On the public citation graph

Bile acid metabolites control Th17 and Treg cell differentiation

https://doi.org/10.1101/465344
0 signed · 133 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/0471142735.im0316bs113openalex-snapshot
Measuring Bioenergetics in T Cells Using a Seahorse Extracellular Flux Analyzer
inferredcites →https://doi.org/10.1002/dvg.22050openalex-snapshot
Mouse lines with photo‐activatable mitochondria to study mitochondrial dynamics
inferredcites →https://doi.org/10.1002/eji.201242740openalex-snapshot
Small molecule inhibitors of ROR γt: Targeting T h17 cells and other applications
inferredcites →https://doi.org/10.1007/978-1-4419-9034-1openalex-snapshot
Molecular Pathogenesis of Cholestasis
inferredcites →https://doi.org/10.1016/1074-7613(94)90045-0openalex-snapshot
Inhibition of Thl responses prevents inflammatory bowel disease in scid mice reconstituted with CD45RBhi CD4+ T cells
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.2012.05.031openalex-snapshot
Extrathymic Generation of Regulatory T Cells in Placental Mammals Mitigates Maternal-Fetal Conflict
inferredcites →https://doi.org/10.1016/j.cell.2014.07.031openalex-snapshot
Control of the Inheritance of Regulatory T Cell Identity by a cis Element in the Foxp3 Locus
inferredcites →https://doi.org/10.1016/j.cell.2016.05.035openalex-snapshot
Mitochondrial Dynamics Controls T Cell Fate through Metabolic Programming
inferredcites →https://doi.org/10.1016/j.cmet.2011.11.006openalex-snapshot
TGR5 Activation Inhibits Atherosclerosis by Reducing Macrophage Inflammation and Lipid Loading
inferredcites →https://doi.org/10.1016/j.cmet.2015.01.004openalex-snapshot
Identification of Natural RORγ Ligands that Regulate the Development of Lymphoid Cells
inferredcites →https://doi.org/10.1016/j.cmet.2016.12.018openalex-snapshot
Foxp3 Reprograms T Cell Metabolism to Function in Low-Glucose, High-Lactate Environments
inferredcites →https://doi.org/10.1016/j.immuni.2016.09.008openalex-snapshot
Bile Acids Control Inflammation and Metabolic Disorder through Inhibition of NLRP3 Inflammasome
inferredcites →https://doi.org/10.1016/j.immuni.2016.10.009openalex-snapshot
Bile Acids Control Inflammation and Metabolic Disorder through Inhibition of NLRP3 Inflammasome
inferredcites →https://doi.org/10.1016/j.immuni.2017.11.012openalex-snapshot
The Xenobiotic Transporter Mdr1 Enforces T Cell Homeostasis in the Presence of Intestinal Bile Acids
inferredcites →https://doi.org/10.1016/j.intimp.2012.11.017openalex-snapshot
Dose-dependent antiinflammatory effect of ursodeoxycholic acid in experimental colitis
inferredcites →https://doi.org/10.1016/j.it.2012.01.010openalex-snapshot
Metabolic pathways in T cell fate and function
inferredcites →https://doi.org/10.1016/j.molcel.2016.05.029openalex-snapshot
Interplay between Metabolism and Epigenetics: A Nuclear Adaptation to Environmental Changes
inferredcites →https://doi.org/10.1016/j.tiv.2012.12.020openalex-snapshot
Bile acids in the colon, from healthy to cytotoxic molecules
inferredcites →https://doi.org/10.1038/528s132aopenalex-snapshot
Q&A: Declan Murphy
inferredcites →https://doi.org/10.1038/nature08750openalex-snapshot
Role of conserved non-coding DNA elements in the Foxp3 gene in regulatory T-cell fate
inferredcites →https://doi.org/10.1038/nature09978openalex-snapshot
Digoxin and its derivatives suppress TH17 cell differentiation by antagonizing RORγt activity
inferredcites →https://doi.org/10.1038/nature10228openalex-snapshot
Control of TH17 cells occurs in the small intestine
inferredcites →https://doi.org/10.1038/nature10772openalex-snapshot
