SARS-CoV-2 S2 cross-react with commensal gut bacteria and impact COVID-19 vaccine induced immunity
inferred← citeshttps://doi.org/10.1080/21505594.2026.2677297openalex-snapshot
Immune discrimination between commensals and pathogenic bacteria
inferred← citeshttps://doi.org/10.1093/ecco-jcc/jjae028openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/ibd/izac261openalex-snapshot
Epicutaneous Immunotherapy with CBir1 Alleviates Intestinal Inflammation
inferred← citeshttps://doi.org/10.1093/noajnl/vdab023openalex-snapshot
Human gut microbial communities dictate efficacy of anti-PD-1 therapy in a humanized microbiome mouse model of glioma
inferred← citeshttps://doi.org/10.1093/oxfordhb/9780190931544.013.17openalex-snapshot
Gut Barrier Permeability, Microbiota, and Brain Health
inferred← citeshttps://doi.org/10.1093/rheumatology/keaf360openalex-snapshot
Understanding the molecular basis of Sjögren’s disease using omic technologies
inferred← citeshttps://doi.org/10.1097/aci.0000000000000559openalex-snapshot
Role of the ocular surface microbiome in allergic disease
inferred← citeshttps://doi.org/10.1097/bor.0000000000000574openalex-snapshot
The microbiome in systemic autoimmune disease: mechanistic insights from recent studies
inferred← citeshttps://doi.org/10.1097/coh.0000000000000611openalex-snapshot
What is the collective effect of aging and HIV on the gut microbiome?
inferred← citeshttps://doi.org/10.1097/mcc.0000000000000800openalex-snapshot
The microbiome and the immune system in critical illness
inferred← citeshttps://doi.org/10.1097/md.0000000000039051openalex-snapshot
Gut microbiota and epigenetic choreography: Implications for human health: A review
inferred← citeshttps://doi.org/10.1101/2021.11.08.467805openalex-snapshot
Low Abundance Members of the Gut Microbiome are Potent Drivers of Immune Cell Education.
inferred← citeshttps://doi.org/10.1101/2023.11.15.23298517openalex-snapshot
Dynamic establishment and maintenance of the human intestinal B cell population and repertoire following transplantation
inferred← citeshttps://doi.org/10.1101/2024.05.20.594845openalex-snapshot
The ontogeny of immune tolerance: a model of early-life secretory IgA - gut microbiome interactions
inferred← citeshttps://doi.org/10.1111/1462-2920.14236openalex-snapshot
Environmental microbiology – the next 20 years: bioconnectivity and meta'omics 2.0
inferred← citeshttps://doi.org/10.1111/1753-0407.12915openalex-snapshot
Current understanding of the role of gut dysbiosis in type 1 diabetes
inferred← citeshttps://doi.org/10.1111/apm.70181openalex-snapshot
Detection of Fungal Translocation in Patients With Alcohol Use Disorder Using a Real‐Time PCR Assay
inferred← citeshttps://doi.org/10.1111/ejn.14610openalex-snapshot
Natural compulsive‐like behaviour in the deer mouse ( Peromyscus maniculatus bairdii ) is associated with altered gut microbiota composition
inferred← citeshttps://doi.org/10.1111/imcb.12393openalex-snapshot
A joint spotlight on research into the microbial immunity: beyond mere correlations
inferred← citeshttps://doi.org/10.1111/imm.12943openalex-snapshot
Neuroimmunology and neuroinflammation in autoimmune, neurodegenerative and psychiatric disease
inferred← citeshttps://doi.org/10.1111/imm.12975openalex-snapshot
Establishing the new playbook for interactions among microbiota, bacterial metabolites, adaptive immunity, autoimmune disease and metabolic syndrome
inferred← citeshttps://doi.org/10.1111/imm.13247openalex-snapshot
Immunological partners: the gut microbiome in homeostasis and disease
inferred← citeshttps://doi.org/10.1111/imm.13459openalex-snapshot
Preclinical stage abundance and nuclear antigen reactivity of faecal Immunoglobulin A vary among males and females of lupus‐prone mouse models
inferred← citeshttps://doi.org/10.1111/imr.12826openalex-snapshot
Microbial orchestra in juvenile idiopathic arthritis: Sounds of disarray?
