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Induction of T cell anergy: integration of environmental cues and infectious tolerance
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1521-4141(200112)31:12<3737::aid-immu3737>3.0.co;2-gopenalex-snapshot
TCR engagement in the absence of cell cycle progression leads to T cell anergy independent of p27Kip1
inferredcites →https://doi.org/10.1002/eji.200636510openalex-snapshot
ICER/CREM‐mediated transcriptional attenuation of IL‐2 and its role in suppression by regulatory T cells
inferredcites →https://doi.org/10.1016/j.cell.2006.05.042openalex-snapshot
FOXP3 Controls Regulatory T Cell Function through Cooperation with NFAT
inferredcites →https://doi.org/10.1016/j.coi.2010.01.018openalex-snapshot
Metabolism in T cell activation and differentiation
inferredcites →https://doi.org/10.1016/j.immuni.2005.03.013openalex-snapshot
GCN2 Kinase in T Cells Mediates Proliferative Arrest and Anergy Induction in Response to Indoleamine 2,3-Dioxygenase
inferredcites →https://doi.org/10.1016/j.immuni.2007.07.008openalex-snapshot
Revving the Engine: Signal Transduction Fuels T Cell Activation
inferredcites →https://doi.org/10.1016/j.immuni.2008.09.018openalex-snapshot
Retinoic Acid Enhances Foxp3 Induction Indirectly by Relieving Inhibition from CD4+CD44hi Cells
inferredcites →https://doi.org/10.1016/j.immuni.2009.04.014openalex-snapshot
The mTOR Kinase Differentially Regulates Effector and Regulatory T Cell Lineage Commitment
inferredcites →https://doi.org/10.1016/j.immuni.2009.04.017openalex-snapshot
Deltex1 Is a Target of the Transcription Factor NFAT that Promotes T Cell Anergy
inferredcites →https://doi.org/10.1016/j.immuni.2010.05.002openalex-snapshot
The E3 Ubiquitin Ligase GRAIL Regulates T Cell Tolerance and Regulatory T Cell Function by Mediating T Cell Receptor-CD3 Degradation
inferredcites →https://doi.org/10.1016/j.it.2005.04.004openalex-snapshot
The ‘danger’ sensors that STOP the immune response: the A2 adenosine receptors?
inferredcites →https://doi.org/10.1016/j.it.2008.12.002openalex-snapshot
T regulatory cells: hypoxia-adenosinergic suppression and re-direction of the immune response
inferredcites →https://doi.org/10.1016/j.jdermsci.2009.02.001openalex-snapshot
Dendritic cells as controllers of antigen-specific Foxp3+ regulatory T cells
inferredcites →https://doi.org/10.1016/j.molimm.2008.09.029openalex-snapshot
IL-2 signaling prevents T cell anergy by inhibiting the expression of anergy-inducing genes
inferredcites →https://doi.org/10.1016/j.trim.2006.09.017openalex-snapshot
Tryptophan catabolism generates autoimmune-preventive regulatory T cells
inferredcites →https://doi.org/10.1038/356607a0openalex-snapshot
CD28-mediated signalling co-stimulates murine T cells and prevents induction of anergy in T-cell clones
inferredcites →https://doi.org/10.1038/nature05478openalex-snapshot
Foxp3 occupancy and regulation of key target genes during T-cell stimulation
inferredcites →https://doi.org/10.1038/nature05543openalex-snapshot
Foxp3-dependent programme of regulatory T-cell differentiation
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/ni.1835openalex-snapshot
CTLA-4 suppresses the pathogenicity of self antigen–specific T cells by cell-intrinsic and cell-extrinsic mechanisms
