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Leishmania donovani Promastigotes Evade the Antimicrobial Activity of Neutrophil Extracellular Traps
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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(2000)30:8<2235::aid-immu2235>3.0.co;2-9openalex-snapshot
Leishmania donovani promastigotes evade the activation of mitogen-activated protein kinases p38, c-Jun N-terminal kinase, and extracellular signal-regulated kinase-1/2 during infection of naive macrophages
inferredcites →https://doi.org/10.1016/j.cub.2005.12.039openalex-snapshot
DNase Expression Allows the Pathogen Group A Streptococcus to Escape Killing in Neutrophil Extracellular Traps
inferredcites →https://doi.org/10.1016/j.cub.2006.01.056openalex-snapshot
An Endonuclease Allows Streptococcus pneumoniae to Escape from Neutrophil Extracellular Traps
inferredcites →https://doi.org/10.1016/j.imbio.2007.11.010openalex-snapshot
Neutrophil granulocytes as host cells and transport vehicles for intracellular pathogens: Apoptosis as infection-promoting factor
inferredcites →https://doi.org/10.1016/j.it.2009.07.011openalex-snapshot
NETs: a new strategy for using old weapons
inferredcites →https://doi.org/10.1016/j.mib.2003.12.004openalex-snapshot
How do neutrophils and pathogens interact?
inferredcites →https://doi.org/10.1016/j.mib.2006.12.005openalex-snapshot
Neutrophil extracellular traps: casting the NET over pathogenesis
inferredcites →https://doi.org/10.1016/j.pt.2009.01.001openalex-snapshot
Leishmania commandeers the host inflammatory response through neutrophils
inferredcites →https://doi.org/10.1016/j.pt.2009.08.003openalex-snapshot
Are neutrophils important host cells for Leishmania parasites?
inferredcites →https://doi.org/10.1016/j.tube.2008.09.009openalex-snapshot
Neutrophil extracellular traps are induced by Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1016/s0021-9258(20)80492-xopenalex-snapshot
Defective galactofuranose addition in lipophosphoglycan biosynthesis in a mutant of Leishmania donovani.
inferredcites →https://doi.org/10.1016/s0166-6851(01)00432-7openalex-snapshot
Targeted gene deletion in Leishmania major identifies leishmanolysin (GP63) as a virulence factor
inferredcites →https://doi.org/10.1016/s0966-842x(03)00075-1openalex-snapshot
Neutrophil granulocytes – Trojan horses for Leishmania major and other intracellular microbes?
inferredcites →https://doi.org/10.1038/nrmicro1710openalex-snapshot
Beneficial suicide: why neutrophils die to make NETs
inferredcites →https://doi.org/10.1042/bj2940305openalex-snapshot
The structure, biosynthesis and function of glycosylated phosphatidylinositols in the parasitic protozoa and higher eukaryotes
inferredcites →https://doi.org/10.1046/j.1462-5822.1999.00002.xopenalex-snapshot
Impaired recruitment of the small GTPase rab7 correlates with the inhibition of phagosome maturation by Leishmania donovani promastigotes
inferredcites →https://doi.org/10.1073/pnas.0900226106openalex-snapshot
Leishmania amazonensis promastigotes induce and are killed by neutrophil extracellular traps
inferredcites →https://doi.org/10.1073/pnas.1530604100openalex-snapshot
The role(s) of lipophosphoglycan (LPG) in the establishment of Leishmania major infections in mammalian hosts
inferredcites →https://doi.org/10.1073/pnas.160257897openalex-snapshot
Lipophosphoglycan is a virulence factor distinct from related glycoconjugates in the protozoan parasite Leishmania major
inferredcites →https://doi.org/10.1073/pnas.97.1.406openalex-snapshot
The role of phosphoglycans in Leishmania –sand fly interactions
inferredcites →https://doi.org/10.1083/jcb.200606027openalex-snapshot
Novel cell death program leads to neutrophil extracellular traps
inferredcites →https://doi.org/10.1084/jem.185.12.2061openalex-snapshot
Inhibition of Phagolysosomal Biogenesis by the Leishmania Lipophosphoglycan
inferredcites →https://doi.org/10.1111/j.1462-5822.2005.00659.xopenalex-snapshot
Neutrophil extracellular traps capture and kill Candida albicans yeast and hyphal forms
inferredcites →https://doi.org/10.1111/j.1462-5822.2006.00758.xopenalex-snapshot
Leishmania donovani lipophosphoglycan blocks NADPH oxidase assembly at the phagosome membrane
inferredcites →https://doi.org/10.1111/j.1462-5822.2006.00857.xopenalex-snapshot
Capsule and d-alanylated lipoteichoic acids protect Streptococcus pneumoniae against neutrophil extracellular traps
inferredcites →https://doi.org/10.1111/j.1462-5822.2007.01018.xopenalex-snapshot
Trafficking of Leishmania donovani promastigotes in non-lytic compartments in neutrophils enables the subsequent transfer of parasites to macrophages
inferredcites →https://doi.org/10.1111/j.1462-5822.2009.01348.xopenalex-snapshot
The impact of vector-mediated neutrophil recruitment on cutaneous leishmaniasis
inferredcites →https://doi.org/10.1111/j.1600-065x.2007.00544.xopenalex-snapshot
To activate or not to activate: distinct strategies used by Helicobacter pylori and Francisella tularensis to modulate the NADPH oxidase and survive in human neutrophils
inferredcites →https://doi.org/10.1111/j.1600-065x.2007.00550.xopenalex-snapshot
How human neutrophils kill and degrade microbes: an integrated view
inferredcites →https://doi.org/10.1126/science.1092385openalex-snapshot
Neutrophil Extracellular Traps Kill Bacteria
inferredcites →https://doi.org/10.1126/science.1159194openalex-snapshot
In Vivo Imaging Reveals an Essential Role for Neutrophils in Leishmaniasis Transmitted by Sand Flies
inferredcites →https://doi.org/10.1126/science.1162914openalex-snapshot
Neutrophil Soldiers or Trojan Horses?