inferred← citeshttps://doi.org/10.1111/mec.16491openalex-snapshot
Interaction between MHC diversity and constitution, gut microbiota and Astrovirus infections in a neotropical bat
inferred← citeshttps://doi.org/10.1111/pcmr.12957openalex-snapshot
Myron Gordon Award paper: Microbes, T‐cell diversity and pigmentation
inferred← citeshttps://doi.org/10.1126/scitranslmed.abq4006openalex-snapshot
Microbiome alteration via fecal microbiota transplantation is effective for refractory immune checkpoint inhibitor–induced colitis
inferred← citeshttps://doi.org/10.1128/iai.00502-24openalex-snapshot
Commensal resilience: ancient ecological lessons for the modern microbiota
inferred← citeshttps://doi.org/10.1128/mbio.00145-21openalex-snapshot
Immune Gene Expression Covaries with Gut Microbiome Composition in Stickleback
inferred← citeshttps://doi.org/10.1128/spectrum.00634-21openalex-snapshot
Lipidomics Analysis of Outer Membrane Vesicles and Elucidation of the Inositol Phosphoceramide Biosynthetic Pathway in Bacteroides thetaiotaomicron
inferred← citeshttps://doi.org/10.1155/2019/4735040openalex-snapshot
Gut Microbiota Modulation on Intestinal Mucosal Adaptive Immunity
inferred← citeshttps://doi.org/10.1155/mi/1951493openalex-snapshot
The Role of Inflammatory Cytokines in the Causal Pathway From Gut Microbiota to Sjögren’s Syndrome: Evidence From Mendelian Randomization
inferred← citeshttps://doi.org/10.1155/pedi/3013063openalex-snapshot
HLA‐C ∗ 0304 Associates With Beneficial Gut Microbiota and Later Onset of Type 1 Diabetes in Pediatric Cohorts
inferred← citeshttps://doi.org/10.1177/09612033231156075openalex-snapshot
Dietary patterns and life-styles of patients with gastrointestinal involvement of systemic lupus erythematosus: Questionnaire survey from a tertiary center of China
inferred← citeshttps://doi.org/10.1186/s12866-021-02312-0openalex-snapshot
Incongruence between dominant commensal donor microbes in recipient feces post fecal transplant and response to anti-PD-1 immunotherapy
inferred← citeshttps://doi.org/10.1186/s12979-021-00230-3openalex-snapshot
High-dimensional single cell mass cytometry analysis of the murine hematopoietic system reveals signatures induced by ageing and physiological pathogen challenges
inferred← citeshttps://doi.org/10.1186/s12979-021-00235-yopenalex-snapshot
Correction to: High-dimensional single cell mass cytometry analysis of the murine hematopoietic system reveals signatures induced by ageing and physiological pathogen challenges
inferred← citeshttps://doi.org/10.1186/s40560-025-00786-yopenalex-snapshot
Gut integrity in intensive care: alterations in host permeability and the microbiome as potential therapeutic targets
inferred← citeshttps://doi.org/10.1186/s42523-025-00440-wopenalex-snapshot
Fecal microbiota transplantation in pigs: current status and future perspective
inferred← citeshttps://doi.org/10.1371/journal.pbio.3003815openalex-snapshot
Immune surveillance and microbial escape in the aging host: Why does the microbiome lose its balance?