inferredcites →https://doi.org/10.1038/ni1047openalex-snapshot
Calcineurin imposes T cell unresponsiveness through targeted proteolysis of signaling proteins
inferredcites →https://doi.org/10.1038/ni1265openalex-snapshot
Inducing and expanding regulatory T cell populations by foreign antigen
inferredcites →https://doi.org/10.1038/ni1394openalex-snapshot
T cell anergy is reversed by active Ras and is regulated by diacylglycerol kinase-α
inferredcites →https://doi.org/10.1038/ni1549openalex-snapshot
Smad3 and NFAT cooperate to induce Foxp3 expression through its enhancer
inferredcites →https://doi.org/10.1038/ni1564openalex-snapshot
The E3 ubiquitin ligase Itch regulates expression of transcription factor Foxp3 and airway inflammation by enhancing the function of transcription factor TIEG1
inferredcites →https://doi.org/10.1038/ni1572openalex-snapshot
The Foxp3+ regulatory T cell: a jack of all trades, master of regulation
inferredcites →https://doi.org/10.1038/nm1449openalex-snapshot
TRAF6 is a T cell–intrinsic negative regulator required for the maintenance of immune homeostasis
inferredcites →https://doi.org/10.1038/nri1457openalex-snapshot
Ido expression by dendritic cells: tolerance and tryptophan catabolism
inferredcites →https://doi.org/10.1038/nri1710openalex-snapshot
Fuel feeds function: energy metabolism and the T-cell response
inferredcites →https://doi.org/10.1038/nri2546openalex-snapshot
Immunoregulatory functions of mTOR inhibition
inferredcites →https://doi.org/10.1073/pnas.0800928105openalex-snapshot
T cell receptor signaling controls Foxp3 expression via PI3K, Akt, and mTOR
inferredcites →https://doi.org/10.1073/pnas.0903919106openalex-snapshot
Infectious tolerance via the consumption of essential amino acids and mTOR signaling
inferredcites →https://doi.org/10.1073/pnas.0910341107openalex-snapshot
Dual function of CTLA-4 in regulatory T cells and conventional T cells to prevent multiorgan autoimmunity
inferredcites →https://doi.org/10.1074/jbc.m604192200openalex-snapshot
GRAIL Is Up-regulated in CD4+ CD25+ T Regulatory Cells and Is Sufficient for Conversion of T Cells to a Regulatory Phenotype
inferredcites →https://doi.org/10.1084/jem.165.2.302openalex-snapshot
Antigen presentation by chemically modified splenocytes induces antigen-specific T cell unresponsiveness in vitro and in vivo.
inferredcites →https://doi.org/10.1084/jem.192.2.303openalex-snapshot
Immunologic Self-Tolerance Maintained by Cd25+Cd4+Regulatory T Cells Constitutively Expressing Cytotoxic T Lymphocyte–Associated Antigen 4
inferredcites →https://doi.org/10.1084/jem.20030152openalex-snapshot
Conversion of Peripheral CD4+CD25− Naive T Cells to CD4+CD25+ Regulatory T Cells by TGF-β Induction of Transcription Factor Foxp3
inferredcites →https://doi.org/10.1084/jem.20040249openalex-snapshot
In Vivo Instruction of Suppressor Commitment in Naive T Cells
inferredcites →https://doi.org/10.1084/jem.20041538openalex-snapshot
NFATc2 and NFATc3 transcription factors play a crucial role in suppression of CD4+ T lymphocytes by CD4+ CD25+ regulatory T cells
inferredcites →https://doi.org/10.1084/jem.20062512openalex-snapshot
Adenosine generation catalyzed by CD39 and CD73 expressed on regulatory T cells mediates immune suppression