inferredcites →https://doi.org/10.1126/science.7569927openalex-snapshot
A Specialized Pathway Affecting Virulence Glycoconjugates of Leishmania
inferredcites →https://doi.org/10.1128/iai.00051-08openalex-snapshot
β-Hydroxybutyrate Abrogates Formation of Bovine Neutrophil Extracellular Traps and Bactericidal Activity against Mammary PathogenicEscherichia coli
inferredcites →https://doi.org/10.1128/iai.01388-07openalex-snapshot
Neutrophils Contribute to Development of a Protective Immune Response during Onset of Infection withLeishmania donovani
inferredcites →https://doi.org/10.1128/iai.40.1.411-416.1983openalex-snapshot
Interaction of Leishmania donovani Promastigotes with Human Phagocytes
inferredcites →https://doi.org/10.1128/iai.70.2.826-835.2002openalex-snapshot
Intracellular Survival ofLeishmania majorin Neutrophil Granulocytes after Uptake in the Absence of Heat-Labile Serum Factors
inferredcites →https://doi.org/10.1146/annurev.immunol.23.021704.115653openalex-snapshot
HOW NEUTROPHILS KILL MICROBES
inferredcites →https://doi.org/10.1146/annurev.mi.46.100192.000433openalex-snapshot
THE LIPOPHOSPHOGLYCAN OF LEISHMANIA PARASITES
inferredcites →https://doi.org/10.1159/000203699openalex-snapshot
Neutrophil Extracellular Traps: A Strategic Tactic to Defeat Pathogens with Potential Consequences for the Host
inferredcites →https://doi.org/10.1242/jcs.056465openalex-snapshot
An exosome-based secretion pathway is responsible for protein export from Leishmania and communication with macrophages
inferredcites →https://doi.org/10.1371/journal.ppat.1000628openalex-snapshot
The Leishmania donovani Lipophosphoglycan Excludes the Vesicular Proton-ATPase from Phagosomes by Impairing the Recruitment of Synaptotagmin V
inferredcites →https://doi.org/10.1371/journal.ppat.1000639openalex-snapshot
Neutrophil Extracellular Traps Contain Calprotectin, a Cytosolic Protein Complex Involved in Host Defense against Candida albicans
inferredcites →https://doi.org/10.1371/journal.ppat.1000873openalex-snapshot
Production of Extracellular Traps against Aspergillus fumigatus In Vitro and in Infected Lung Tissue Is Dependent on Invading Neutrophils and Influenced by Hydrophobin RodA
inferredcites →https://doi.org/10.4049/jimmunol.127.4.1438openalex-snapshot
Phagocytosis and killing of the protozoan Leishmania donovani by human polymorphonuclear leukocytes.
inferredcites →https://doi.org/10.4049/jimmunol.145.12.4311openalex-snapshot
Serum resistance of metacyclic stage Leishmania major promastigotes is due to release of C5b-9.