Extrathymically generated regulatory T cells control mucosal TH2 inflammation
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/nature13828openalex-snapshot
Precision microbiome reconstitution restores bile acid mediated resistance to Clostridium difficile
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/nature16141openalex-snapshot
A mechanism for expansion of regulatory T-cell repertoire and its role in self-tolerance
inferredcites →https://doi.org/10.1038/nature23475openalex-snapshot
Metabolic control of TH17 and induced Treg cell balance by an epigenetic mechanism
inferredcites →https://doi.org/10.1038/nchembio.1864openalex-snapshot
A biosynthetic pathway for a prominent class of microbiota-derived bile acids
inferredcites →https://doi.org/10.1038/nm.4375openalex-snapshot
D-mannose induces regulatory T cells and suppresses immunopathology
inferredcites →https://doi.org/10.1038/nrgastro.2013.151openalex-snapshot
Bile acid receptors as targets for drug development
inferredcites →https://doi.org/10.1056/nejm199810223391707openalex-snapshot
Molecular Pathogenesis of Cholestasis
inferredcites →https://doi.org/10.1073/pnas.1322807111openalex-snapshot
Oxysterols are agonist ligands of RORγt and drive Th17 cell differentiation
inferredcites →https://doi.org/10.1074/jbc.m114.621839openalex-snapshot
The Active Form of Vitamin D Transcriptionally Represses Smad7 Signaling and Activates Extracellular Signal-regulated Kinase (ERK) to Inhibit the Differentiation of a Inflammatory T Helper Cell Subset and Suppress Experimental Autoimmune Encephalomyelitis
inferredcites →https://doi.org/10.1084/jem.20112646openalex-snapshot
Smad3 binding to the foxp3 enhancer is dispensable for the development of regulatory T cells with the exception of the gut
inferredcites →https://doi.org/10.1084/jem.20151159openalex-snapshot
T cell metabolism drives immunity
inferredcites →https://doi.org/10.1084/jem.20171965openalex-snapshot
Bile acids in glucose metabolism in health and disease
inferredcites →https://doi.org/10.1111/j.1348-0421.1980.tb00578.xopenalex-snapshot
Intestinal Microflora and Bile Acids
inferredcites →https://doi.org/10.1126/science.1070477openalex-snapshot
Vitamin D Receptor As an Intestinal Bile Acid Sensor
inferredcites →https://doi.org/10.1126/science.aan5931openalex-snapshot
Gut microbiome–mediated bile acid metabolism regulates liver cancer via NKT cells
inferredcites →https://doi.org/10.1136/gutjnl-2012-302578openalex-snapshot
Connecting dysbiosis, bile-acid dysmetabolism and gut inflammation in inflammatory bowel diseases
inferredcites →https://doi.org/10.1152/ajpgi.00027.2007openalex-snapshot
Human cecal bile acids: concentration and spectrum
inferredcites →https://doi.org/10.1172/jci76012openalex-snapshot
Metabolic programming and PDHK1 control CD4+ T cell subsets and inflammation
inferredcites →https://doi.org/10.1194/jlr.d047506openalex-snapshot
A simple and accurate HPLC method for fecal bile acid profile in healthy and cirrhotic subjects: validation by GC-MS and LC-MS
inferredcites →https://doi.org/10.1194/jlr.r500013-jlr200openalex-snapshot
Bile salt biotransformations by human intestinal bacteria
inferredcites →https://doi.org/10.1210/me.2009-0507openalex-snapshot
Structural Basis for Hydroxycholesterols as Natural Ligands of Orphan Nuclear Receptor RORγ
inferredcites →https://doi.org/10.3748/wjg.15.3329openalex-snapshot
Bile acids as endogenous etiologic agents in gastrointestinal cancer
inferredcites →https://doi.org/10.4049/jimmunol.0803217openalex-snapshot
