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NADPH Oxidase 2 Interaction with TLR2 Is Required for Efficient Innate Immune Responses to Mycobacteria via Cathelicidin Expression
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Global epidemiology of tuberculosis. Morbidity and mortality of a worldwide epidemic
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Regulation of the human neutrophil NADPH oxidase by the Rac GTP-binding proteins
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Redox control of cell fate by MAP kinase: physiological roles of ASK1-MAP kinase pathway in stress signaling
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LL-37, the only human member of the cathelicidin family of antimicrobial peptides
inferredcites →https://doi.org/10.1016/j.cardiores.2006.09.012openalex-snapshot
Role of NADPH oxidase 4 in lipopolysaccharide-induced proinflammatory responses by human aortic endothelial cells
inferredcites →https://doi.org/10.1016/j.cell.2006.05.035openalex-snapshot
NOX2 Controls Phagosomal pH to Regulate Antigen Processing during Crosspresentation by Dendritic Cells
inferredcites →https://doi.org/10.1016/j.tube.2005.08.021openalex-snapshot
Innate immunity to mycobacterial infection in mice: Critical role for toll-like receptors
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Growth of Mycobacterium bovis, Bacille Calmette-Guérin, within human monocytes-macrophages cultured in serum-free medium
inferredcites →https://doi.org/10.1016/s0140-6736(06)68384-0openalex-snapshot
Global epidemiology of tuberculosis
inferredcites →https://doi.org/10.1016/s0968-0004(03)00194-4openalex-snapshot
NADPH oxidases: not just for leukocytes anymore!
inferredcites →https://doi.org/10.1038/ni1200openalex-snapshot
ROS-dependent activation of the TRAF6-ASK1-p38 pathway is selectively required for TLR4-mediated innate immunity
inferredcites →https://doi.org/10.1038/nri1312openalex-snapshot
NOX enzymes and the biology of reactive oxygen
inferredcites →https://doi.org/10.1074/jbc.m102876200openalex-snapshot
1α,25-Dihydroxyvitamin D3-induced Monocyte Antimycobacterial Activity Is Regulated by Phosphatidylinositol 3-Kinase and Mediated by the NADPH-dependent Phagocyte Oxidase
inferredcites →https://doi.org/10.1084/jem.175.4.1111openalex-snapshot
Killing of virulent Mycobacterium tuberculosis by reactive nitrogen intermediates produced by activated murine macrophages.
inferredcites →https://doi.org/10.1089/ars.2006.8.1533openalex-snapshot
Regulation of the Phagocyte NADPH Oxidase by Rac GTPase
inferredcites →https://doi.org/10.1097/00062752-200201000-00003openalex-snapshot
Nox/Duox family of nicotinamide adenine dinucleotide (phosphate) oxidases
inferredcites →https://doi.org/10.1097/01.asn.0000077404.45564.7eopenalex-snapshot
Cellular Regulation by Hydrogen Peroxide
inferredcites →https://doi.org/10.1097/inf.0b013e31815b494copenalex-snapshot
Susceptibility to Mycobacterial Infections in Children With X-Linked Chronic Granulomatous Disease
inferredcites →https://doi.org/10.1111/j.1365-2133.2007.08196.xopenalex-snapshot
Cathelicidin LL-37 induces the generation of reactive oxygen species and release of human α-defensins from neutrophils
inferredcites →https://doi.org/10.1111/j.1462-5822.2006.00699.xopenalex-snapshot
Intracellular network of phosphatidylinositol 3-kinase, mammalian target of the rapamycin/70 kDa ribosomal S6 kinase 1, and mitogen-activated protein kinases pathways for regulating mycobacteria-induced IL-23 expression in human macrophages
inferredcites →https://doi.org/10.1111/j.1462-5822.2006.00797.xopenalex-snapshot