inferredcites →https://doi.org/10.4049/jimmunol.163.10.5505openalex-snapshot
Role of Protein Kinase C-α in the Control of Infection by Intracellular Pathogens in Macrophages
inferredcites →https://doi.org/10.4049/jimmunol.173.11.6521openalex-snapshot
Cutting Edge: Neutrophil Granulocyte Serves as a Vector for Leishmania Entry into Macrophages
inferredcites →https://doi.org/10.4049/jimmunol.173.12.7521openalex-snapshot
In Vivo and In Vitro Roles of IL-21 in Inflammation
inferredcites →https://doi.org/10.4049/jimmunol.179.6.3988openalex-snapshot
Neutrophils Activate Macrophages for Intracellular Killing of Leishmania major through Recruitment of TLR4 by Neutrophil Elastase
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Interaction ofLeishmaniaParasites with Host Cells and its Functional Consequences
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Nanobodies for NETosis Tracking and Visualization
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Neutrophils and Visceral Leishmaniasis: Impact on innate immune response and cross‐talks with macrophages and dendritic cells
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Role of Reactive Oxygen Species in Infection by the Intracellular Leishmania Parasites
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Macrophages and neutrophils cooperate in immune responses to Leishmania infection
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Molecular mechanisms regulating NETosis in infection and disease
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The apicomplexan parasite Eimeria arloingi induces caprine neutrophil extracellular traps
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inferred← citeshttps://doi.org/10.1007/s00441-022-03636-7openalex-snapshot
Quantitative phosphoproteomics reveals diverse stimuli activate distinct signaling pathways during neutrophil activation
inferred← citeshttps://doi.org/10.1016/b978-0-12-374279-7.13002-4openalex-snapshot
Subverting Immunity from the Inside: Strategies of Intracellular Survival – Protozoans
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Unique Features of Vector-Transmitted Leishmaniasis and Their Relevance to Disease Transmission and Control
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Arthropod Saliva and Its Role in Pathogen Transmission
inferred← citeshttps://doi.org/10.1016/b978-0-12-816147-0.00006-xopenalex-snapshot
NETosis in other diseases and therapeutic approaches
inferred← citeshttps://doi.org/10.1016/b978-0-12-824465-4.00267-2openalex-snapshot
Subverting Immunity From the Inside: Strategies of Intracellular Survival – Protozoans
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G Protein-Coupled Kinin Receptors and Immunity Against Pathogens
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Glycoconjugates in New World species of Leishmania: Polymorphisms in lipophosphoglycan and glycoinositolphospholipids and interaction with hosts
inferred← citeshttps://doi.org/10.1016/j.biochi.2023.12.003openalex-snapshot
Leishmania donovani mevalonate kinase regulates host actin for inducing phagocytosis
inferred← citeshttps://doi.org/10.1016/j.biochi.2025.01.004openalex-snapshot
Neutrophils and purinergic signaling: Partners in the crime against Leishmania parasites?
inferred← citeshttps://doi.org/10.1016/j.biopha.2021.111671openalex-snapshot
Host immune response against leishmaniasis and parasite persistence strategies: A review and assessment of recent research
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Leishmania exosomes and other virulence factors: Impact on innate immune response and macrophage functions
inferred← citeshttps://doi.org/10.1016/j.cellimm.2016.08.004openalex-snapshot
Leishmania, the phagosome, and host responses: The journey of a parasite
inferred← citeshttps://doi.org/10.1016/j.cellimm.2022.104640openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cellimm.2024.104881openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cytox.2020.100041openalex-snapshot
Macrophages as host, effector and immunoregulatory cells in leishmaniasis: Impact of tissue micro-environment and metabolism
inferred← citeshttps://doi.org/10.1016/j.dci.2013.06.014openalex-snapshot
Shrimp hemocytes release extracellular traps that kill bacteria
inferred← citeshttps://doi.org/10.1016/j.dci.2015.02.002openalex-snapshot
Harbour seal (Phoca vitulina) PMN and monocytes release extracellular traps to capture the apicomplexan parasite Toxoplasma gondii
inferred← citeshttps://doi.org/10.1016/j.dci.2015.05.007openalex-snapshot
NADPH oxidase, MPO, NE, ERK1/2, p38 MAPK and Ca2+ influx are essential for Cryptosporidium parvum-induced NET formation
inferred← citeshttps://doi.org/10.1016/j.dci.2020.103787openalex-snapshot
Fasciola hepatica induces weak NETosis and low production of intra- and extracellular ROS in exposed bovine polymorphonuclear neutrophils
inferred← citeshttps://doi.org/10.1016/j.exppara.2016.05.005openalex-snapshot
Innate immunomodulation to trypanosomatid parasite infections
inferred← citeshttps://doi.org/10.1016/j.exppara.2019.107770openalex-snapshot
Toxoplasma gondii induces extracellular traps release in cat neutrophils
inferred← citeshttps://doi.org/10.1016/j.exppara.2019.107828openalex-snapshot
Newly excysted juveniles of Fasciola gigantica trigger the release of water buffalo neutrophil extracellular traps in vitro
inferred← citeshttps://doi.org/10.1016/j.exppara.2025.108902openalex-snapshot
Molecular host-parasite interaction at the site of vector bite
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Oxidized LDL induced extracellular trap formation in human neutrophils via TLR-PKC-IRAK-MAPK and NADPH-oxidase activation
inferred← citeshttps://doi.org/10.1016/j.fsi.2012.07.020openalex-snapshot
Rac2 expression and its role in neutrophil functions of zebrafish (Danio rerio)