1,25-Dihydroxyvitamin D3 and IL-2 Combine to Inhibit T Cell Production of Inflammatory Cytokines and Promote Development of Regulatory T Cells Expressing CTLA-4 and FoxP3
inferredcites →https://doi.org/10.4049/jimmunol.0803978openalex-snapshot
The Bile Acid Receptor FXR Is a Modulator of Intestinal Innate Immunity
inferredcites →https://doi.org/10.4049/jimmunol.1101211openalex-snapshot
1,25-Dihyroxyvitamin D3 Promotes FOXP3 Expression via Binding to Vitamin D Response Elements in Its Conserved Noncoding Sequence Region
inferredcites →https://doi.org/10.4049/jimmunol.179.9.6273openalex-snapshot
Topically Applied 1,25-Dihydroxyvitamin D3 Enhances the Suppressive Activity of CD4+CD25+ Cells in the Draining Lymph Nodes

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1002/art.42635openalex-snapshot
Metabolomics and Machine Learning Identify Metabolic Differences and Potential Biomarkers for Frequent Versus Infrequent Gout Flares
inferred← citeshttps://doi.org/10.1002/cphy.c230012openalex-snapshot
Human Gut Microbiota in Cardiovascular Disease
inferred← citeshttps://doi.org/10.1002/eji.202249866openalex-snapshot
Emerging roles of host and microbial bioactive lipids in inflammatory bowel diseases
inferred← citeshttps://doi.org/10.1002/eji.202250002openalex-snapshot
Targeting regulatory T cell metabolism in disease: Novel therapeutic opportunities
inferred← citeshttps://doi.org/10.1002/eji.202250299openalex-snapshot
Bile acid‐activated receptors in innate and adaptive immunity: targeted drugs and biological agents
inferred← citeshttps://doi.org/10.1002/eji.202350460openalex-snapshot
TGF‐β1 signaling and Smad7 control T‐cell responses in health and immune‐mediated disorders
inferred← citeshttps://doi.org/10.1002/hep.31321openalex-snapshot
Inhibition of Sphingosine‐1‐Phosphate‐Induced Th17 Cells Ameliorates Alcohol‐Associated Steatohepatitis in Mice
inferred← citeshttps://doi.org/10.1002/jlb.1ma0122-513ropenalex-snapshot
Synthesis and identification of lithocholic acid 3-sulfate as RORγt ligand to inhibit Th17 cell differentiation
inferred← citeshttps://doi.org/10.1007/978-981-33-6785-2_10openalex-snapshot
Lipid Metabolism in Tumor-Infiltrating T Cells
inferred← citeshttps://doi.org/10.1007/978-981-99-9781-7_5openalex-snapshot
Regulatory T Cells for Control of Autoimmunity
inferred← citeshttps://doi.org/10.1007/s00011-023-01841-wopenalex-snapshot
Endoplasmic reticulum stress interferes with the development of type 1 regulating T cells
inferred← citeshttps://doi.org/10.1007/s00101-023-01258-4openalex-snapshot
Immunmodulation durch Ernährung bei kritisch kranken Patienten
inferred← citeshttps://doi.org/10.1007/s10620-022-07689-0openalex-snapshot
Role of Gut Microbiome in Immune Regulation and Immune Checkpoint Therapy of Colorectal Cancer
inferred← citeshttps://doi.org/10.1007/s11427-023-2353-0openalex-snapshot
Bile acid signaling in the regulation of whole body metabolic and immunological homeostasis
inferred← citeshttps://doi.org/10.1007/s11427-023-2595-5openalex-snapshot
Gut microbiota and healthy longevity
inferred← citeshttps://doi.org/10.1007/s12032-023-02289-yopenalex-snapshot
Evaluation of regulatory T-cells in cancer immunotherapy: therapeutic relevance of immune checkpoint inhibition
inferred← citeshttps://doi.org/10.1016/j.apsb.2021.07.022openalex-snapshot
Understanding the physiological functions of the host xenobiotic-sensing nuclear receptors PXR and CAR on the gut microbiome using genetically modified mice
inferred← citeshttps://doi.org/10.1016/j.jpba.2020.113660openalex-snapshot
Integrated metabolomics and network pharmacology approach to reveal immunomodulatory mechanisms of Yupingfeng granules