Protein kinase C zeta plays an essential role for Mycobacterium tuberculosis-induced extracellular signal-regulated kinase 1/2 activation in monocytes/macrophages via Toll-like receptor 2
inferredcites →https://doi.org/10.1111/j.1462-5822.2007.00914.xopenalex-snapshot
Intracellular signalling cascades regulating innate immune responses to Mycobacteria: branching out from Toll-like receptors
inferredcites →https://doi.org/10.1111/j.1462-5822.2007.01081.xopenalex-snapshot
ASK1-p38 MAPK-p47phox activation is essential for inflammatory responses during tuberculosis via TLR2-ROS signalling
inferredcites →https://doi.org/10.1111/j.1462-5822.2008.01179.xopenalex-snapshot
Mycobacterium tuberculosislipoprotein-induced association of TLR2 with protein kinase C ζ in lipid rafts contributes to reactive oxygen species-dependent inflammatory signalling in macrophages
inferredcites →https://doi.org/10.1126/science.1123933openalex-snapshot
Toll-Like Receptor Triggering of a Vitamin D-Mediated Human Antimicrobial Response
inferredcites →https://doi.org/10.1126/science.1130481openalex-snapshot
H 2 O 2 , a Necessary Evil for Cell Signaling
inferredcites →https://doi.org/10.1128/cdli.5.5.690-694.1998openalex-snapshot
Diminished Adherence and/or Ingestion of VirulentMycobacterium tuberculosisby Monocyte-Derived Macrophages from Patients with Tuberculosis
inferredcites →https://doi.org/10.1128/iai.01218-07openalex-snapshot
Expression of Cathelicidin LL-37 duringMycobacterium tuberculosisInfection in Human Alveolar Macrophages, Monocytes, Neutrophils, and Epithelial Cells
inferredcites →https://doi.org/10.1128/iai.63.4.1291-1297.1995openalex-snapshot
Human CAP18: a novel antimicrobial lipopolysaccharide-binding protein
inferredcites →https://doi.org/10.1136/bmj.1.4548.430openalex-snapshot
Vitamin D in Treatment of Cutaneous Tuberculosis
inferredcites →https://doi.org/10.1146/annurev.immunol.20.081501.125851openalex-snapshot
Genetic Dissection of Immunity to Mycobacteria: The Human Model
inferredcites →https://doi.org/10.1161/01.res.74.6.1141openalex-snapshot
Angiotensin II stimulates NADH and NADPH oxidase activity in cultured vascular smooth muscle cells.
inferredcites →https://doi.org/10.1172/jci200318174openalex-snapshot
Specificity of a third kind: reactive oxygen and nitrogen intermediates in cell signaling
inferredcites →https://doi.org/10.1182/blood-2006-05-024406openalex-snapshot
The β-glucan receptor dectin-1 functions together with TLR2 to mediate macrophage activation by mycobacteria
inferredcites →https://doi.org/10.1189/jlb.1206763openalex-snapshot
Crosstalk among Jak-STAT, Toll-like receptor, and ITAM-dependent pathways in macrophage activation
inferredcites →https://doi.org/10.1371/journal.ppat.0030110openalex-snapshot
Mycobacterium tuberculosis nuoG Is a Virulence Gene That Inhibits Apoptosis of Infected Host Cells
inferredcites →https://doi.org/10.1615/critrevimmunol.v26.i6.60openalex-snapshot
Human Defensins and Cathelicidins in the Skin: Beyond Direct Antimicrobial Properties
inferredcites →https://doi.org/10.4049/jimmunol.169.7.3883openalex-snapshot
The Human Antimicrobial Peptide LL-37 Is a Multifunctional Modulator of Innate Immune Responses
inferredcites →https://doi.org/10.4049/jimmunol.171.12.6690openalex-snapshot
The Antimicrobial Peptide LL-37 Activates Innate Immunity at the Airway Epithelial Surface by Transactivation of the Epidermal Growth Factor Receptor
inferredcites →https://doi.org/10.4049/jimmunol.172.4.2522openalex-snapshot
Involvement of Reactive Oxygen Species in Toll-Like Receptor 4-Dependent Activation of NF-κB
inferredcites →https://doi.org/10.4049/jimmunol.173.6.3589openalex-snapshot