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2020.02.186openalex-snapshot
Functional and structural characterization of an ecotin-like serine protease inhibitor from Trypanosoma cruzi
inferred← citeshttps://doi.org/10.1016/j.intimp.2021.108400openalex-snapshot
Exploring the paradox of defense between host and Leishmania parasite
inferred← citeshttps://doi.org/10.1016/j.intimp.2024.113714openalex-snapshot
Progesterone suppresses rhinovirus-induced airway inflammation by inhibiting neutrophil infiltration and extracellular traps formation
inferred← citeshttps://doi.org/10.1016/j.jaci.2017.07.048openalex-snapshot
Eosinophils release extracellular DNA traps in response to Aspergillus fumigatus
inferred← citeshttps://doi.org/10.1016/j.jbc.2025.108457openalex-snapshot
A major Toxoplasma serine protease inhibitor protects the parasite against gut-derived serine proteases and NETosis damage
inferred← citeshttps://doi.org/10.1016/j.jevs.2018.11.002openalex-snapshot
Extracellular Trap Formation by Donkey Polymorphonuclear Neutrophils Against Toxoplasma gondii
inferred← citeshttps://doi.org/10.1016/j.lfs.2022.121191openalex-snapshot
Eosinophils: Focus on DNA extracellular traps
inferred← citeshttps://doi.org/10.1016/j.lfs.2025.123779openalex-snapshot
Under pressure: Updated insights into the mechanisms of Leishmania's defense in response to oxidative stress
inferred← citeshttps://doi.org/10.1016/j.mam.2025.101419openalex-snapshot
The crosstalk of neutrophil extracellular trap-inflammasome and their roles in disease progression
inferred← citeshttps://doi.org/10.1016/j.medcli.2012.04.022openalex-snapshot
Trampas extracelulares de neutrófilos: un mecanismo de defensa con dos caras
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What’s behind a sand fly bite? The profound effect of sand fly saliva on host hemostasis, inflammation and immunity
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Leishmania virulence factors: focus on the metalloprotease GP63
inferred← citeshttps://doi.org/10.1016/j.micinf.2014.02.012openalex-snapshot
Extracellular traps are associated with human and mouse neutrophil and macrophage mediated killing of larval Strongyloides stercoralis
inferred← citeshttps://doi.org/10.1016/j.micpath.2022.105728openalex-snapshot
Unweaving the NET: Microbial strategies for neutrophil extracellular trap evasion
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Cloning, expression and purification of 3'-nucleotidase/nuclease, an enzyme responsible for the Leishmania escape from neutrophil extracellular traps
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Different Leishmania Species Drive Distinct Neutrophil Functions
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Canine neutrophils activate effector mechanisms in response to Leishmania infantum
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Host liver-derived extracellular vesicles deliver miR-142a-3p induces neutrophil extracellular traps via targeting WASL to block the development of Schistosoma japonicum
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The intriguing host innate immune response: novel anti-parasitic defence by neutrophil extracellular traps
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Insights on adaptive and innate immunity in canine leishmaniosis
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Dying for a cause: NETosis, mechanisms behind an antimicrobial cell death modality
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Neutrophil extracellular traps in immunity and disease
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Leishmaniasis: complexity at the host–pathogen interface
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Balancing the functions of DNA extracellular traps in intracellular parasite infections: implications for host defense, disease pathology and therapy
inferred← citeshttps://doi.org/10.1038/s41598-017-12753-1openalex-snapshot
Role of Mast Cells in clearance of Leishmania through extracellular trap formation
inferred← citeshttps://doi.org/10.1038/s41598-018-36070-3openalex-snapshot
Bovine neutrophils form extracellular traps in response to the gastrointestinal parasite Ostertagia ostertagi
inferred← citeshttps://doi.org/10.1038/s41598-019-42687-9openalex-snapshot
Neutrophil properties in healthy and Leishmania infantum-naturally infected dogs
inferred← citeshttps://doi.org/10.1038/srep08008openalex-snapshot
Capsular polysaccharides from Cryptococcus neoformans modulate production of neutrophil extracellular traps (NETs) by human neutrophils
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Classical ROS-dependent and early/rapid ROS-independent release of Neutrophil Extracellular Traps triggered by Leishmania parasites
inferred← citeshttps://doi.org/10.1042/bsr20180916openalex-snapshot
The state of art of neutrophil extracellular traps in protozoan and helminthic infections
inferred← citeshttps://doi.org/10.1042/bst20200606openalex-snapshot
Understanding the immune responses involved in mediating protection or immunopathology during leishmaniasis
inferred← citeshttps://doi.org/10.1051/parasite/2016006openalex-snapshot
A review of the proposed role of neutrophils in rodent amebic liver abscess models
inferred← citeshttps://doi.org/10.1073/pnas.1414055112openalex-snapshot
SK3 channel and mitochondrial ROS mediate NADPH oxidase-independent NETosis induced by calcium influx
inferred← citeshttps://doi.org/10.1083/jcb.201203170openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/femspd/ftaa060openalex-snapshot
Immune response to Leishmania mexicana: the host–parasite relationship
inferred← citeshttps://doi.org/10.1093/intimm/dxx075openalex-snapshot
How to master the host immune system?Leishmaniaparasites have the solutions!
