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NKT cells and the regulation of intestinal immunity: a two‐way street

https://doi.org/10.1111/febs.15238
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What this work says

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

inferredcites →https://doi.org/10.1002/eji.200526157openalex-snapshot
Cell wall glycosphingolipids ofSphingomonas paucimobilisare CD1d-specific ligands for NKT cells
inferredcites →https://doi.org/10.1007/978-3-662-43492-5_10openalex-snapshot
Role of IL-22 in Microbial Host Defense
inferredcites →https://doi.org/10.1007/s00535-012-0591-2openalex-snapshot
Blocking IL-25 signalling protects against gut inflammation in a type-2 model of colitis by suppressing nuocyte and NKT derived IL-13
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.2014.03.011openalex-snapshot
Role of the Microbiota in Immunity and Inflammation
inferredcites →https://doi.org/10.1016/j.cell.2016.02.048openalex-snapshot
Hallmarks of Tissue-Resident Lymphocytes
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.cell.2017.11.036openalex-snapshot
Initiation of Antiviral B Cell Immunity Relies on Innate Signals from Spatially Positioned NKT Cells
inferredcites →https://doi.org/10.1016/j.cell.2018.04.037openalex-snapshot
Dietary and Microbial Oxazoles Induce Intestinal Inflammation by Modulating Aryl Hydrocarbon Receptor Responses
inferredcites →https://doi.org/10.1016/j.coi.2013.01.002openalex-snapshot
Natural Killer T cell obsession with self-antigens
inferredcites →https://doi.org/10.1016/j.coi.2017.07.013openalex-snapshot
Four pathways of CD1 antigen presentation to T cells
inferredcites →https://doi.org/10.1016/j.coi.2018.01.006openalex-snapshot
Transcriptional and epigenetic regulation of innate-like T lymphocyte development
inferredcites →https://doi.org/10.1016/j.gastro.2005.05.002openalex-snapshot
Interleukin-13 Is the Key Effector Th2 Cytokine in Ulcerative Colitis That Affects Epithelial Tight Junctions, Apoptosis, and Cell Restitution
inferredcites →https://doi.org/10.1016/j.immuni.2007.08.017openalex-snapshot
Activation of Invariant NKT Cells by Toll-like Receptor 9-Stimulated Dendritic Cells Requires Type I Interferon and Charged Glycosphingolipids
inferredcites →https://doi.org/10.1016/j.immuni.2008.05.001openalex-snapshot
The Biology of Intestinal Immunoglobulin A Responses
inferredcites →https://doi.org/10.1016/j.immuni.2009.05.010openalex-snapshot
T Cell Receptor CDR2β and CDR3β Loops Collaborate Functionally to Shape the iNKT Cell Repertoire
inferredcites →https://doi.org/10.1016/j.immuni.2009.08.011openalex-snapshot
Regulatory T Cells Reinforce Intestinal Homeostasis
inferredcites →https://doi.org/10.1016/j.immuni.2010.08.003openalex-snapshot
Lysosomal α-Galactosidase Controls the Generation of Self Lipid Antigens for Natural Killer T Cells
inferredcites →https://doi.org/10.1016/j.immuni.2015.06.025openalex-snapshot
Tissue-Specific Distribution of iNKT Cells Impacts Their Cytokine Response
inferredcites →https://doi.org/10.1016/s1074-7613(02)00453-3openalex-snapshot
Oxazolone Colitis, a Th2 Colitis Model Resembling Ulcerative Colitis, Is Mediated by IL-13-Producing NK-T Cells