Cutting Edge: Direct Interaction of TLR4 with NAD(P)H Oxidase 4 Isozyme Is Essential for Lipopolysaccharide-Induced Production of Reactive Oxygen Species and Activation of NF-κB
inferredcites →https://doi.org/10.4049/jimmunol.173.9.5749openalex-snapshot
Toll Receptor-Mediated Regulation of NADPH Oxidase in Human Dendritic Cells
inferredcites →https://doi.org/10.4049/jimmunol.174.7.4271openalex-snapshot
Structure-Function Relationships among Human Cathelicidin Peptides: Dissociation of Antimicrobial Properties from Host Immunostimulatory Activities
inferredcites →https://doi.org/10.4049/jimmunol.177.3.1864openalex-snapshot
Macrophages Acquire Neutrophil Granules for Antimicrobial Activity against Intracellular Pathogens
inferredcites →https://doi.org/10.4049/jimmunol.178.11.7190openalex-snapshot
IFN-γ- and TNF-Independent Vitamin D-Inducible Human Suppression of Mycobacteria: The Role of Cathelicidin LL-37
inferredcites →https://doi.org/10.4049/jimmunol.179.11.7684openalex-snapshot
Host Defense Peptide LL-37, in Synergy with Inflammatory Mediator IL-1β, Augments Immune Responses by Multiple Pathways
inferredcites →https://doi.org/10.4049/jimmunol.179.4.2060openalex-snapshot
Cutting Edge: Vitamin D-Mediated Human Antimicrobial Activity against Mycobacterium tuberculosis Is Dependent on the Induction of Cathelicidin
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inferred← citeshttps://doi.org/10.1111/pim.12357openalex-snapshot
Signalling pathways associated with IL ‐6 production and epithelial–mesenchymal transition induction in prostate epithelial cells stimulated with Trichomonas vaginalis
inferred← citeshttps://doi.org/10.1113/jp279423openalex-snapshot
Enhancing responsiveness of human jejunal enteroids to host and microbial stimuli
inferred← citeshttps://doi.org/10.1124/pr.110.002980openalex-snapshot
NADPH Oxidase-Mediated Redox Signaling: Roles in Cellular Stress Response, Stress Tolerance, and Tissue Repair
inferred← citeshttps://doi.org/10.1126/sciimmunol.aat7668openalex-snapshot
Human antimicrobial cytotoxic T lymphocytes, defined by NK receptors and antimicrobial proteins, kill intracellular bacteria
inferred← citeshttps://doi.org/10.1126/scitranslmed.3009546openalex-snapshot
IL-32 is a molecular marker of a host defense network in human tuberculosis
inferred← citeshttps://doi.org/10.1128/iai.00291-21openalex-snapshot
Macrophages in Microbial Pathogenesis: Commonalities of Defense Evasion Mechanisms
inferred← citeshttps://doi.org/10.1128/iai.00344-19openalex-snapshot
Staphylococcus aureus Lipoic Acid Synthesis Limits Macrophage Reactive Oxygen and Nitrogen Species Production To Promote Survival during Infection
inferred← citeshttps://doi.org/10.1128/iai.00471-17openalex-snapshot
Mouse Bone Marrow Sca-1 + CD44 + Mesenchymal Stem Cells Kill Avirulent Mycobacteria but Not Mycobacterium tuberculosis through Modulation of Cathelicidin Expression via the p38 Mitogen-Activated Protein Kinase-Dependent Pathway
inferred← citeshttps://doi.org/10.1128/mbio.00141-11openalex-snapshot
Antimicrobial Actions of Reactive Oxygen Species
inferred← citeshttps://doi.org/10.1128/mbio.01949-19openalex-snapshot
CD157 Confers Host Resistance to Mycobacterium tuberculosis via TLR2-CD157-PKCzeta-Induced Reactive Oxygen Species Production
inferred← citeshttps://doi.org/10.1128/spectrum.05367-22openalex-snapshot
Coevolution of furA -Regulated Hyper-Inflammation and Mycobacterial Resistance to Oxidative Killing through Adaptation to Hydrogen Peroxide
inferred← citeshttps://doi.org/10.1134/s2079086416040095openalex-snapshot
Macrophage and Mycobacterium: The war without beginning or end
inferred← citeshttps://doi.org/10.1139/cjpp-2014-0386openalex-snapshot