inferred← citeshttps://doi.org/10.1093/jleuko/qiae196openalex-snapshot
Leishmania amazonensis-derived extracellular vesicles (EVs) induce neutrophil extracellular traps (NETs)
inferred← citeshttps://doi.org/10.1111/cei.12674openalex-snapshot
Permissive and protective roles for neutrophils in leishmaniasis
inferred← citeshttps://doi.org/10.1111/cmi.13195openalex-snapshot
Histoplasma capsulatum ‐induced extracellular DNA trap release in human neutrophils
inferred← citeshttps://doi.org/10.1111/imr.12892openalex-snapshot
Cross talk between intracellular pathogens and cell death
inferred← citeshttps://doi.org/10.1111/j.1365-2249.2011.04518.xopenalex-snapshot
Hypochlorous acid regulates neutrophil extracellular trap release in humans
inferred← citeshttps://doi.org/10.1111/j.1365-3024.2011.01321.xopenalex-snapshot
Contribution of human neutrophils in the development of protective immune response during in vitro Leishmania major infection
inferred← citeshttps://doi.org/10.1111/pim.12332openalex-snapshot
Entamoeba histolytica induces human neutrophils to form NET s
inferred← citeshttps://doi.org/10.1111/pim.12337openalex-snapshot
Neutrophils extracellular traps damage N aegleria fowleri trophozoites opsonized with human I g G
inferred← citeshttps://doi.org/10.1111/pim.70024openalex-snapshot
Redressing the Balance Against B Regulatory Cells: Novel Immunotherapeutic Target in Leishmaniasis
inferred← citeshttps://doi.org/10.1111/sji.13350openalex-snapshot
Activation of neutrophils excels the therapeutic potential of Mycobacterium indicus pranii and heat‐induced promastigotes against antimony‐resistant Leishmania donovani infection
inferred← citeshttps://doi.org/10.1128/iai.01232-13openalex-snapshot
3′-Nucleotidase/Nuclease Activity Allows Leishmania Parasites To Escape Killing by Neutrophil Extracellular Traps
inferred← citeshttps://doi.org/10.1128/iai.05730-11openalex-snapshot
Toxoplasma gondii Triggers Release of Human and Mouse Neutrophil Extracellular Traps
inferred← citeshttps://doi.org/10.1128/mbio.01980-23openalex-snapshot
Mechanisms regulating host cell death during Leishmania infection
inferred← citeshttps://doi.org/10.1146/annurev-cellbio-020520-111016openalex-snapshot
Cellular Mechanisms of NETosis
inferred← citeshttps://doi.org/10.1155/2012/929743openalex-snapshot
ETosis: A Microbicidal Mechanism beyond Cell Death
inferred← citeshttps://doi.org/10.1155/2013/710239openalex-snapshot
Flavonoids and 5-Aminosalicylic Acid Inhibit the Formation of Neutrophil Extracellular Traps
inferred← citeshttps://doi.org/10.1155/2016/5898074openalex-snapshot
Far beyond Phagocytosis: Phagocyte-Derived Extracellular Traps Act Efficiently against Protozoan ParasitesIn VitroandIn Vivo
inferred← citeshttps://doi.org/10.11575/prism/28324openalex-snapshot
The role of extracellular DNA in neutrophil extracellular traps
inferred← citeshttps://doi.org/10.1160/th17-09-0630openalex-snapshot
The Pathophysiological Role of Neutrophil Extracellular Traps in Inflammatory Diseases
inferred← citeshttps://doi.org/10.11606/d.17.2017.tde-06062017-170957openalex-snapshot
Papel da interleucina 6 (IL-6) na resposta inflamatória neutrofílica durante a infecção por Leishmania infantum>
inferred← citeshttps://doi.org/10.1177/1753425918821168openalex-snapshot
Glycoconjugates of Gram-negative bacteria and parasitic protozoa – are they similar in orchestrating the innate immune response?