inferred← citeshttps://doi.org/10.1371/journal.pone.0226111openalex-snapshot
Sharing of gut microbial strains between selected individual sets of twins cohabitating for decades
inferred← citeshttps://doi.org/10.1371/journal.pone.0243176openalex-snapshot
Effect of IRT5 probiotics on dry eye in the experimental dry eye mouse model
inferred← citeshttps://doi.org/10.1371/journal.pone.0274633openalex-snapshot
Time series strain tracking analysis post fecal transplantation identifies individual specific patterns of fecal dominant donor, recipient, and unrelated microbial strains
inferred← citeshttps://doi.org/10.14201/gredos.153144openalex-snapshot
Análisis de los mecanismos moleculares de la predisposición genética a través del estudio de la leucemia infantil
inferred← citeshttps://doi.org/10.1530/rep-22-0303openalex-snapshot
Sex, puberty, and the gut microbiome
inferred← citeshttps://doi.org/10.17352/ojpch.000019openalex-snapshot
Developmental signifi cance of early gut-associated lymphoid tissue (GALT)- microbiota interactions in health and disease: Creating balance between tolerance and infl ammation in children
inferred← citeshttps://doi.org/10.17816/medjrf627266openalex-snapshot
Interrelation between gut microbiota and bronchial asthma
inferred← citeshttps://doi.org/10.18002/10612/13641openalex-snapshot
Modulación de la microbiota intestinal en el tratamiento de la enfermedad de hígado graso no alcohólico y síndrome metabólico. Estudio de un tratamiento experimental con quercetina y de la transferencia de microbiota a ratones libres de gérmenes = Intestinal microbiota modulation in the treatment…
inferred← citeshttps://doi.org/10.18174/502550openalex-snapshot
Gut microbiota and feather pecking : Integrating microbiota, behaviour, stress, serotonin and the immune system
inferred← citeshttps://doi.org/10.18297/etd/3966openalex-snapshot
Targeting pathological changes in the gut protects the CNS from neuropathology.
inferred← citeshttps://doi.org/10.18632/aging.102952openalex-snapshot
Dexmedetomidine alleviates sleep-restriction-mediated exaggeration of postoperative immunosuppression via splenic TFF2 in aged mice
inferred← citeshttps://doi.org/10.2147/jhc.s277870openalex-snapshot
Gut Microbiota, Peroxisome Proliferator-Activated Receptors, and Hepatocellular Carcinoma
inferred← citeshttps://doi.org/10.21608/ejabf.2020.93528openalex-snapshot
Immunogenization of Heat-Killed Vaccine Candidate from Aeromonas hydrophila in Catfish (Pangasius hypophthalamus) using Strain of Banjar, South Kalimantan, Indonesia
inferred← citeshttps://doi.org/10.21608/mid.2021.93318.1189openalex-snapshot
Update on the human microbiome and its clinical importance
inferred← citeshttps://doi.org/10.21638/spbu03.2025.203openalex-snapshot
“Enzymatic landscape” of the gut microbiome
inferred← citeshttps://doi.org/10.2174/1389450123666220418094853openalex-snapshot
Current Drug Targets for Gut Microbiota Biocorrection during the SARS-CoV-2 Pandemic: A Systematic Review
inferred← citeshttps://doi.org/10.2174/9789815324549125010014openalex-snapshot
Gut Microbiota and Future Research Directions
inferred← citeshttps://doi.org/10.2217/epi-2023-0382openalex-snapshot
Gut Microbiota and Epigenetics in Colorectal Cancer: Implications for Carcinogenesis and Therapeutic Intervention
inferred← citeshttps://doi.org/10.2337/db20-1177openalex-snapshot
Tolerogenic Dendritic Cells Shape a Transmissible Gut Microbiota That Protects From Metabolic Diseases
inferred← citeshttps://doi.org/10.24272/j.issn.2095-8137.2022.023openalex-snapshot
Maternal sleep deprivation induces gut microbial dysbiosis and neuroinflammation in offspring rats
inferred← citeshttps://doi.org/10.26442/20751753.2025.8.203344openalex-snapshot
The relationship between the composition of the gut microbiota and respiratory infection COVID-19: A review
inferred← citeshttps://doi.org/10.3168/jds.2020-19849openalex-snapshot
Comparison of isolation methods using commercially available kits for obtaining extracellular vesicles from cow milk
inferred← citeshttps://doi.org/10.32718/ujvas6-2.08openalex-snapshot
Comprehensive characteristics of rectal morphology in chickens with different types of autonomous regulation
inferred← citeshttps://doi.org/10.32718/ujvas9-2.04openalex-snapshot
Morphological characteristics of the rectum in chickens of different sexes
inferred← citeshttps://doi.org/10.33140/jeee.03.01.01openalex-snapshot
Integration of Antibody-Based and Electron-Based Diagnostics into Teledermatology for Skin Microbiome Monitoring
inferred← citeshttps://doi.org/10.3324/haematol.2020.247395openalex-snapshot
The clinical role of the gut microbiome and fecal microbiota transplantation in allogeneic stem cell transplantation
inferred← citeshttps://doi.org/10.3389/adar.2023.11092openalex-snapshot
Role of the gut-brain axis in HIV and drug abuse-mediated neuroinflammation
inferred← citeshttps://doi.org/10.3389/falgy.2026.1817101openalex-snapshot
Emerging molecular and environmental biomarkers of shrimp allergy in African Americans in the US
inferred← citeshttps://doi.org/10.3389/fcimb.2020.572912openalex-snapshot
Antibiotics as Major Disruptors of Gut Microbiota
inferred← citeshttps://doi.org/10.3389/fcimb.2021.752304openalex-snapshot
Microbial-Driven Immunological Memory and Its Potential Role in Microbiome Editing for the Prevention of Colorectal Cancer
inferred← citeshttps://doi.org/10.3389/fcimb.2021.755925openalex-snapshot
Porphyromonas gingivalis-Induced Cognitive Impairment Is Associated With Gut Dysbiosis, Neuroinflammation, and Glymphatic Dysfunction
inferred← citeshttps://doi.org/10.3389/fcimb.2022.852066openalex-snapshot
How Does Epstein–Barr Virus Interact With Other Microbiomes in EBV-Driven Cancers?