inferredcites →https://doi.org/10.1038/mi.2008.46openalex-snapshot
Epithelial apoptosis is a prominent feature of the epithelial barrier disturbance in intestinal inflammation: effect of pro-inflammatory interleukin-13 on epithelial cell function
inferredcites →https://doi.org/10.1038/mi.2012.77openalex-snapshot
IL-9-producing invariant NKT cells protect against DSS-induced colitis in an IL-4-dependent manner
inferredcites →https://doi.org/10.1038/mi.2014.13openalex-snapshot
Invariant natural killer T cells developing in the human fetus accumulate and mature in the small intestine
inferredcites →https://doi.org/10.1038/mi.2015.78openalex-snapshot
Cytokine expression by invariant natural killer T cells is tightly regulated throughout development and settings of type-2 inflammation
inferredcites →https://doi.org/10.1038/mi.2017.34openalex-snapshot
Unique invariant natural killer T cells promote intestinal polyps by suppressing TH1 immunity and promoting regulatory T cells
inferredcites →https://doi.org/10.1038/nature03407openalex-snapshot
Recognition of bacterial glycosphingolipids by natural killer T cells
inferredcites →https://doi.org/10.1038/nature03408openalex-snapshot
Exogenous and endogenous glycolipid antigens activate NKT cells during microbial infections
inferredcites →https://doi.org/10.1038/nature06005openalex-snapshot
Unravelling the pathogenesis of inflammatory bowel disease
inferredcites →https://doi.org/10.1038/nature12240openalex-snapshot
Innate lymphoid cells regulate CD4+ T-cell responses to intestinal commensal bacteria
inferredcites →https://doi.org/10.1038/nature13150openalex-snapshot
Protective mucosal immunity mediated by epithelial CD1d and IL-10
inferredcites →https://doi.org/10.1038/ni.2166openalex-snapshot
Identification of Bcl-6-dependent follicular helper NKT cells that provide cognate help for B cell responses
inferredcites →https://doi.org/10.1038/ni.2172openalex-snapshot
Invariant natural killer T cells direct B cell responses to cognate lipid antigen in an IL-21-dependent manner
inferredcites →https://doi.org/10.1038/ni.2731openalex-snapshot
Steady-state production of IL-4 modulates immunity in mouse strains and is determined by lineage diversity of iNKT cells
inferredcites →https://doi.org/10.1038/ni.3047openalex-snapshot
Regulatory iNKT cells lack expression of the transcription factor PLZF and control the homeostasis of Treg cells and macrophages in adipose tissue
inferredcites →https://doi.org/10.1038/ni.3298openalex-snapshot
The burgeoning family of unconventional T cells
inferredcites →https://doi.org/10.1038/ni.3437openalex-snapshot
Innate-like functions of natural killer T cell subsets result from highly divergent gene programs
inferredcites →https://doi.org/10.1038/ni1380openalex-snapshot
Natural killer T cells recognize diacylglycerol antigens from pathogenic bacteria
inferredcites →https://doi.org/10.1038/nm.3321openalex-snapshot
Invariant natural killer T cells recognize a fungal glycosphingolipid that can induce airway hyperreactivity
inferredcites →https://doi.org/10.1038/nri1309openalex-snapshot
NKT cells: what's in a name?
