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Activation of endothelial cells by extracellular vesicles derived from Mycobacterium tuberculosis infected macrophages or mice
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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/pmic.200900840openalex-snapshot
Proteomic analysis identifies highly antigenic proteins in exosomes from M. tuberculosis ‐infected and culture filtrate protein‐treated macrophages
inferredcites →https://doi.org/10.1002/pmic.201300389openalex-snapshot
The roles of extracellular vesicles in cancer biology: Toward the development of novel cancer biomarkers
inferredcites →https://doi.org/10.1016/j.chom.2013.04.015openalex-snapshot
Crosstalk between the Type 1 Interferon and Nuclear Factor Kappa B Pathways Confers Resistance to a Lethal Virus Infection
inferredcites →https://doi.org/10.1016/j.cyto.2007.11.022openalex-snapshot
IL-23 and IL-17 in tuberculosis
inferredcites →https://doi.org/10.1016/j.tube.2014.10.010openalex-snapshot
Deciphering the role of exosomes in tuberculosis
inferredcites →https://doi.org/10.1016/s0166-0934(97)00211-5openalex-snapshot
Endothelial cell monolayers as a model system to investigate dengue shock syndrome
inferredcites →https://doi.org/10.1038/373255a0openalex-snapshot
Differential production of interferon-γ and interleukin-4 in response to Th1- and Th2-stimulating pathogens by γδ T cells in vivo
inferredcites →https://doi.org/10.1038/nrcardio.2017.7openalex-snapshot
Extracellular vesicles in coronary artery disease
inferredcites →https://doi.org/10.1038/nrmicro.2017.60openalex-snapshot
Viral effects on the content and function of extracellular vesicles
inferredcites →https://doi.org/10.1038/srep37975openalex-snapshot
Changes in the Membrane-Associated Proteins of Exosomes Released from Human Macrophages after Mycobacterium tuberculosis Infection
inferredcites →https://doi.org/10.1038/srep43578openalex-snapshot
Exosomes function in antigen presentation during an in vivo Mycobacterium tuberculosis infection
inferredcites →https://doi.org/10.1053/j.gastro.2014.10.040openalex-snapshot
Hepatitis C Virus Infection Induces Autocrine Interferon Signaling by Human Liver Endothelial Cells and Release of Exosomes, Which Inhibits Viral Replication
inferredcites →https://doi.org/10.1074/jbc.m702277200openalex-snapshot
Exosomes Released from Infected Macrophages Contain Mycobacterium avium Glycopeptidolipids and Are Proinflammatory
inferredcites →https://doi.org/10.1093/biosci/biv084openalex-snapshot
Extracellular Vesicles: Composition, Biological Relevance, and Methods of Study
inferredcites →https://doi.org/10.1093/infdis/143.2.266openalex-snapshot
Virus Infection of Endothelial Cells
inferredcites →https://doi.org/10.1093/nar/gki836openalex-snapshot
NF- B controls the global pro-inflammatory response in endothelial cells: evidence for the regulation of a pro-atherogenic program
inferredcites →https://doi.org/10.1111/tmi.12923openalex-snapshot
Human genetic factors in tuberculosis: an update
inferredcites →https://doi.org/10.1126/science.1185449openalex-snapshot
The Population Dynamics and Control of Tuberculosis
inferredcites →https://doi.org/10.1128/jvi.70.4.2208-2214.1996openalex-snapshot
Filovirus-induced endothelial leakage triggered by infected monocytes/macrophages
inferredcites →https://doi.org/10.1146/annurev.pathol.1.110304.100031openalex-snapshot
THE ENDOTHELIUM AS A TARGET FOR INFECTIONS
inferredcites →https://doi.org/10.1152/physrev.1990.70.2.427openalex-snapshot
Cytokines and endothelial cell biology
inferredcites →https://doi.org/10.1155/2013/617809openalex-snapshot
Expression and Function of the Homeostatic Molecule Del-1 in Endothelial Cells and the Periodontal Tissue
inferredcites →https://doi.org/10.1160/th09-03-0186openalex-snapshot
Infection of the endothelium by members of the order Rickettsiales
inferredcites →https://doi.org/10.1161/01.res.47.3.301openalex-snapshot
A proposal linking clearance of circulating lipoproteins to tissue metabolic activity as a basis for understanding atherogenesis.