inferred← citeshttps://doi.org/10.1182/bloodadvances.2020003093openalex-snapshot
Inhibition of NADPH oxidase blocks NETosis and reduces thrombosis in heparin-induced thrombocytopenia
inferred← citeshttps://doi.org/10.1186/s12866-024-03270-zopenalex-snapshot
Neutrophil extracellular traps formation: effect of Leishmania major promastigotes and salivary gland homogenates of Phlebotomus papatasi in human neutrophil culture
inferred← citeshttps://doi.org/10.1186/s13071-015-1219-1openalex-snapshot
Leucocyte-derived extracellular trap formation significantly contributes to Haemonchus contortus larval entrapment
inferred← citeshttps://doi.org/10.1186/s13071-016-1540-3openalex-snapshot
The site of the bite: Leishmania interaction with macrophages, neutrophils and the extracellular matrix in the dermis
inferred← citeshttps://doi.org/10.1186/s13071-017-2222-5openalex-snapshot
Molecular signatures of neutrophil extracellular traps in human visceral leishmaniasis
inferred← citeshttps://doi.org/10.1186/s13071-019-3530-8openalex-snapshot
Role of the lipoxin A4 receptor in the development of neutrophil extracellular traps in Leishmania infantum infection
inferred← citeshttps://doi.org/10.1186/s13071-023-05979-8openalex-snapshot
Trichinella spiralis excretory/secretory products from adult worms inhibit NETosis and regulate the production of cytokines from neutrophils
inferred← citeshttps://doi.org/10.1186/s40064-015-0932-8openalex-snapshot
Prolonged exposure to neutrophil extracellular traps can induce mitochondrial damage in macrophages and dendritic cells
inferred← citeshttps://doi.org/10.1186/s43556-025-00337-9openalex-snapshot
Neutrophil Extracellular Traps (NETs) in health and disease
inferred← citeshttps://doi.org/10.1189/jlb.4a0615-261rropenalex-snapshot
Neutrophil extracellular traps release induced by Leishmania : role of PI3Kγ, ERK, PI3Kσ, PKC, and [Ca2+]
inferred← citeshttps://doi.org/10.1189/jlb.4ri1014-521ropenalex-snapshot
Extracellular traps and macrophages: new roles for the versatile phagocyte
inferred← citeshttps://doi.org/10.1371/journal.pntd.0004037openalex-snapshot
Neutrophil Extracellular Traps Identification in Tegumentary Lesions of Patients with Paracoccidioidomycosis and Different Patterns of NETs Generation In Vitro
inferred← citeshttps://doi.org/10.1371/journal.pntd.0004609openalex-snapshot
Neutrophils Contribute to the Protection Conferred by ArtinM against Intracellular Pathogens: A Study on Leishmania major
inferred← citeshttps://doi.org/10.1371/journal.pntd.0010681openalex-snapshot
Following successful anti-leishmanial treatment, neutrophil counts, CD10 expression and phagocytic capacity remain reduced in visceral leishmaniasis patients co-infected with HIV
inferred← citeshttps://doi.org/10.1371/journal.pntd.0010893openalex-snapshot
Quantitative single-cell analysis of Leishmania major amastigote differentiation demonstrates variably extended expression of the lipophosphoglycan (LPG) virulence factor in different host cell types
inferred← citeshttps://doi.org/10.1371/journal.pone.0090042openalex-snapshot
Escherichia coli and Candida albicans Induced Macrophage Extracellular Trap-Like Structures with Limited Microbicidal Activity
inferred← citeshttps://doi.org/10.1371/journal.pone.0091415openalex-snapshot
Neutrophil Extracellular Traps as Innate Immune Reaction against the Emerging Apicomplexan Parasite Besnoitia besnoiti
inferred← citeshttps://doi.org/10.1371/journal.pone.0133063openalex-snapshot
Are Neutrophil Extracellular Traps Playing a Role in the Parasite Control in Active American Tegumentary Leishmaniasis Lesions?
inferred← citeshttps://doi.org/10.1371/journal.pone.0139569openalex-snapshot
Trypanosoma cruzi and Its Soluble Antigens Induce NET Release by Stimulating Toll-Like Receptors
inferred← citeshttps://doi.org/10.1371/journal.pone.0158979openalex-snapshot
Entamoeba histolytica Trophozoites and Lipopeptidophosphoglycan Trigger Human Neutrophil Extracellular Traps
inferred← citeshttps://doi.org/10.1371/journal.ppat.1003923openalex-snapshot
Lundep, a Sand Fly Salivary Endonuclease Increases Leishmania Parasite Survival in Neutrophils and Inhibits XIIa Contact Activation in Human Plasma
inferred← citeshttps://doi.org/10.1371/journal.ppat.1004929openalex-snapshot
Rapid Sequestration of Leishmania mexicana by Neutrophils Contributes to the Development of Chronic Lesion
inferred← citeshttps://doi.org/10.1371/journal.ppat.1007773openalex-snapshot
Triggering NETosis via protease-activated receptor (PAR)-2 signaling as a mechanism of hijacking neutrophils function for pathogen benefits
inferred← citeshttps://doi.org/10.1371/journal.ppat.1008768openalex-snapshot
Interplay of Trypanosome Lytic Factor and innate immune cells in the resolution of cutaneous Leishmania infection
inferred← citeshttps://doi.org/10.1371/journal.ppat.1012527openalex-snapshot