inferred← citeshttps://doi.org/10.1038/s12276-023-01042-9openalex-snapshot
Primary sclerosing cholangitis (PSC) and inflammatory bowel disease (IBD): a condition exemplifying the crosstalk of the gut–liver axis
inferred← citeshttps://doi.org/10.1038/s41385-020-00335-wopenalex-snapshot
Microbial modulation of intestinal T helper cell responses and implications for disease and therapy
inferred← citeshttps://doi.org/10.1038/s41385-020-00347-6openalex-snapshot
Bile acids modulate colonic MAdCAM-1 expression in a murine model of combined cholestasis and colitis
inferred← citeshttps://doi.org/10.1038/s41385-022-00547-2openalex-snapshot
Regulation of intestinal immunity by dietary fatty acids
inferred← citeshttps://doi.org/10.1038/s41390-025-03938-wopenalex-snapshot
Hirschsprung’s disease may increase the incidence of inflammatory bowel disease through alterations in CA1
inferred← citeshttps://doi.org/10.1038/s41423-021-00647-2openalex-snapshot
The microbiota is dispensable for the early stages of peripheral regulatory T cell induction within mesenteric lymph nodes
inferred← citeshttps://doi.org/10.1038/s41423-021-00753-1openalex-snapshot
Metabolic programming in dendritic cells tailors immune responses and homeostasis
inferred← citeshttps://doi.org/10.1038/s41429-024-00800-9openalex-snapshot
Therapeutic potential of isoallolithocholic acid in methicillin-resistant Staphylococcus Aureus peritoneal infection
inferred← citeshttps://doi.org/10.1038/s41467-020-20793-xopenalex-snapshot
Host immunity modulates the efficacy of microbiota transplantation for treatment of Clostridioides difficile infection
inferred← citeshttps://doi.org/10.1038/s41564-021-00948-2openalex-snapshot
Crosstalk between γδ T cells and the microbiota
inferred← citeshttps://doi.org/10.1038/s41564-023-01363-5openalex-snapshot
Microbiota-derived tryptophan catabolites mediate the chemopreventive effects of statins on colorectal cancer
inferred← citeshttps://doi.org/10.1038/s41564-023-01570-0openalex-snapshot
Gut commensal Christensenella minuta modulates host metabolism via acylated secondary bile acids
inferred← citeshttps://doi.org/10.1038/s41564-024-01617-wopenalex-snapshot
Altered microbial bile acid metabolism exacerbates T cell-driven inflammation during graft-versus-host disease
inferred← citeshttps://doi.org/10.1038/s41575-021-00566-7openalex-snapshot
Role of bile acids and their receptors in gastrointestinal and hepatic pathophysiology
inferred← citeshttps://doi.org/10.1038/s41579-022-00805-xopenalex-snapshot
Bile acids and the gut microbiota: metabolic interactions and impacts on disease
inferred← citeshttps://doi.org/10.1038/s41586-020-2396-4openalex-snapshot
A metabolic pathway for bile acid dehydroxylation by the gut microbiome
inferred← citeshttps://doi.org/10.1038/s41586-021-03832-5openalex-snapshot
Novel bile acid biosynthetic pathways are enriched in the microbiome of centenarians
inferred← citeshttps://doi.org/10.1096/fj.202200332ropenalex-snapshot
Bile acid restrained T cell activation explains cholestasis aggravated hepatitis B virus infection
inferred← citeshttps://doi.org/10.1097/hc9.0000000000000241openalex-snapshot
Recent updates on the role of the gut-liver axis in the pathogenesis of NAFLD/NASH, HCC, and beyond
inferred← citeshttps://doi.org/10.1097/hep.0000000000000506openalex-snapshot
Role of microbiome in autoimmune liver diseases
inferred← citeshttps://doi.org/10.1097/hep.0000000000001080openalex-snapshot
Immunobiology of primary sclerosing cholangitis
inferred← citeshttps://doi.org/10.1097/hep.0000000000001225openalex-snapshot