inferredcites →https://doi.org/10.1038/nri3369openalex-snapshot
Invariant natural killer T cells: an innate activation scheme linked to diverse effector functions
inferredcites →https://doi.org/10.1038/s41467-018-05026-6openalex-snapshot
TCR signal strength controls thymic differentiation of iNKT cell subsets
inferredcites →https://doi.org/10.1038/s41467-018-05095-7openalex-snapshot
Altered thymic differentiation and modulation of arthritis by invariant NKT cells expressing mutant ZAP70
inferredcites →https://doi.org/10.1038/s41577-018-0034-2openalex-snapshot
Tissue-specific functions of invariant natural killer T cells
inferredcites →https://doi.org/10.1053/gast.2000.9114openalex-snapshot
Activation of natural killer T cells by α-galactosylceramide in the presence of CD1d provides protection against colitis in mice
inferredcites →https://doi.org/10.1053/j.gastro.2011.10.030openalex-snapshot
Dysregulation of CD1d-Restricted Type II Natural Killer T Cells Leads to Spontaneous Development of Colitis in Mice
inferredcites →https://doi.org/10.1053/j.gastro.2012.04.017openalex-snapshot
Intestinal Microbes Affect Phenotypes and Functions of Invariant Natural Killer T Cells in Mice
inferredcites →https://doi.org/10.1073/pnas.0611139104openalex-snapshot
Normal development and function of invariant natural killer T cells in mice with isoglobotrihexosylceramide (iGb3) deficiency
inferredcites →https://doi.org/10.1073/pnas.0801375105openalex-snapshot
NK T cells provide lipid antigen-specific cognate help for B cells
inferredcites →https://doi.org/10.1073/pnas.0802968105openalex-snapshot
B cell receptor-mediated uptake of CD1d-restricted antigen augments antibody responses by recruiting invariant NKT cell help in vivo
inferredcites →https://doi.org/10.1073/pnas.1521846113openalex-snapshot
Transcription factor Bcl11b sustains iNKT1 and iNKT2 cell programs, restricts iNKT17 cell program, and governs iNKT cell survival
inferredcites →https://doi.org/10.1084/jem.20031389openalex-snapshot
Prevention of Autoimmunity by Targeting a Distinct, Noninvariant CD1d-reactive T Cell Population Reactive to Sulfatide
inferredcites →https://doi.org/10.1084/jem.20072484openalex-snapshot
The transcription factor NFATc2 controls IL-6–dependent T cell activation in experimental colitis
inferredcites →https://doi.org/10.1084/jem.20102555openalex-snapshot
Innate and cytokine-driven signals, rather than microbial antigens, dominate in natural killer T cell activation during microbial infection
inferredcites →https://doi.org/10.1084/jem.20102630openalex-snapshot
PLZF induces an intravascular surveillance program mediated by long-lived LFA-1–ICAM-1 interactions
inferredcites →https://doi.org/10.1084/jem.20110308openalex-snapshot
T cell receptor signal strength in Treg and iNKT cell development demonstrated by a novel fluorescent reporter mouse
inferredcites →https://doi.org/10.1084/jem.20130753openalex-snapshot
Paneth cell extrusion and release of antimicrobial products is directly controlled by immune cell–derived IFN-γ
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.1223490openalex-snapshot
Interactions Between the Microbiota and the Immune System
inferredcites →https://doi.org/10.1126/science.aaa4812openalex-snapshot
Group 3 innate lymphoid cells mediate intestinal selection of commensal bacteria–specific CD4 + T cells
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-2013-305671openalex-snapshot
IL-13Rα2-bearing, type II NKT cells reactive to sulfatide self-antigen populate the mucosa of ulcerative colitis
inferredcites →https://doi.org/10.1136/gutjnl-2014-308004openalex-snapshot
Tralokinumab for moderate-to-severe UC: a randomised, double-blind, placebo-controlled, phase IIa study
inferredcites →https://doi.org/10.1146/annurev-immunol-032414-112008openalex-snapshot
The Immunology of CD1- and MR1-Restricted T Cells
inferredcites →https://doi.org/10.1159/000467394openalex-snapshot
Human Invariant Natural Killer T Cells Respond to Antigen-Presenting Cells Exposed to Lipids from Olea europaea Pollen
inferredcites →https://doi.org/10.1172/jci19836openalex-snapshot
Nonclassical CD1d-restricted NK T cells that produce IL-13 characterize an atypical Th2 response in ulcerative colitis
inferredcites →https://doi.org/10.1172/jci36509openalex-snapshot
Cd1d-dependent regulation of bacterial colonization in the intestine of mice