NLRP1-dependent activation of Gasdermin D in neutrophils controls cutaneous leishmaniasis
inferred← citeshttps://doi.org/10.1371/journal.ppat.1012592openalex-snapshot
Functional plasticity shapes neutrophil response to Leishmania major infection in susceptible and resistant strains of mice
inferred← citeshttps://doi.org/10.1371/journal.ppat.1014197openalex-snapshot
p1/s1, a 3’-nucleotidase/nuclease, allows Leishmania major to circumvent host innate immune response mechanisms
inferred← citeshttps://doi.org/10.14264/uql.2016.1084openalex-snapshot
Immune defence mechanisms of barramundi (Lates calcarifer) peripheral blood against Streptococci
inferred← citeshttps://doi.org/10.1586/14787210.2016.1160779openalex-snapshot
Host resistance to visceral leishmaniasis: prevalence and prevention
inferred← citeshttps://doi.org/10.1590/0037-8682-0506-2025openalex-snapshot
Neutrophil extracellular traps and parasite load are associated with dermal matrix remodeling in Leishmania braziliensis infection
inferred← citeshttps://doi.org/10.1590/1519-6984.252936openalex-snapshot
Quercetin inhibits neutrophil extracellular traps release and their cytotoxic effects on A549 cells, as well the release and enzymatic activity of elastase and myeloperoxidase
inferred← citeshttps://doi.org/10.2174/0115748855295089240322081903openalex-snapshot
Innate Immune Effectors and Leishmania: an Overview of Complexities
inferred← citeshttps://doi.org/10.2217/fmb.14.43openalex-snapshot
Immunity to Visceral Leishmaniasis: Implications for Immunotherapy
inferred← citeshttps://doi.org/10.22456/1679-9216.111869openalex-snapshot
Leukocytes and Albumin in Canine Leishmaniasis
inferred← citeshttps://doi.org/10.31274/etd-180810-1552openalex-snapshot
Rac2 in the zebrafish (Danio rerio) with a focus on neutrophils
inferred← citeshttps://doi.org/10.3389/fcimb.2012.00059openalex-snapshot
The influence of early neutrophil-Leishmania interactions on the host immune response to infection
inferred← citeshttps://doi.org/10.3389/fcimb.2012.00072openalex-snapshot
Impact of Leishmania metalloprotease GP63 on macrophage signaling
inferred← citeshttps://doi.org/10.3389/fcimb.2018.00226openalex-snapshot
Entamoeba histolytica Induce Signaling via Raf/MEK/ERK for Neutrophil Extracellular Trap (NET) Formation
inferred← citeshttps://doi.org/10.3389/fcimb.2019.00153openalex-snapshot
Infection of Human Neutrophils With Leishmania infantum or Leishmania major Strains Triggers Activation and Differential Cytokines Release
inferred← citeshttps://doi.org/10.3389/fcimb.2019.00240openalex-snapshot
Intraspecies Polymorphisms in the Lipophosphoglycan of L. braziliensis Differentially Modulate Macrophage Activation via TLR4
inferred← citeshttps://doi.org/10.3389/fcimb.2021.702125openalex-snapshot
Revisiting the Mechanisms of Immune Evasion Employed by Human Parasites
inferred← citeshttps://doi.org/10.3389/fcimb.2022.788196openalex-snapshot
Leishmania infantum Defective in Lipophosphoglycan Biosynthesis Interferes With Activation of Human Neutrophils
inferred← citeshttps://doi.org/10.3389/fcimb.2022.900895openalex-snapshot
The emerging role of neutrophil extracellular traps in fungal infection
inferred← citeshttps://doi.org/10.3389/fcimb.2024.1364415openalex-snapshot
Editorial: Early events during host cell-pathogen interaction, volume II
inferred← citeshttps://doi.org/10.3389/fimmu.2012.00360openalex-snapshot
Activation of PAD4 in NET formation
inferred← citeshttps://doi.org/10.3389/fimmu.2012.00382openalex-snapshot
Neutrophils cast extracellular traps in response to protozoan parasites
inferred← citeshttps://doi.org/10.3389/fimmu.2012.00420openalex-snapshot
The expanding world of extracellular traps: not only neutrophils but much more
inferred← citeshttps://doi.org/10.3389/fimmu.2013.00001openalex-snapshot
NET balancing: a problem in inflammatory lung diseases
inferred← citeshttps://doi.org/10.3389/fimmu.2014.00193openalex-snapshot
Exploring the Role of Medicinal Plant-Based Immunomodulators for Effective Therapy of Leishmaniasis
inferred← citeshttps://doi.org/10.3389/fimmu.2016.00517openalex-snapshot
Visceral Leishmaniasis Patients Display Altered Composition and Maturity of Neutrophils as well as Impaired Neutrophil Effector Functions
inferred← citeshttps://doi.org/10.3389/fimmu.2017.00523openalex-snapshot
Neutrophil Extracellular Traps Reprogram IL-4/GM-CSF-Induced Monocyte Differentiation to Anti-inflammatory Macrophages
inferred← citeshttps://doi.org/10.3389/fimmu.2017.01437openalex-snapshot
The Equivocal Role of Th17 Cells and Neutrophils on Immunopathogenesis of Leishmaniasis
inferred← citeshttps://doi.org/10.3389/fimmu.2017.01558openalex-snapshot
Survival Mechanisms Used by Some Leishmania Species to Escape Neutrophil Killing
inferred← citeshttps://doi.org/10.3389/fimmu.2017.01849openalex-snapshot