Vitamin D: Immuno-modulation and tuberculosis treatment
inferred← citeshttps://doi.org/10.1152/physrev.00034.2023openalex-snapshot
NADPH oxidases: redox regulation of cell homeostasis and disease
inferred← citeshttps://doi.org/10.1155/2017/7949582openalex-snapshot
Central Modulation of Neuroinflammation by Neuropeptides and Energy-Sensing Hormones during Obesity
inferred← citeshttps://doi.org/10.1155/2018/1535194openalex-snapshot
The Biology and Role of Interleukin-32 in Tuberculosis
inferred← citeshttps://doi.org/10.1155/2019/6175804openalex-snapshot
ROS Generation and Antioxidant Defense Systems in Normal and Malignant Cells
inferred← citeshttps://doi.org/10.1155/2020/1269624openalex-snapshot
Roles of Reactive Oxygen Species in Biological Behaviors of Prostate Cancer
inferred← citeshttps://doi.org/10.1155/2021/7086512openalex-snapshot
Oxidative Stress, Neuroinflammation, and NADPH Oxidase: Implications in the Pathogenesis and Treatment of Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1179/1973947815y.0000000043openalex-snapshot
Vitamin D and tuberculosis: a review on a hot topic
inferred← citeshttps://doi.org/10.1186/1546-0096-12-45openalex-snapshot
Immunity against Mycobacterium tuberculosis and the risk of biologic anti-TNF-α reagents
inferred← citeshttps://doi.org/10.1186/s13018-023-04445-6openalex-snapshot
Randomized controlled trial of vitamin d supplementation on toll-like receptor-2 (tlr-2) and toll-like receptor-4 (tlr-4) in tuberculosis spondylitis patients
inferred← citeshttps://doi.org/10.1186/s13578-018-0250-2openalex-snapshot
Phagocytosis influences the intracellular survival of Mycobacterium smegmatis via the endoplasmic reticulum stress response
inferred← citeshttps://doi.org/10.1189/jlb.4ru0416-175rropenalex-snapshot
Interleukin 32: a novel player in the control of infectious diseases
inferred← citeshttps://doi.org/10.1194/jlr.d029546openalex-snapshot
Saturated fatty acids activate TLR-mediated proinflammatory signaling pathways
inferred← citeshttps://doi.org/10.1201/b17311-17openalex-snapshot
Future Strategies and Research Directions in Nutrition–Infection Interactions That Will Enhance Human Health
inferred← citeshttps://doi.org/10.1210/en.2016-1257openalex-snapshot
The NADPH Oxidase Nox2 Mediates Vitamin D-Induced Vascular Regeneration in Male Mice
inferred← citeshttps://doi.org/10.12659/msm.918252openalex-snapshot
Alisol B 23-Acetate Ameliorates Lipopolysaccharide-Induced Cardiac Dysfunction by Suppressing Toll-Like Receptor 4 (TLR4)/NADPH Oxidase 2 (NOX2) Signaling Pathway
inferred← citeshttps://doi.org/10.1371/journal.pone.0036292openalex-snapshot
Activation of an NLRP3 Inflammasome Restricts Mycobacterium kansasii Infection
inferred← citeshttps://doi.org/10.1371/journal.pone.0073333openalex-snapshot
Cholesterol Oxidase Is Indispensable in the Pathogenesis of Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.1371/journal.pone.0147612openalex-snapshot
Uncovering New Pathogen–Host Protein–Protein Interactions by Pairwise Structure Similarity
inferred← citeshttps://doi.org/10.1371/journal.ppat.1000864openalex-snapshot
The Type I NADH Dehydrogenase of Mycobacterium tuberculosis Counters Phagosomal NOX2 Activity to Inhibit TNF-α-Mediated Host Cell Apoptosis
inferred← citeshttps://doi.org/10.1371/journal.ppat.1000930openalex-snapshot
Requirement of NOX2 and Reactive Oxygen Species for Efficient RIG-I-Mediated Antiviral Response through Regulation of MAVS Expression
inferred← citeshttps://doi.org/10.1371/journal.ppat.1001194openalex-snapshot
Potentiation of Epithelial Innate Host Responses by Intercellular Communication