inferredcites →https://doi.org/10.1084/jem.20070590openalex-snapshot
A functionally specialized population of mucosal CD103+ DCs induces Foxp3+ regulatory T cells via a TGF-β– and retinoic acid–dependent mechanism
inferredcites →https://doi.org/10.1084/jem.20070602openalex-snapshot
Small intestine lamina propria dendritic cells promote de novo generation of Foxp3 T reg cells via retinoic acid
inferredcites →https://doi.org/10.1084/jem.20071477openalex-snapshot
The AKT–mTOR axis regulates de novo differentiation of CD4+Foxp3+ cells
inferredcites →https://doi.org/10.1084/jem.20081811openalex-snapshot
CD4+ regulatory T cells require CTLA-4 for the maintenance of systemic tolerance
inferredcites →https://doi.org/10.1084/jem.20090639openalex-snapshot
Retinoic acid can enhance conversion of naive into regulatory T cells independently of secreted cytokines
inferredcites →https://doi.org/10.1126/science.1145697openalex-snapshot
Reciprocal T H 17 and Regulatory T Cell Differentiation Mediated by Retinoic Acid
inferredcites →https://doi.org/10.1126/science.1160062openalex-snapshot
CTLA-4 Control over Foxp3 + Regulatory T Cell Function
inferredcites →https://doi.org/10.1126/science.271.5253.1272openalex-snapshot
Blocked Signal Transduction to the ERK and JNK Protein Kinases in Anergic CD4 + T Cells
inferredcites →https://doi.org/10.1146/annurev.immunol.21.120601.141110openalex-snapshot
T Cell Anergy
inferredcites →https://doi.org/10.1182/blood-2006-12-064527openalex-snapshot
Expression of ectonucleotidase CD39 by Foxp3+ Treg cells: hydrolysis of extracellular ATP and immune suppression
inferredcites →https://doi.org/10.1182/blood-2007-03-081646openalex-snapshot
A2A receptor signaling promotes peripheral tolerance by inducing T-cell anergy and the generation of adaptive regulatory T cells
inferredcites →https://doi.org/10.1182/blood-2007-05-088831openalex-snapshot
Dendritic cells are specialized accessory cells along with TGF-β for the differentiation of Foxp3+ CD4+ regulatory T cells from peripheral Foxp3− precursors
inferredcites →https://doi.org/10.1182/blood-2009-09-245274openalex-snapshot
Skin-draining lymph nodes contain dermis-derived CD103− dendritic cells that constitutively produce retinoic acid and induce Foxp3+ regulatory T cells
inferredcites →https://doi.org/10.1189/jlb.1207851openalex-snapshot
De novo induction of antigen-specific CD4+CD25+Foxp3+ regulatory T cells in vivo following systemic antigen administration accompanied by blockade of mTOR
inferredcites →https://doi.org/10.4049/jimmunol.0803510openalex-snapshot
Anergic T Cells Are Metabolically Anergic
inferredcites →https://doi.org/10.4049/jimmunol.0803917openalex-snapshot
New Insights into the Molecular Basis of T Cell Anergy: Anergy Factors, Avoidance Sensors, and Epigenetic Imprinting
inferredcites →https://doi.org/10.4049/jimmunol.0803986openalex-snapshot
Naive CD4 T Cell Proliferation Is Controlled by Mammalian Target of Rapamycin Regulation of GRAIL Expression
inferredcites →https://doi.org/10.4049/jimmunol.138.11.3704openalex-snapshot
Stimulation of normal inducer T cell clones with antigen presented by purified Ia molecules in planar lipid membranes: specific induction of a long-lived state of proliferative nonresponsiveness.