inferredcites →https://doi.org/10.1172/jci72308openalex-snapshot
IL-10–producing NKT10 cells are a distinct regulatory invariant NKT cell subset
inferredcites →https://doi.org/10.1182/blood-2011-01-329268openalex-snapshot
IL-17–producing invariant NKT cells in lymphoid organs are recent thymic emigrants identified by neuropilin-1 expression
inferredcites →https://doi.org/10.1194/jlr.ra119000236openalex-snapshot
Bacterial immunogenic α-galactosylceramide identified in the murine large intestine: dependency on diet and inflammation
inferredcites →https://doi.org/10.1371/journal.pbio.1001610openalex-snapshot
Production of α-Galactosylceramide by a Prominent Member of the Human Gut Microbiota
inferredcites →https://doi.org/10.1371/journal.pbio.3000169openalex-snapshot
TLR9-mediated dendritic cell activation uncovers mammalian ganglioside species with specific ceramide backbones that activate invariant natural killer T cells
inferredcites →https://doi.org/10.15252/embj.201797537openalex-snapshot
CD1d‐mediated lipid presentation by CD11c+ cells regulates intestinal homeostasis
inferredcites →https://doi.org/10.15252/embj.2018101260openalex-snapshot
Transnuclear mice reveal Peyer's patch iNKT cells that regulate B‐cell class switching to IgG1
inferredcites →https://doi.org/10.15252/embr.201642412openalex-snapshot
CD1d‐mediated activation of group 3 innate lymphoid cells drives IL‐22 production
inferredcites →https://doi.org/10.26508/lsa.201800229openalex-snapshot
Mucosa-associated microbiota drives pathogenic functions in IBD-derived intestinal iNKT cells
inferredcites →https://doi.org/10.3389/fcimb.2018.00395openalex-snapshot
Targeting IL-13 as a Host-Directed Therapy Against Ulcerative Colitis
inferredcites →https://doi.org/10.3389/fimmu.2015.00316openalex-snapshot
Type II NKT Cells in Inflammation, Autoimmunity, Microbial Immunity, and Cancer
inferredcites →https://doi.org/10.3389/fimmu.2017.01447openalex-snapshot
Mixed Signals: Co-Stimulation in Invariant Natural Killer T Cell-Mediated Cancer Immunotherapy
inferredcites →https://doi.org/10.3389/fimmu.2018.00999openalex-snapshot
Invariant Natural Killer T Cells Shape the Gut Microbiota and Regulate Neutrophil Recruitment and Function During Intestinal Inflammation
inferredcites →https://doi.org/10.3389/fimmu.2018.02168openalex-snapshot
iNKT Cells Suppress Pathogenic NK1.1+CD8+ T Cells in DSS-Induced Colitis
inferredcites →https://doi.org/10.3389/fmed.2018.00021openalex-snapshot
Short-term Oral Antibiotics Treatment Promotes Inflammatory Activation of Colonic Invariant Natural Killer T and Conventional CD4+ T Cells
inferredcites →https://doi.org/10.4049/jimmunol.0902620openalex-snapshot
Commensal Microbiota and CD8+ T Cells Shape the Formation of Invariant NKT Cells
inferredcites →https://doi.org/10.4049/jimmunol.1000359openalex-snapshot
Identification of Regulatory Foxp3+ Invariant NKT Cells Induced by TGF-β
inferredcites →https://doi.org/10.4049/jimmunol.1102414openalex-snapshot
Distinct APCs Explain the Cytokine Bias of α-Galactosylceramide Variants In Vivo
inferredcites →https://doi.org/10.4049/jimmunol.1201010openalex-snapshot
Induced IL-17–Producing Invariant NKT Cells Require Activation in Presence of TGF-β and IL-1β
inferredcites →https://doi.org/10.4049/jimmunol.1400722openalex-snapshot
Antigen-Dependent versus -Independent Activation of Invariant NKT Cells during Infection
inferredcites →https://doi.org/10.4049/jimmunol.1403170openalex-snapshot
IL-9 Expression by Invariant NKT Cells Is Not Imprinted during Thymic Development
inferredcites →https://doi.org/10.4049/jimmunol.1501222openalex-snapshot
Antigen Specificity of Type I NKT Cells Is Governed by TCR β-Chain Diversity
inferredcites →https://doi.org/10.4049/jimmunol.1601410openalex-snapshot
NKT Cell–Deficient Mice Harbor an Altered Microbiota That Fuels Intestinal Inflammation during Chemically Induced Colitis
inferredcites →https://doi.org/10.4049/jimmunol.1601732openalex-snapshot
Roquin Paralogs Differentially Regulate Functional NKT Cell Subsets
inferredcites →https://doi.org/10.4049/jimmunol.180.4.2024openalex-snapshot
Cutting Edge: Activation by Innate Cytokines or Microbial Antigens Can Cause Arrest of Natural Killer T Cell Patrolling of Liver Sinusoids
inferredcites →https://doi.org/10.4049/jimmunol.196.supp.67.2openalex-snapshot
Group 3 innate lymphoid cells mediate intestinal selection of commensal bacteria-specific CD4+ T cells.