inferredcites →https://doi.org/10.1172/jci81132openalex-snapshot
Extracellular vesicles and infectious diseases: new complexity to an old story
inferredcites →https://doi.org/10.1182/blood-2013-02-478925openalex-snapshot
Endothelial cells require miR-214 to secrete exosomes that suppress senescence and induce angiogenesis in human and mouse endothelial cells
inferredcites →https://doi.org/10.1182/blood.v91.10.3527openalex-snapshot
Endothelial cells in physiology and in the pathophysiology of vascular disorders.
inferredcites →https://doi.org/10.1186/s12864-015-1511-7openalex-snapshot
NF-κB and IRF pathways: cross-regulation on target genes promoter level
inferredcites →https://doi.org/10.1189/jlb.0904554openalex-snapshot
Active participation of endothelial cells in inflammation
inferredcites →https://doi.org/10.12932/ap0432.32.3.2014openalex-snapshot
Correlation of gammadelta-T-cells, Th17 cells and IL-17 in peripheral blood of patients with allergic rhinitis
inferredcites →https://doi.org/10.1369/jhc.7a7299.2007openalex-snapshot
LPS-induced IL-6, IL-8, VCAM-1, and ICAM-1 Expression in Human Lymphatic Endothelium
inferredcites →https://doi.org/10.1371/journal.pone.0018564openalex-snapshot
Exosomes Released from M.tuberculosis Infected Cells Can Suppress IFN-γ Mediated Activation of Naïve Macrophages
inferredcites →https://doi.org/10.1371/journal.pone.0103811openalex-snapshot
Detection of Mycobacterium tuberculosis Peptides in the Exosomes of Patients with Active and Latent M. tuberculosis Infection Using MRM-MS
inferredcites →https://doi.org/10.1371/journal.pone.0113651openalex-snapshot
Circulating Extracellular Vesicles with Specific Proteome and Liver MicroRNAs Are Potential Biomarkers for Liver Injury in Experimental Fatty Liver Disease
inferredcites →https://doi.org/10.1371/journal.ppat.1003470openalex-snapshot
Endothelial Cell Permeability during Hantavirus Infection Involves Factor XII-Dependent Increased Activation of the Kallikrein-Kinin System
inferredcites →https://doi.org/10.15252/embr.201439363openalex-snapshot
Exosomes and other extracellular vesicles in host–pathogen interactions
inferredcites →https://doi.org/10.1681/asn.2015010074openalex-snapshot
Extracellular Vesicles in Renal Diseases
inferredcites →https://doi.org/10.33393/jcb.2014.2040openalex-snapshot
Extracellular Vesicles in Heart Disease: Excitement for the Future?
inferredcites →https://doi.org/10.3389/fimmu.2016.00592openalex-snapshot
Endothelial Response to Glucocorticoids in Inflammatory Diseases
inferredcites →https://doi.org/10.3390/ijms16034800openalex-snapshot
Extracellular Vesicles in Alzheimer’s Disease: Friends or Foes? Focus on Aβ-Vesicle Interaction
inferredcites →https://doi.org/10.4049/jimmunol.1101377openalex-snapshot
IL-23 Is Required for Long-Term Control of Mycobacterium tuberculosis and B Cell Follicle Formation in the Infected Lung
inferredcites →https://doi.org/10.4049/jimmunol.1103638openalex-snapshot
Exosomes Isolated from Mycobacteria-Infected Mice or Cultured Macrophages Can Recruit and Activate Immune Cells In Vitro and In Vivo
inferredcites →https://doi.org/10.4049/jimmunol.1402894openalex-snapshot
Bacterial Membrane Vesicles Mediate the Release of Mycobacterium tuberculosis Lipoglycans and Lipoproteins from Infected Macrophages
inferredcites →https://doi.org/10.4049/jimmunol.164.9.4853openalex-snapshot
Up-Regulation of VCAM-1 and Differential Expansion of β Integrin-Expressing T Lymphocytes Are Associated with Immunity to Pulmonary Mycobacterium tuberculosis Infection
inferredcites →https://doi.org/10.4103/2045-8932.114760openalex-snapshot
On the Origin of Microparticles: From “Platelet Dust” to Mediators of Intercellular Communication
inferredcites →https://doi.org/10.5527/wjn.v5.i2.125openalex-snapshot
Extracellular vesicles as mediators of vascular inflammation in kidney disease
inferredcites →https://doi.org/10.5772/58390openalex-snapshot
Extracellular Vesicles in Heart Disease: Excitement for the Future ?