inferredcites →https://doi.org/10.4049/jimmunol.162.5.2775openalex-snapshot
Inhibition of Cell Cycle Progression by Rapamycin Induces T Cell Clonal Anergy Even in the Presence of Costimulation
inferredcites →https://doi.org/10.4049/jimmunol.172.8.4797openalex-snapshot
The Novel Cyclophilin Binding Compound, Sanglifehrin A, Disassociates G1 Cell Cycle Arrest from Tolerance Induction
inferredcites →https://doi.org/10.4049/jimmunol.173.2.1059openalex-snapshot
Resistance to CD4+CD25+ Regulatory T Cells and TGF-β in Cbl-b−/− Mice
inferredcites →https://doi.org/10.4049/jimmunol.176.11.6752openalex-snapshot
The Combined Effects of Tryptophan Starvation and Tryptophan Catabolites Down-Regulate T Cell Receptor ζ-Chain and Induce a Regulatory Phenotype in Naive T Cells
inferredcites →https://doi.org/10.4049/jimmunol.176.3.1316openalex-snapshot
Cutting Edge: Deficiency in the E3 Ubiquitin Ligase Cbl-b Results in a Multifunctional Defect in T Cell TGF-β Sensitivity In Vitro and In Vivo
inferredcites →https://doi.org/10.4049/jimmunol.178.4.2163openalex-snapshot
A Role for Mammalian Target of Rapamycin in Regulating T Cell Activation versus Anergy
inferredcites →https://doi.org/10.4049/jimmunol.178.7.4022openalex-snapshot
Cutting Edge: IL-2 Is Essential for TGF-β-Mediated Induction of Foxp3+ T Regulatory Cells
inferredcites →https://doi.org/10.4049/jimmunol.180.1.34openalex-snapshot
Cutting Edge: Requirement for TRAF6 in the Induction of T Cell Anergy
inferredcites →https://doi.org/10.4049/jimmunol.181.10.6923openalex-snapshot
CD8+CD205+ Splenic Dendritic Cells Are Specialized to Induce Foxp3+ Regulatory T Cells
inferredcites →https://doi.org/10.4161/cc.6.22.4933openalex-snapshot
The Gcn2 Kinase as a Cell Cycle Regulator
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9780470015902.a0000950.pub3openalex-snapshot
Immunological Tolerance: Mechanisms
inferred← citeshttps://doi.org/10.1002/art.38015openalex-snapshot
Premature Cell Senescence and T Cell Receptor–Independent Activation of CD8+ T Cells in Juvenile Idiopathic Arthritis
inferred← citeshttps://doi.org/10.1002/eji.201142307openalex-snapshot
Silencing of the I l2 gene transcription is regulated by epigenetic changes in anergic T cells
inferred← citeshttps://doi.org/10.1002/eji.201646572openalex-snapshot
Increased endogenous antigen presentation in the periphery enhances susceptibility to inflammation‐induced gastric autoimmunity in mice
inferred← citeshttps://doi.org/10.1002/eji.70192openalex-snapshot
CD8 T Cell Sensing of Type I Interferon Impacts Anergy
inferred← citeshttps://doi.org/10.1002/jat.3100openalex-snapshot
Toxicity of cobalt–chromium nanoparticles released from a resurfacing hip implant and cobalt ions on primary human lymphocytes in vitro
inferred← citeshttps://doi.org/10.1007/978-1-4939-2071-6_15openalex-snapshot
Mixed Chimerism for Tolerance Induction of Vascularized Composite Allografts
inferred← citeshttps://doi.org/10.1007/s00018-011-0907-zopenalex-snapshot
The battle against immunopathology: infectious tolerance mediated by regulatory T cells
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A stepwise model of polyreactivity of the T cell antigen-receptor (TCR): its impact on the self–nonself discrimination and on related observations (receptor editing, anergy, dual receptor cells)
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The Human Immune Response
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T-Cell Activation and Tolerance
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The Human Immune Response
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T-Cell Activation and Tolerance
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The human immune response
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T-cell activation and tolerance
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Dendritic cells and antigen-specific immunotherapy in autoimmune rheumatic diseases
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The link between small heat shock proteins and the immune system
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Autophagy Is a Tolerance-Avoidance Mechanism that Modulates TCR-Mediated Signaling and Cell Metabolism to Prevent Induction of T Cell Anergy
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Dynamic Adoption of Anergy by Antigen-Exhausted CD4 + T Cells
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IRF4 impedes human CD8 T cell function and promotes cell proliferation and PD-1 expression
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Langerhans cells from women with cervical precancerous lesions become functionally responsive against human papillomavirus after activation with stabilized Poly-I:C
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Antigen-based immunotherapy (AIT) for autoimmune and allergic disease
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Dynamics of immune parameters during the treatment of active tuberculosis showing negative interferon gamma response at the time of diagnosis
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T cells in helminth infection: the regulators and the regulated
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The three main stumbling blocks for anticancer T cells
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The Proteomic Profile of Adults With a Fontan Circulation
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Therapeutic reversal of food allergen sensitivity by mature retinoic acid–differentiated dendritic cell induction of LAG3+CD49b−Foxp3− regulatory T cells
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Immune adjuvants as critical guides directing immunity triggered by therapeutic cancer vaccines
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Association between tuberculosis recurrence and interferon-γ response during treatment
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Diagnostic accuracy of the interferon-gamma release assay (IGRA) for cases of feline mycobacteriosis
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T cell ignorance is bliss: T cells are not tolerized by Langerhans cells presenting human papillomavirus antigens in the absence of costimulation
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Food allergy in adults. Is there a difference between HIV and non-HIV patients?