inferredcites →https://doi.org/10.7554/elife.34793openalex-snapshot
CCR7 defines a precursor for murine iNKT cells in thymus and periphery
inferredcites →https://doi.org/10.7554/elife.51663openalex-snapshot
Tissue-specific shaping of the TCR repertoire and antigen specificity of iNKT cells

What points at this work

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

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DJ-X-013 Reduces LPS-Induced Inflammation, Modulates Th17/ Myeloid-Derived Suppressor Cells, and Alters NF-kB Expression to Ameliorate Experimental Colitis
inferred← citeshttps://doi.org/10.1002/bies.70046openalex-snapshot
Butyrate, IL‐4, and EP4 Receptors: A Triad of Colorectal Homeostasis, Protecting Against Onset of Cancer and IBD?
inferred← citeshttps://doi.org/10.1007/s11302-023-09939-wopenalex-snapshot
The P2X7 receptor in mucosal adaptive immunity
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Role of microbiota-gut-brain axis in autoimmunity and multiple sclerosis
inferred← citeshttps://doi.org/10.1016/j.bbrc.2026.153347openalex-snapshot
Crohn's disease under single-cell map: from INFLARE metaplastic cells to rare immune cell subpopulations
inferred← citeshttps://doi.org/10.1016/j.biopha.2024.117379openalex-snapshot
DJ-X-013 reduces LPS-induced inflammation, modulates Th17/ myeloid-derived suppressor cells, and alters NF-κB expression to ameliorate experimental colitis
inferred← citeshttps://doi.org/10.1016/j.biopha.2026.119510openalex-snapshot
A novel microtubule inhibitor modulates the myeloid PD-L1 expression, restores T cell effector function, and promotes apoptosis for effective suppression of colorectal cancer
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114948openalex-snapshot
IFN-γ-dependent regulation of intestinal epithelial homeostasis by NKT cells
inferred← citeshttps://doi.org/10.1016/j.coi.2025.102676openalex-snapshot
Deciphering and harnessing gut microbiota–associated immune regulation in acute graft-versus-host disease
inferred← citeshttps://doi.org/10.1016/j.ebiom.2023.104788openalex-snapshot
Lower magnitude and faster waning of antibody responses to SARS-CoV-2 vaccination in anti-TNF-α-treated IBD patients are linked to lack of activation and expansion of cTfh1 cells and impaired B memory cell formation
inferred← citeshttps://doi.org/10.1016/j.humimm.2020.05.005openalex-snapshot
CD1 gene polymorphism and susceptibility to celiac disease: Association of CD1E*02/02 in Moroccans
inferred← citeshttps://doi.org/10.1016/j.intimp.2023.110666openalex-snapshot
The emerging paradigm of Unconventional T cells as a novel therapeutic target for celiac disease
inferred← citeshttps://doi.org/10.1016/j.intimp.2025.114462openalex-snapshot
Immune modulation for the patterns of epithelial cell death in inflammatory bowel disease
inferred← citeshttps://doi.org/10.1016/j.molimm.2024.03.011openalex-snapshot
CD1 molecules: Beyond antigen presentation
inferred← citeshttps://doi.org/10.1016/j.mucimm.2024.02.002openalex-snapshot
The intestinal microbiota modulates the transcriptional landscape of iNKT cells at steady-state and following antigen exposure
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.152212openalex-snapshot
Microplastic consumption induces inflammatory signatures in the colon and prolongs a viral arthritis
inferred← citeshttps://doi.org/10.1016/j.smim.2023.101816openalex-snapshot
Aging unconventionally: γδ T cells, iNKT cells, and MAIT cells in aging
inferred← citeshttps://doi.org/10.1016/j.taap.2026.117759openalex-snapshot
Interference with IL-13/JAK1/STAT6 inflammatory signaling by dipalmitoyl phosphoethanolamine-polyethylene glycol (DPPE-PEG); A CD1d-dependent antagonist to iNKT cells; contributes to retarding the advancement of oxazolone colitis