The immunological landscape of primary biliary cholangitis: Mechanisms and therapeutic prospects
inferred← citeshttps://doi.org/10.1097/hep.0000000000001236openalex-snapshot
PSC and colitis: A complex relationship
inferred← citeshttps://doi.org/10.1097/js9.0000000000001671openalex-snapshot
Establishment and validation of a predictive model of immune tolerance after pediatric liver transplantation: a multicenter cohort study
inferred← citeshttps://doi.org/10.1097/mco.0000000000000709openalex-snapshot
Emerging roles of bile acids in control of intestinal functions
inferred← citeshttps://doi.org/10.1097/mog.0000000000000820openalex-snapshot
Bile acids, bile pigments and colorectal cancer risk
inferred← citeshttps://doi.org/10.1097/mog.0000000000000997openalex-snapshot
Targeting bile salt homeostasis in biliary diseases
inferred← citeshttps://doi.org/10.1097/tp.0000000000005220openalex-snapshot
The Critical Role of Regulatory T Cells in Immune Tolerance and Rejection Following Liver Transplantation: Interactions With the Gut Microbiome
inferred← citeshttps://doi.org/10.1101/2024.03.20.584512openalex-snapshot
Gut microbiota gate host exposure to cholinesterase inhibitors from dietary Solanums
inferred← citeshttps://doi.org/10.1101/2025.08.17.670599openalex-snapshot
Crosstalk between CD8 + T cells and systemic bile acid metabolism controls LCMV-induced immunopathology
inferred← citeshttps://doi.org/10.1111/all.14223openalex-snapshot
T‐cell immunomodulation by bile acid metabolites
inferred← citeshttps://doi.org/10.1111/all.15006openalex-snapshot
Early intervention and prevention of allergic diseases
inferred← citeshttps://doi.org/10.1111/all.16684openalex-snapshot
Bifidobacterium breve M‐16V Alleviates Cow's Milk Allergy in a Mouse Model via Gut Microbiota‐Derived Indole‐3‐Propionic Acid‐Aryl Hydrocarbon Receptor Signaling Axis
inferred← citeshttps://doi.org/10.1111/apm.13401openalex-snapshot
Exploring the significance of microbiota metabolites in rheumatoid arthritis: uncovering their contribution from disease development to biomarker potential
inferred← citeshttps://doi.org/10.1111/exd.70108openalex-snapshot
The Role of Bile Acid in Immune‐Mediated Skin Diseases
inferred← citeshttps://doi.org/10.1111/imcb.12332openalex-snapshot
Bile acids mediate signaling between microbiome and the immune system
inferred← citeshttps://doi.org/10.1111/imm.13117openalex-snapshot
Intestinal epithelial cells: at the interface of the microbiota and mucosal immunity
inferred← citeshttps://doi.org/10.1111/imm.13672openalex-snapshot
Effect of gut flora mediated‐bile acid metabolism on intestinal immune microenvironment
inferred← citeshttps://doi.org/10.1111/liv.14906openalex-snapshot
A nonbile acid farnesoid X receptor agonist tropifexor potently inhibits cholestatic liver injury and fibrosis by modulating the gut–liver axis
inferred← citeshttps://doi.org/10.1111/pai.14003openalex-snapshot
The alternative bile acid pathway can predict food allergy persistence in early childhood
inferred← citeshttps://doi.org/10.1111/pai.70130openalex-snapshot
Environmental factors shaping atopic dermatitis: Lessons from longitudinal cohort studies
inferred← citeshttps://doi.org/10.1186/s13578-023-01109-0openalex-snapshot
Gut microbial metabolite deoxycholic acid facilitates Th17 differentiation through modulating cholesterol biosynthesis and participates in high-fat diet-associated colonic inflammation
inferred← citeshttps://doi.org/10.1186/s13578-023-01135-yopenalex-snapshot
The impact of the gut microbiome on tumor immunotherapy: from mechanism to application strategies