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Induction and stability of the anergic phenotype in T cells
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Treatment of Experimental Autoimmune Encephalomyelitis by Codelivery of Disease Associated Peptide and Dexamethasone in Acetalated Dextran Microparticles
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SOCS1 Prevents Potentially Skin-Reactive Cytotoxic T Lymphocytes from Gaining the Ability to Cause Inflammatory Lesions
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IFN-γ-induced iNOS Expression in Mouse Regulatory Macrophages Prolongs Allograft Survival in Fully Immunocompetent Recipients
inferred← citeshttps://doi.org/10.1038/ni.3036openalex-snapshot
TLR7 induces anergy in human CD4+ T cells
inferred← citeshttps://doi.org/10.1038/ni.3331openalex-snapshot
CD4+ T cell anergy prevents autoimmunity and generates regulatory T cell precursors
inferred← citeshttps://doi.org/10.1038/s41385-020-00349-4openalex-snapshot
Self and microbiota-derived epitopes induce CD4+ T cell anergy and conversion into CD4+Foxp3+ regulatory cells
inferred← citeshttps://doi.org/10.1038/s41590-023-01444-xopenalex-snapshot
A single-amino acid substitution in the adaptor LAT accelerates TCR proofreading kinetics and alters T-cell selection, maintenance and function
inferred← citeshttps://doi.org/10.1038/s41590-024-02021-6openalex-snapshot
PD-1 and CD73 on naive CD4+ T cells synergistically limit responses to self
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Mechanistic insights into silica nanoparticle–allergen interactions on antigen presenting cell function in the context of allergic reactions
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Anti-CCR4 mAb selectively depletes effector-type FoxP3 + CD4 + regulatory T cells, evoking antitumor immune responses in humans
inferred← citeshttps://doi.org/10.1073/pnas.1401115111openalex-snapshot
Local immunostimulation leading to rejection of accepted male skin grafts by female mice as a model for cancer immunotherapy
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Tolerance induction in memory CD4 T cells requires two rounds of antigen-specific activation
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Targeting the CTLA-4/B7 axes in glioblastoma: preclinical evidence and clinical interventions
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Congenital B cell lymphocytosis explained by novel germline CARD11 mutations
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NFAT-dependent and -independent exhaustion circuits program maternal CD8 T cell hypofunction in pregnancy
inferred← citeshttps://doi.org/10.1084/jem.20230183openalex-snapshot
BATF represses BIM to sustain tolerant T cells in the periphery
inferred← citeshttps://doi.org/10.1089/aid.2018.0105openalex-snapshot
CD4 + T Cell Subsets and Pathways to HIV Latency
inferred← citeshttps://doi.org/10.1093/infdis/jiv071openalex-snapshot
Functional Exhaustion Limits CD4+and CD8+T-Cell Responses to Congenital Cytomegalovirus Infection
inferred← citeshttps://doi.org/10.1101/cshperspect.a006957openalex-snapshot
T-Cell Tolerance: Central and Peripheral
inferred← citeshttps://doi.org/10.1111/aji.12806openalex-snapshot
Characterization of CD 127− CD 25++ Treg from human colostrum
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Intranasal peptide‐induced tolerance and linked suppression: consequences of complement deficiency
inferred← citeshttps://doi.org/10.1111/imm.13302openalex-snapshot