inferred← citeshttps://doi.org/10.1371/journal.ppat.1001230openalex-snapshot
Mycobacterium tuberculosis Eis Regulates Autophagy, Inflammation, and Cell Death through Redox-dependent Signaling
inferred← citeshttps://doi.org/10.1371/journal.ppat.1004617openalex-snapshot
A Rho GDP Dissociation Inhibitor Produced by Apoptotic T-Cells Inhibits Growth of Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.1371/journal.ppat.1005351openalex-snapshot
Mycobacterial Metabolic Syndrome: LprG and Rv1410 Regulate Triacylglyceride Levels, Growth Rate and Virulence in Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.1371/journal.ppat.1008004openalex-snapshot
Fas-associated factor 1 mediates NADPH oxidase-induced reactive oxygen species production and proinflammatory responses in macrophages against Listeria infection
inferred← citeshttps://doi.org/10.1371/journal.ppat.1008354openalex-snapshot
Monocyte metabolic reprogramming promotes pro-inflammatory activity and Staphylococcus aureus biofilm clearance
inferred← citeshttps://doi.org/10.14800/macrophage.756openalex-snapshot
Vitamin D and Macrophage Functions in Tuberculosis
inferred← citeshttps://doi.org/10.15252/embj.2020105543openalex-snapshot
Non‐canonical autophagy functions of ATG16L1 in epithelial cells limit lethal infection by influenza A virus
inferred← citeshttps://doi.org/10.15789/2220-7619-roi-1169openalex-snapshot
Innate immune receptors in development of Mycobacterium tuberculosis infection
inferred← citeshttps://doi.org/10.1586/14789450.2014.971762openalex-snapshot
Improved understanding of pathogenesis from protein interactions inMycobacteriumtuberculosis
inferred← citeshttps://doi.org/10.1586/ecp.11.41openalex-snapshot
Immunomodulation by vitamin D: implications for TB
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4247144/v1openalex-snapshot
Impact of Vitamin D Suplementation in Clinical Outcome at Tuberculosis Spondylitis : Randomized Controlled Trial
inferred← citeshttps://doi.org/10.2174/0929867323666160607222854openalex-snapshot
Human Tuberculosis I. Epidemiology, Diagnosis and Pathogenetic Mechanisms
inferred← citeshttps://doi.org/10.29262/ram.v658i2.859openalex-snapshot
Enfermedad por micobacterias en pacientes con enfermedad granulomatosa crónica
inferred← citeshttps://doi.org/10.3389/fcimb.2012.00145openalex-snapshot
Mycobacterial signaling through toll-like receptors
inferred← citeshttps://doi.org/10.3389/fendo.2022.933965openalex-snapshot
Environmental Triggering of Type 1 Diabetes Autoimmunity
inferred← citeshttps://doi.org/10.3389/fimmu.2017.01906openalex-snapshot
Eat Prey, Live: Dictyostelium discoideum As a Model for Cell-Autonomous Defenses
inferred← citeshttps://doi.org/10.3389/fimmu.2018.00085openalex-snapshot
c-Abl-TWIST1 Epigenetically Dysregulate Inflammatory Responses during Mycobacterial Infection by Co-Regulating Bone Morphogenesis Protein and miR27a
inferred← citeshttps://doi.org/10.3389/fimmu.2019.00065openalex-snapshot
Impact of Vitamin D Supplementation on Influenza Vaccine Response and Immune Functions in Deficient Elderly Persons: A Randomized Placebo-Controlled Trial
inferred← citeshttps://doi.org/10.3389/fimmu.2021.647019openalex-snapshot
Monocytic-Myeloid Derived Suppressor Cells of HIV-Infected Individuals With Viral Suppression Exhibit Suppressed Innate Immunity to Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1660933openalex-snapshot
Mafb deficiency in myeloid cells increases susceptibility to Mycobacterium tuberculosis infection in mice
inferred← citeshttps://doi.org/10.3389/fmicb.2016.00541openalex-snapshot
Insufficient Generation of Mycobactericidal Mediators and Inadequate Level of Phagosomal Maturation Are Related with Susceptibility to Virulent Mycobacterium tuberculosis Infection in Mouse Macrophages