inferred← citeshttps://doi.org/10.3389/fcimb.2022.953718openalex-snapshot
The interplay between Helicobacter pylori and the gut microbiota: An emerging driver influencing the immune system homeostasis and gastric carcinogenesis
inferred← citeshttps://doi.org/10.3389/fcimb.2023.1102501openalex-snapshot
The gastrointestinal antibiotic resistome in pediatric leukemia and lymphoma patients
inferred← citeshttps://doi.org/10.3389/fcimb.2026.1905445openalex-snapshot
Gut-microbiota-mediated host immune modulation: mechanisms, pathological dysbiosis, and therapeutic frontiers
inferred← citeshttps://doi.org/10.3389/fimmu.2019.01551openalex-snapshot
The Commensal Microbiota and Viral Infection: A Comprehensive Review
inferred← citeshttps://doi.org/10.3389/fimmu.2019.02464openalex-snapshot
Influence of Gut Microbiota on Progression to Tuberculosis Generated by High Fat Diet-Induced Obesity in C3HeB/FeJ Mice
inferred← citeshttps://doi.org/10.3389/fimmu.2020.01755openalex-snapshot
Challenges for Clinical Development of Vaccines for Prevention of Hospital-Acquired Bacterial Infections
inferred← citeshttps://doi.org/10.3389/fimmu.2020.571731openalex-snapshot
Gut Microbiota as a Trigger for Metabolic Inflammation in Obesity and Type 2 Diabetes
inferred← citeshttps://doi.org/10.3389/fimmu.2020.599625openalex-snapshot
Host Defense Effectors Expressed by Hemocytes Shape the Bacterial Microbiota From the Scallop Hemolymph
inferred← citeshttps://doi.org/10.3389/fimmu.2020.608377openalex-snapshot
Immune Privilege: The Microbiome and Uveitis
inferred← citeshttps://doi.org/10.3389/fimmu.2020.612336openalex-snapshot
Gut Commensal-Induced IκBζ Expression in Dendritic Cells Influences the Th17 Response
inferred← citeshttps://doi.org/10.3389/fimmu.2021.662807openalex-snapshot
Exploring the Gut-Brain Axis for the Control of CNS Inflammatory Demyelination: Immunomodulation by Bacteroides fragilis’ Polysaccharide A
inferred← citeshttps://doi.org/10.3389/fimmu.2021.670500openalex-snapshot
Chronic Stress-Induced Depression and Anxiety Priming Modulated by Gut-Brain-Axis Immunity
inferred← citeshttps://doi.org/10.3389/fimmu.2022.1029948openalex-snapshot
The impact of aging on intestinal mucosal immune function and clinical applications
inferred← citeshttps://doi.org/10.3389/fimmu.2022.844335openalex-snapshot
Effects of Gut Microbiota on Host Adaptive Immunity Under Immune Homeostasis and Tumor Pathology State
inferred← citeshttps://doi.org/10.3389/fimmu.2023.1147447openalex-snapshot
Differential impact of environmental factors on systemic and localized autoimmunity
inferred← citeshttps://doi.org/10.3389/fimmu.2024.1323723openalex-snapshot
Gut microbiome, T cell subsets, and cytokine analysis identify differential biomarkers in tuberculosis
inferred← citeshttps://doi.org/10.3389/fimmu.2024.1365554openalex-snapshot
Emerging role of gut microbiota in autoimmune diseases
inferred← citeshttps://doi.org/10.3389/fimmu.2024.1375486openalex-snapshot
Dynamic establishment and maintenance of the human intestinal B cell population and repertoire following transplantation in a pediatric-dominated cohort
inferred← citeshttps://doi.org/10.3389/fimmu.2024.1429436openalex-snapshot
Microbiota activation and regulation of adaptive immunity
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1482033openalex-snapshot
Porphyromonas gingivalis: a potential trigger of neurodegenerative disease
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1532103openalex-snapshot