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5c00765openalex-snapshot
Significantly Boosted Th2-Selective Activity of NKT Cell Agonist Enabled by Sulfonamide Hydrogen-Bond Design
inferred← citeshttps://doi.org/10.1038/s12276-026-01831-yopenalex-snapshot
Microbial cues and T cell immunity: deciphering their interactions in chronic liver disease
inferred← citeshttps://doi.org/10.1111/all.15408openalex-snapshot
High‐dimensional immune profiles correlate with phenotypes of peanut allergy during food‐allergic reactions
inferred← citeshttps://doi.org/10.1111/imm.13401openalex-snapshot
Activated invariant natural killer T cells infiltrate aortic tissue as key participants in abdominal aortic aneurysm pathology
inferred← citeshttps://doi.org/10.1111/sji.13412openalex-snapshot
Dysregulation of T cell response in the pathogenesis of inflammatory bowel disease
inferred← citeshttps://doi.org/10.1155/2022/2939921openalex-snapshot
Biological Clock and Inflammatory Bowel Disease Review: From the Standpoint of the Intestinal Barrier
inferred← citeshttps://doi.org/10.1155/jimr/9743121openalex-snapshot
Research Progress on the Mechanism of Ginsenoside Rg1 in Inflammatory Bowel Disease
inferred← citeshttps://doi.org/10.1186/s12935-022-02557-3openalex-snapshot
From inflammatory bowel disease to colorectal cancer: what’s the role of miRNAs?
inferred← citeshttps://doi.org/10.15252/embj.2021107901openalex-snapshot
Calcium signals regulate the functional differentiation of thymic iNKT cells
inferred← citeshttps://doi.org/10.15789/2220-7619-dpp-2004openalex-snapshot
Disseminated purulent peritonitis outcome affects NKT cell phenotype
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Liposomal Co-Delivery of Antigenic Glycan LDNF and α-GalCer Elicits Potent IgG Responses with Potential for Anti-Helminth Immunity
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Revisiting an Expression Dataset of Discordant Inflammatory Bowel Disease Twin Pairs Using a Mutation Burden Test Reveals CYP2C18 as a Novel Marker
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Immunopathogenesis and immunoregulatory mechanisms in allergic contact dermatitis
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An Unconventional View of T Cell Reconstitution After Allogeneic Hematopoietic Cell Transplantation
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Early-Life Respiratory Syncytial Virus (RSV) Infection Triggers Immunological Changes in Gut-Associated Lymphoid Tissues in a Sex-Dependent Manner in Adulthood
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The iNKT Cell–Macrophage Axis in Homeostasis and Disease
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Effect of Hydrolyzed Frozen Meat on Diet Palatability, Apparent Digestibility, Immune Response, Fecal Microbiota, and Metabolome in British Shorthair Cats
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The Role of CD1 Gene Polymorphism in the Genetic Susceptibility to Spondyloarthropathies in the Moroccan Population and the Possible Cross-Link with Celiac Disease
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Effective Barriers: The Role of NKT Cells and Innate Lymphoid Cells in the Gut
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Characterization of MAIT TCR repertoire of gastrointestinal tract and peripheral blood MAIT cells
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Rôle des opioïdes d'origine immunitaire dans la physiologie intestinale
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The role of gut microbiota in T cell immunity and immune mediated disorders
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