inferred← citeshttps://doi.org/10.3389/fphar.2014.00038openalex-snapshot
The interplay between iron accumulation, mitochondrial dysfunction, and inflammation during the execution step of neurodegenerative disorders
inferred← citeshttps://doi.org/10.3390/cells9030648openalex-snapshot
The Peroxisome Proliferator-Activated Receptor α- Agonist Gemfibrozil Promotes Defense Against Mycobacterium abscessus Infections
inferred← citeshttps://doi.org/10.3390/ijms23094697openalex-snapshot
Urolithin A Inactivation of TLR3/TRIF Signaling to Block the NF-κB/STAT1 Axis Reduces Inflammation and Enhances Antioxidant Defense in Poly(I:C)-Induced RAW264.7 Cells
inferred← citeshttps://doi.org/10.3390/ijms24054546openalex-snapshot
Vitamin D as a Shield against Aging
inferred← citeshttps://doi.org/10.3390/microorganisms12020348openalex-snapshot
Syringaldehyde Exhibits Antibacterial and Antioxidant Activities against Mycobacterium marinum Infection
inferred← citeshttps://doi.org/10.34019/1982-8047.2018.v44.22232openalex-snapshot
Efeitos contrastantes da vitamina D sobre a resposta imune inata e adquirida e seu impacto na recuperação da tuberculose
inferred← citeshttps://doi.org/10.3858/emm.2012.44.2.032openalex-snapshot
Autophagy and bacterial infectious diseases
inferred← citeshttps://doi.org/10.4049/jimmunol.1202574openalex-snapshot
TLR3-Triggered Reactive Oxygen Species Contribute to Inflammatory Responses by Activating Signal Transducer and Activator of Transcription-1
inferred← citeshttps://doi.org/10.4049/jimmunol.1300298openalex-snapshot
Inflammasome-Mediated Secretion of IL-1β in Human Monocytes through TLR2 Activation; Modulation by Dietary Fatty Acids
inferred← citeshttps://doi.org/10.4049/jimmunol.1601651openalex-snapshot
Divergent Functions of TLR2 on Hematopoietic and Nonhematopoietic Cells during Chronic Mycobacterium tuberculosis Infection
inferred← citeshttps://doi.org/10.4110/in.2009.9.5.192openalex-snapshot
Nitric Oxide Synthesis is Modulated by 1,25-Dihydroxyvitamin D3 and Interferon-γ in Human Macrophages after Mycobacterial Infection
inferred← citeshttps://doi.org/10.4110/in.2011.11.5.245openalex-snapshot
Antimicrobial Peptides in Innate Immunity against Mycobacteria
inferred← citeshttps://doi.org/10.4110/in.2014.14.6.307openalex-snapshot
Characterization of Proinflammatory Responses and Innate Signaling Activation in Macrophages Infected withMycobacterium scrofulaceum
inferred← citeshttps://doi.org/10.4110/in.2020.20.e12openalex-snapshot
Vitamin D-Cathelicidin Axis: at the Crossroads between Protective Immunity and Pathological Inflammation during Infection
inferred← citeshttps://doi.org/10.4161/auto.28072openalex-snapshot
The AMPK-PPARGC1A pathway is required for antimicrobial host defense through activation of autophagy
inferred← citeshttps://doi.org/10.4167/jbv.2012.42.2.121openalex-snapshot
Intracellular Signaling Pathways that Regulate Macrophage Chemokine Expression in Response toMycobacterium abscessus
inferred← citeshttps://doi.org/10.5772/30335openalex-snapshot
The Role of Non-Phagocytic Cells in Mycobacterial Infections
inferred← citeshttps://doi.org/10.70675/aa35b30dz2f6fz47cdzb4d6z61363e31b065openalex-snapshot
The mycolic acid dehydratases in mycobacterium abscessus : contribution to pathogenicity and potential drug targets
inferred← citeshttps://doi.org/10.7150/ijbs.10927openalex-snapshot
NOD2 is Involved in the Inflammatory Response after Cerebral Ischemia-Reperfusion Injury and Triggers NADPH Oxidase 2-Derived Reactive Oxygen Species
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