Effects of isolated, confined and extreme environments on parameters of the immune system - a systematic review
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1584001openalex-snapshot
Interacting roles of gut microbiota and T cells in the development of autoimmune hepatitis
inferred← citeshttps://doi.org/10.3389/fimmu.2026.1884535openalex-snapshot
Gut microbiota dysbiosis in rheumatoid arthritis: mechanisms linking intestinal barrier dysfunction to synovial inflammation
inferred← citeshttps://doi.org/10.3389/fmed.2022.915179openalex-snapshot
Gut Microbiota in Systemic Lupus Erythematosus and Correlation With Diet and Clinical Manifestations
inferred← citeshttps://doi.org/10.3389/fmicb.2018.01394openalex-snapshot
Beyond Bacteria: Bacteriophage-Eukaryotic Host Interactions Reveal Emerging Paradigms of Health and Disease
inferred← citeshttps://doi.org/10.3389/fmicb.2021.709562openalex-snapshot
Circulating Antibodies to Skin Bacteria Detected by Serological Lateral Flow Immunoassays Differentially Correlated With Bacterial Abundance
inferred← citeshttps://doi.org/10.3389/fmicb.2021.772863openalex-snapshot
The Gut Microbiota of Newborn Calves and Influence of Potential Probiotics on Reducing Diarrheic Disease by Inhibition of Pathogen Colonization
inferred← citeshttps://doi.org/10.3389/fmicb.2022.1034537openalex-snapshot
Immune mechanism of gut microbiota and its metabolites in the occurrence and development of cardiovascular diseases
inferred← citeshttps://doi.org/10.3389/fmicb.2022.958739openalex-snapshot
Mucosal immune cell populations and the bacteriome of adenoids and tonsils from people living with HIV on suppressive antiretroviral therapy
inferred← citeshttps://doi.org/10.3389/fmicb.2022.996031openalex-snapshot
Intestinal microbiome–rheumatoid arthritis crosstalk: The therapeutic role of probiotics
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1098386openalex-snapshot
Role of gut microbiota in infectious and inflammatory diseases
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1118529openalex-snapshot
Communication of gut microbiota and brain via immune and neuroendocrine signaling
inferred← citeshttps://doi.org/10.3389/fmicb.2026.1901528openalex-snapshot
Tirzepatide and the gut microbiota–obesity axis: metabolic mechanisms and therapeutic perspectives
inferred← citeshttps://doi.org/10.3389/fnins.2026.1952549openalex-snapshot
Loss of microbial diversity from human–microbe coevolution: immune, epigenetic, and enteric nervous system mechanisms linking dysbiosis to neuropsychiatric and neurodegenerative diseases
inferred← citeshttps://doi.org/10.3389/fnut.2020.606171openalex-snapshot
Can the FUT2 Non-secretor Phenotype Associated With Gut Microbiota Increase the Children Susceptibility for Type 1 Diabetes? A Mini Review
inferred← citeshttps://doi.org/10.3389/fnut.2021.644138openalex-snapshot
Factors Affecting Gut Microbiome in Daily Diet
inferred← citeshttps://doi.org/10.3389/fnut.2022.1050099openalex-snapshot
Mushrooms as future generation healthy foods
inferred← citeshttps://doi.org/10.3389/fnut.2025.1694093openalex-snapshot
Changes in and relationships between human milk oligosaccharides and microRNAs in milk-derived extracellular vesicles during the first 4 months of lactation
inferred← citeshttps://doi.org/10.3389/fonc.2023.1344328openalex-snapshot
The role of microbiomes in gastrointestinal cancers: new insights
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