The cytosolic tryparedoxin peroxidase from Trypanosoma cruzi induces a pro‐inflammatory Th1 immune response in a peroxidatic cysteine‐dependent manner
inferred← citeshttps://doi.org/10.1111/j.1600-065x.2012.01152.xopenalex-snapshot
mTOR , metabolism, and the regulation of T‐cell differentiation and function
inferred← citeshttps://doi.org/10.1111/petr.13795openalex-snapshot
The immune system in infants: Relevance to xenotransplantation
inferred← citeshttps://doi.org/10.1113/jphysiol.2012.233221openalex-snapshot
Regulation of lymphocyte function by ORAI and STIM proteins in infection and autoimmunity
inferred← citeshttps://doi.org/10.1126/science.aaa1292openalex-snapshot
Detection of self-reactive CD8 + T cells with an anergic phenotype in healthy individuals
inferred← citeshttps://doi.org/10.1134/s000629791302003xopenalex-snapshot
Molecular mechanisms of T-cell anergy
inferred← citeshttps://doi.org/10.1146/annurev-pharmtox-022820-093805openalex-snapshot
Clinical Pharmacology and Interplay of Immune Checkpoint Agents: A Yin-Yang Balance
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A Role for Folate in Microbiome-Linked Control of Autoimmunity
inferred← citeshttps://doi.org/10.1158/1078-0432.ccr-13-2627openalex-snapshot
Multifactorial T-cell Hypofunction That Is Reversible Can Limit the Efficacy of Chimeric Antigen Receptor–Transduced Human T cells in Solid Tumors
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Blockade of Programmed Death 1 Augments the Ability of Human T Cells Engineered to Target NY-ESO-1 to Control Tumor Growth after Adoptive Transfer
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Dendritic cells and their role in tumor immunosurveillance
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Rational combinations of immunotherapeutics that target discrete pathways
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The role of the adaptive immune system and T cell dysfunction in neurodegenerative diseases
inferred← citeshttps://doi.org/10.1186/s13045-018-0629-xopenalex-snapshot
T cell senescence and CAR-T cell exhaustion in hematological malignancies
inferred← citeshttps://doi.org/10.1189/jlb.2hi0815-334ropenalex-snapshot
Human regulatory T cells control TCR signaling and susceptibility to suppression in CD4+ T cells
inferred← citeshttps://doi.org/10.12688/f1000research.16551.1openalex-snapshot
Anergy into T regulatory cells: an integration of metabolic cues and epigenetic changes at the Foxp3 conserved non-coding sequence 2
inferred← citeshttps://doi.org/10.1371/journal.pntd.0002136openalex-snapshot
Modulation of Innate Antigen-Presenting Cell Function by Pre-patent Schistosome Infection
inferred← citeshttps://doi.org/10.1371/journal.pntd.0002567openalex-snapshot
Impairment of T Cell Function in Parasitic Infections
inferred← citeshttps://doi.org/10.1371/journal.pntd.0005307openalex-snapshot
GRAIL and Otubain-1 are Related to T Cell Hyporesponsiveness during Trypanosoma cruzi Infection
inferred← citeshttps://doi.org/10.1371/journal.pone.0139019openalex-snapshot
GIMAP5 Deficiency Is Associated with Increased AKT Activity in T Lymphocytes
inferred← citeshttps://doi.org/10.1371/journal.ppat.1006425openalex-snapshot
Aberrant plasma IL-7 and soluble IL-7 receptor levels indicate impaired T-cell response to IL-7 in human tuberculosis
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Brain Glycolipids Suppress T Helper Cells and Inhibit Autoimmune Demyelination
inferred← citeshttps://doi.org/10.17169/refubium-17290openalex-snapshot
Signalwege von Sphingosin-1-Phosphat und deren Bedeutung für die endozytotische Aktivität von Dendritischen Zellen