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4142354openalex-extracted
Cerebral Venous Sinus Thrombosis and Pulmonary Thromboembolism Complicated by Pulmonary Tuberculosis: A Case Report
inferred← citeshttps://doi.org/10.1002/jcp.30809openalex-snapshot
Extending applications of AFM to fluidic AFM in single living cell studies
inferred← citeshttps://doi.org/10.1007/s00284-026-04978-zopenalex-snapshot
Extracellular Vesicles of Mycobacterium tuberculosis Serve as a Virulence Factor - Current Research Applications
inferred← citeshttps://doi.org/10.1016/b978-0-12-816053-4.00006-7openalex-snapshot
The function and therapeutic use of exosomes in bacterial infections
inferred← citeshttps://doi.org/10.1016/b978-0-443-23891-8.00017-2openalex-snapshot
Theranostic potential of extracellular vesicles released from mycobacteria and mycobacterium-infected host cells
inferred← citeshttps://doi.org/10.1016/b978-0-443-24035-5.00002-5openalex-snapshot
Theragnostic approaches for the management of tuberculosis
inferred← citeshttps://doi.org/10.1016/j.microb.2025.100520openalex-snapshot
Exosomes and Extracellular vesicles, potential tools in the effective management of tuberculosis infection
inferred← citeshttps://doi.org/10.1016/j.molimm.2021.02.010openalex-snapshot
Extracellular vesicles in the context of Mycobacterium tuberculosis infection
inferred← citeshttps://doi.org/10.1016/j.rmcr.2022.101736openalex-snapshot
A Case of Tuberculosis-related Cerebral Venous Sinus Thrombosis and Pulmonary Thromboembolism Successfully Treated with Edoxaban
inferred← citeshttps://doi.org/10.1042/bst20200788openalex-snapshot
The complex, bidirectional role of extracellular vesicles in infection
inferred← citeshttps://doi.org/10.1080/00365521.2020.1759140openalex-snapshot
Extracellular vesicle-associated soluble CD163 and CD206 in patients with acute and chronic inflammatory liver disease
inferred← citeshttps://doi.org/10.1080/19490976.2020.1771985openalex-snapshot
Exosomes transfer miRNAs from cell-to-cell to inhibit autophagy during infection with Crohn’s disease-associated adherent-invasive E. coli
inferred← citeshttps://doi.org/10.1093/infdis/jiad486openalex-snapshot
Extracellular Vesicles From Mycoplasma gallisepticum: Modulators of Macrophage Activation and Virulence
inferred← citeshttps://doi.org/10.1101/2023.04.03.535441openalex-snapshot
Circulating exosomes from Alzheimer’s disease suppress VE-cadherin expression and induce barrier dysfunction in recipient brain microvascular endothelial cell
inferred← citeshttps://doi.org/10.1155/cmi/7976988openalex-snapshot
Regulation of Macrophage Polarization Mediated by Extracellular Vesicle During Bacterial Infection
inferred← citeshttps://doi.org/10.1186/s10020-021-00296-1openalex-snapshot
The emerging role of exosomal miRNAs as a diagnostic and therapeutic biomarker in Mycobacterium tuberculosis infection
inferred← citeshttps://doi.org/10.15252/embr.201846613openalex-snapshot
Extracellular vesicles deliver Mycobacterium RNA to promote host immunity and bacterial killing
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1141503/v1openalex-snapshot
Extending applications of AFM to fluidic AFM in single living cell and extracellular vesicle studies
inferred← citeshttps://doi.org/10.21203/rs.3.rs-7049789/v1openalex-snapshot
Serum Interleukin-4 and Ascitic CD206 Predict Mortality in Acute Cirrhosis Decompensation and Acute-on-Chronic Liver Failure
inferred← citeshttps://doi.org/10.22416/1382-4376-2026-36-1-16-26openalex-snapshot
Ascetic Soluble CD206 and Serum Interleukin-4 Can Predict Mortality in Acute Decompensated and Acute-on-Chronic Liver Failure
inferred← citeshttps://doi.org/10.22514/sv.2022.058openalex-snapshot
New insights in ARDS pathogenesis
inferred← citeshttps://doi.org/10.3233/jad-230347openalex-snapshot