inferred← citeshttps://doi.org/10.1371/journal.ppat.1009891openalex-snapshot
Lung eosinophils elicited during allergic and acute aspergillosis express RORγt and IL-23R but do not require IL-23 for IL-17 production
inferred← citeshttps://doi.org/10.14309/ajg.0000000000000604openalex-snapshot
Targeting the Gut Microbiome as a Treatment for Primary Sclerosing Cholangitis: A Conceptional Framework
inferred← citeshttps://doi.org/10.18176/jiaci.0852openalex-snapshot
Microbiome and Allergy: New Insights and Perspectives
inferred← citeshttps://doi.org/10.20524/aog.2023.0834openalex-snapshot
An overview of recent treatment options for primary sclerosing cholangitis
inferred← citeshttps://doi.org/10.20892/j.issn.2095-3941.2023.0376openalex-snapshot
The role of intestinal flora on tumorigenesis, progression, and the efficacy of PD-1/PD-L1 antibodies in colorectal cancer
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1503415/v1openalex-snapshot
Dietary carbon loaded with nano-ZnO alters gut microbiota community to mediate bile acid metabolism and potentiate intestinal immune function of cattle
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1515102/v1openalex-snapshot
Ggraphene oxide loaded with nano-ZnO alters gut microbiota community to promote secondary bile acid synthesis and immunity response in fattening cattle
inferred← citeshttps://doi.org/10.22541/au.166899605.52123374/v1openalex-snapshot
Regulation of Immune Cell Functions by Bile Acid-Activated Receptors
inferred← citeshttps://doi.org/10.22541/au.170664260.07438524/v1openalex-snapshot
Potential mechanisms of action of the gut microbiota in antitumour immunity and immunotherapy
inferred← citeshttps://doi.org/10.3389/fendo.2025.1652731openalex-snapshot
Exercise reshapes gut microbiota to ameliorate core symptoms in PCOS: molecular mechanisms and therapeutic implications
inferred← citeshttps://doi.org/10.3389/fimmu.2021.711217openalex-snapshot
Gut-Liver Immune Traffic: Deciphering Immune-Pathogenesis to Underpin Translational Therapy
inferred← citeshttps://doi.org/10.3389/fmed.2026.1735850openalex-snapshot
The current consensus on ulcerative colitis, and the evidence and perspectives on the influence of gut microbiota on it
inferred← citeshttps://doi.org/10.3390/nu13051533openalex-snapshot
Diet–Microbiota Interactions in Inflammatory Bowel Disease
inferred← citeshttps://doi.org/10.3410/f.737934649.793578393openalex-snapshot
Faculty Opinions recommendation of An immunologic mode of multigenerational transmission governs a gut treg setpoint.
inferred← citeshttps://doi.org/10.3410/f.738152737.793576090openalex-snapshot
Faculty Opinions recommendation of A metabolic pathway for bile acid dehydroxylation by the gut microbiome.
inferred← citeshttps://doi.org/10.3410/f.738152737.793581741openalex-snapshot
Faculty Opinions recommendation of A metabolic pathway for bile acid dehydroxylation by the gut microbiome.
inferred← citeshttps://doi.org/10.59287/sbyc.588openalex-snapshot
Fekal Mikrobiota Transplantasyonu ve Veteriner Hekimlikte Kullanım Alanları
inferred← citeshttps://doi.org/10.7150/ijbs.53589openalex-snapshot
A perspective of intestinal immune-microbiome interactions in alcohol-associated Liver Disease
inferred← citeshttps://doi.org/10.7150/ijbs.71287openalex-snapshot
Lithocholic acid inhibits dendritic cell activation by reducing intracellular glutathione via TGR5 signaling
inferred← citeshttps://doi.org/10.7150/ijbs.79430openalex-snapshot
The role of gut microbiota in T cell immunity and immune mediated disorders
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.