inferred← citeshttps://doi.org/10.2174/187152712801661293openalex-snapshot
Mechanisms in the Development of Multiple Sclerosis Lesions: Reconciling Autoimmune and Neurodegenerative Factors
inferred← citeshttps://doi.org/10.26686/wgtn.17005993openalex-snapshot
Type II Activation of Macrophages and Microglia: Roles in T cell biasing and experimental autoimmune encephalomyelitis
inferred← citeshttps://doi.org/10.3109/08830185.2013.829468openalex-snapshot
Current Status of Allograft Tolerance in Intestinal Transplantation
inferred← citeshttps://doi.org/10.33549/physiolres.935296openalex-snapshot
Maternal-Fetal Microchimerism: Impacts on Offspring's Immune Development and Transgenerational Immune Memory Transfer
inferred← citeshttps://doi.org/10.3389/fcell.2016.00130openalex-snapshot
Diacylglycerol Kinases in T Cell Tolerance and Effector Function
inferred← citeshttps://doi.org/10.3389/fimmu.2013.00178openalex-snapshot
Regulation of Lipid Signaling by Diacylglycerol Kinases during T Cell Development and Function
inferred← citeshttps://doi.org/10.3389/fimmu.2014.00051openalex-snapshot
Lymphopenia-Induced Proliferation in Aire-Deficient Mice Helps to Explain Their Autoimmunity and Differences from Human Patients
inferred← citeshttps://doi.org/10.3389/fimmu.2018.03017openalex-snapshot
A Computational Approach Identifies Immunogenic Features of Prognosis in Human Cancers
inferred← citeshttps://doi.org/10.3389/fimmu.2020.575451openalex-snapshot
Mannan-MOG35-55 Reverses Experimental Autoimmune Encephalomyelitis, Inducing a Peripheral Type 2 Myeloid Response, Reducing CNS Inflammation, and Preserving Axons in Spinal Cord Lesions
inferred← citeshttps://doi.org/10.3389/fimmu.2020.608377openalex-snapshot
Immune Privilege: The Microbiome and Uveitis
inferred← citeshttps://doi.org/10.3389/fimmu.2022.849012openalex-snapshot
Human Breast Milk: From Food to Active Immune Response With Disease Protection in Infants and Mothers
inferred← citeshttps://doi.org/10.3389/fimmu.2022.871372openalex-snapshot
Population pharmacokinetic models of anti-PD-1 mAbs in patients with multiple tumor types: A systematic review
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1542380openalex-snapshot
Nanoparticle platform preferentially targeting liver sinusoidal endothelial cells induces tolerance in CD4+ T cell-mediated disease models
inferred← citeshttps://doi.org/10.3389/fonc.2023.1088129openalex-snapshot
Yin and yang roles of B lymphocytes in solid tumors: Balance between antitumor immunity and immune tolerance/immunosuppression in tumor-draining lymph nodes
inferred← citeshttps://doi.org/10.33915/etd.5874openalex-snapshot
An Overview of Acute Myeloid Leukemia and Cancer Immunology: (i) Concepts and Therapeutic Strategies and (ii) RepSox as a Candidate Cell-Engineering Tool
inferred← citeshttps://doi.org/10.3892/ol.2020.12121openalex-snapshot
Hydrogen gas activates coenzyme Q10 to restore exhausted CD8+ T cells, especially PD‑1+Tim3+terminal CD8+ T cells, leading to better nivolumab outcomes in patients with lung cancer
inferred← citeshttps://doi.org/10.4049/jimmunol.1102307openalex-snapshot
Antigen Targeting to Plasmacytoid Dendritic Cells via Siglec-H Inhibits Th Cell-Dependent Autoimmunity
inferred← citeshttps://doi.org/10.4049/jimmunol.1301416openalex-snapshot
Deltex1 Promotes Protein Kinase Cθ Degradation and Sustains Casitas B-Lineage Lymphoma Expression
inferred← citeshttps://doi.org/10.4049/jimmunol.1400567openalex-snapshot
Cellular Mechanisms of CCL22-Mediated Attenuation of Autoimmune Diabetes