Circulating Exosomes from Alzheimer’s Disease Suppress Vascular Endothelial-Cadherin Expression and Induce Barrier Dysfunction in Recipient Brain Microvascular Endothelial Cell
inferred← citeshttps://doi.org/10.3389/fcimb.2022.912831openalex-snapshot
Extracellular Vesicles in Mycobacteria and Tuberculosis
inferred← citeshttps://doi.org/10.3389/fcimb.2024.1398077openalex-snapshot
Significance of extracellular vesicles in orchestration of immune responses in Mycobacterium tuberculosis infection
inferred← citeshttps://doi.org/10.3389/fimmu.2019.01929openalex-snapshot
Extracellular Vesicles in Mycobacterial Infections: Their Potential as Molecule Transfer Vectors
inferred← citeshttps://doi.org/10.3389/fimmu.2020.01230openalex-snapshot
Trafficking of Mycobacterium tuberculosis Envelope Components and Release Within Extracellular Vesicles: Host-Pathogen Interactions Beyond the Wall
inferred← citeshttps://doi.org/10.3389/fimmu.2021.628973openalex-snapshot
Emerging Role of Exosomes in Tuberculosis: From Immunity Regulations to Vaccine and Immunotherapy
inferred← citeshttps://doi.org/10.3389/fimmu.2022.904679openalex-snapshot
Exosomally Targeting microRNA23a Ameliorates Microvascular Endothelial Barrier Dysfunction Following Rickettsial Infection
inferred← citeshttps://doi.org/10.3389/fimmu.2023.1260859openalex-snapshot
Early innate cell interactions with Mycobacterium tuberculosis in protection and pathology of tuberculosis
inferred← citeshttps://doi.org/10.3389/fmicb.2021.785856openalex-snapshot
Application of Stem Cell-Derived Extracellular Vesicles as an Innovative Theranostics in Microbial Diseases
inferred← citeshttps://doi.org/10.3389/fmicb.2022.1039040openalex-snapshot
Extracellular vesicle-mediated regulation of macrophage polarization in bacterial infections
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1099623openalex-snapshot
Assessment of adaptive immune responses of dairy cows with Burkholderia contaminans-induced mastitis
inferred← citeshttps://doi.org/10.3389/fphys.2021.752287openalex-snapshot
Extracellular Vesicles and Alveolar Epithelial-Capillary Barrier Disruption in Acute Respiratory Distress Syndrome: Pathophysiological Role and Therapeutic Potential
inferred← citeshttps://doi.org/10.3390/cells15181708openalex-snapshot
Hijacking Host Communication: The Central Role of Extracellular Vesicles in Infectious Disease Pathogenesis
inferred← citeshttps://doi.org/10.3390/cells9051175openalex-snapshot
Macrophage Activation Markers, CD163 and CD206, in Acute-on-Chronic Liver Failure
inferred← citeshttps://doi.org/10.3390/ijms242216139openalex-snapshot
Extracellular Vesicles and Their Role in Lung Infections
inferred← citeshttps://doi.org/10.3390/ijms26031155openalex-snapshot
NHERF2 as a Novel Biomarker for Distinguishing MAC Pulmonary Disease from Tuberculosis Based on Proteome Analysis of Serum Extracellular Vesicles
inferred← citeshttps://doi.org/10.3390/microorganisms12122656openalex-snapshot
Host Long Noncoding RNAs as Key Players in Mycobacteria–Host Interactions
inferred← citeshttps://doi.org/10.64898/2025.12.11.693607openalex-snapshot
Bacterial Stimulation Remodels Macrophage Extracellular Vesicle Lipids and Reveals iNOS as an Inflammatory Cargo
inferred← citeshttps://doi.org/10.70675/4ac13bd9zbf56z4ff7za4b8zd2904548ff51openalex-snapshot
Les exosomes, médiateurs fondamentaux de la communication intercellulaire au cours de l'infection par les bactéries AIEC impliquées dans la maladie de Crohn
inferred← citeshttps://doi.org/10.70675/8c2ab1baz3beaz4941zb81dz39aad4dc0e36openalex-snapshot
Vésicules extracellulaires produites par Mycobacterium tuberculosis : composition en lipides et rôle dans les interactions hôte-pathogène
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