inferred← citeshttps://doi.org/10.4049/jimmunol.1500710openalex-snapshot
Mannose-Capped Lipoarabinomannan from Mycobacterium tuberculosis Induces CD4+ T Cell Anergy via GRAIL
inferred← citeshttps://doi.org/10.4049/jimmunol.1602031openalex-snapshot
Relationship between CD4 Regulatory T Cells and Anergy In Vivo
inferred← citeshttps://doi.org/10.4049/jimmunol.2001315openalex-snapshot
Revisiting Current Concepts on the Tolerogenicity of Steady-State Dendritic Cell Subsets and Their Maturation Stages
inferred← citeshttps://doi.org/10.4110/in.2022.22.e50openalex-snapshot
Low-Level Expression of CD138 Marks Naturally Arising Anergic B Cells
inferred← citeshttps://doi.org/10.4161/cc.22235openalex-snapshot
An expanded role of the tumor suppressor TSC1 in T cell tolerance
inferred← citeshttps://doi.org/10.58854/jicm.1537863openalex-snapshot
Transplantasyonda Tolerans Oluşturma Stratejileri ve İmmün Mekanizmalar
inferred← citeshttps://doi.org/10.70675/1dcb97a5za482z4664zaaf6z62a53817eea9openalex-snapshot
Défauts fonctionnels des cellules NK en contexte de stimulation chronique
inferred← citeshttps://doi.org/10.70675/ee25faf6za45bz4bbfzb67fzc8a5a7712c63openalex-snapshot
Induction de sous-populations de cellules dendritiques humaines pro-tolérogènes par des fragments d’anticorps bispécifiques
inferred← citeshttps://doi.org/10.70675/f02ecd8az6eeaz41f7zbdf9z0d1fbb9b530aopenalex-snapshot
Rôle de l’activation des cellules « Natural Killer » par le « missing self » dans la génération de lésions de rejet vasculaire chronique après transplantation d’organe
inferred← citeshttps://doi.org/10.7554/elife.26423openalex-snapshot
High mTOR activity is a hallmark of reactive natural killer cells and amplifies early signaling through activating receptors
inferred← citeshttps://doi.org/10.7554/elife.96812openalex-snapshot
Neurotrophic factor Neuritin modulates T cell electrical and metabolic state for the balance of tolerance and immunity
inferred← citeshttps://doi.org/10.7554/elife.96812.1openalex-snapshot
Neurotrophic factor Neuritin modulates T cell electrical and metabolic state for the balance of tolerance and immunity
inferred← citeshttps://doi.org/10.7554/elife.96812.1.sa0openalex-snapshot
Reviewer #2 (Public Review): Neurotrophic factor Neuritin modulates T cell electrical and metabolic state for the balance of tolerance and immunity
inferred← citeshttps://doi.org/10.7554/elife.96812.1.sa1openalex-snapshot
Reviewer #1 (Public Review): Neurotrophic factor Neuritin modulates T cell electrical and metabolic state for the balance of tolerance and immunity
inferred← citeshttps://doi.org/10.7554/elife.96812.1.sa2openalex-snapshot
eLife Assessment: Neurotrophic factor Neuritin modulates T cell electrical and metabolic state for the balance of tolerance and immunity
inferred← citeshttps://doi.org/10.7554/elife.96812.1.sa3openalex-snapshot
Author response: Neurotrophic factor Neuritin modulates T cell electrical and metabolic state for the balance of tolerance and immunity
inferred← citeshttps://doi.org/10.7554/elife.96812.2openalex-snapshot
Neurotrophic factor Neuritin modulates T cell electrical and metabolic state for the balance of tolerance and immunity
inferred← citeshttps://doi.org/10.7554/elife.96812.3openalex-snapshot
Neurotrophic factor Neuritin modulates T cell electrical and metabolic state for the balance of tolerance and immunity
inferred← citeshttps://doi.org/10.7936/k72z13hvopenalex-snapshot
MHC Class I-Dependent Acquisition and Maintenance of Natural Killer Cell Function
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