Alkaline pH Promotes NADPH Oxidase-Independent Neutrophil Extracellular Trap Formation: A Matter of Mitochondrial Reactive Oxygen Species Generation and Citrullination and Cleavage of Histone
inferred← citeshttps://doi.org/10.3389/fimmu.2018.02346openalex-snapshot
Allergic Bronchopulmonary Aspergillosis–A Luminal Hypereosinophilic Disease With Extracellular Trap Cell Death
inferred← citeshttps://doi.org/10.3389/fimmu.2018.03040openalex-snapshot
Resistance of Leishmania (Viannia) Panamensis to Meglumine Antimoniate or Miltefosine Modulates Neutrophil Effector Functions
inferred← citeshttps://doi.org/10.3389/fimmu.2019.00959openalex-snapshot
Glycans as Modulators for the Formation and Functional Properties of Neutrophil Extracellular Traps: Used by the Forces of Good and Evil
inferred← citeshttps://doi.org/10.3389/fimmu.2021.649348openalex-snapshot
The Impact of Neutrophil Recruitment to the Skin on the Pathology Induced by Leishmania Infection
inferred← citeshttps://doi.org/10.3389/fimmu.2021.770246openalex-snapshot
The State of Art of Extracellular Traps in Protozoan Infections (Review)
inferred← citeshttps://doi.org/10.3389/fimmu.2022.801182openalex-snapshot
Toll-Like Receptor- and Protein Kinase R-Induced Type I Interferon Sustains Infection of Leishmania donovani in Macrophages
inferred← citeshttps://doi.org/10.3389/fimmu.2022.821007openalex-snapshot
On the Origin of Neutrophil Extracellular Traps in COVID-19
inferred← citeshttps://doi.org/10.3389/fimmu.2022.915392openalex-snapshot
Unveiling Leukocyte Extracellular Traps in Inflammatory Responses of the Central Nervous System
inferred← citeshttps://doi.org/10.3389/fimmu.2022.926446openalex-snapshot
The role of mucosal-associated invariant T cells in visceral leishmaniasis
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1498453openalex-snapshot
Bibliometric analysis of neutrophil extracellular traps induced by protozoan and helminth parasites (2008–2024)
inferred← citeshttps://doi.org/10.3389/fimmu.2026.1873341openalex-snapshot
Leishmania infantum eukaryotic initiation factor 4A modulates in vitro functional activity of human neutrophils
inferred← citeshttps://doi.org/10.3389/fitd.2024.1308585openalex-snapshot
Host skin immunity to arthropod vector bites: from mice to humans
inferred← citeshttps://doi.org/10.3389/fmicb.2016.00402openalex-snapshot
Interaction of Bacterial Exotoxins with Neutrophil Extracellular Traps: Impact for the Infected Host
inferred← citeshttps://doi.org/10.3389/fmicb.2018.00883openalex-snapshot
Leishmania Hijacks Myeloid Cells for Immune Escape
inferred← citeshttps://doi.org/10.3389/fmicb.2018.00966openalex-snapshot
Extracellular Trap Formation in Response to Trypanosoma cruzi Infection in Granulocytes Isolated From Dogs and Common Opossums, Natural Reservoir Hosts
inferred← citeshttps://doi.org/10.3390/cancers14010194openalex-snapshot
Macrophage and Neutrophil Interactions in the Pancreatic Tumor Microenvironment Drive the Pathogenesis of Pancreatic Cancer
inferred← citeshttps://doi.org/10.3390/cells10081891openalex-snapshot
The Immune System Throws Its Traps: Cells and Their Extracellular Traps in Disease and Protection
inferred← citeshttps://doi.org/10.3390/ijms24108975openalex-snapshot
NETosis in Parasitic Infections: A Puzzle That Remains Unsolved
inferred← citeshttps://doi.org/10.3390/microorganisms11071631openalex-snapshot
Is There Any Difference in the In Situ Immune Response in Active Localized Cutaneous Leishmaniasis That Respond Well or Poorly to Meglumine Antimoniate Treatment or Spontaneously Heal?
inferred← citeshttps://doi.org/10.3390/pathogens10111511openalex-snapshot
Tick Immunobiology and Extracellular Traps: An Integrative Vision to Control of Vectors
inferred← citeshttps://doi.org/10.3390/poultry3030024openalex-snapshot
Interaction of Chicken Heterophils and Eimeria tenella Results in Different Phenotypes of Heterophil Extracellular Traps (HETs)
inferred← citeshttps://doi.org/10.3390/tropicalmed8070336openalex-snapshot
Leishmania infantum Axenic Amastigotes Induce Human Neutrophil Extracellular Traps and Resist NET-Mediated Killing
inferred← citeshttps://doi.org/10.3906/vet-2101-53openalex-snapshot
In vitro investigation on extracellular traps formation of cat polymorphonuclear leucocytes against Toxoplasma gondii
inferred← citeshttps://doi.org/10.4049/jimmunol.1103197openalex-snapshot
Galectin-3 Facilitates Neutrophil Recruitment as an Innate Immune Response to a Parasitic Protozoa Cutaneous Infection
inferred← citeshttps://doi.org/10.4049/jimmunol.1400478openalex-snapshot
Immobilized Immune Complexes Induce Neutrophil Extracellular Trap Release by Human Neutrophil Granulocytes via FcγRIIIB and Mac-1
inferred← citeshttps://doi.org/10.4049/jimmunol.2000829openalex-snapshot
Essential Role of Neutrophils in the Protective Immune Response Induced by a Live Attenuated Leishmania Vaccine
inferred← citeshttps://doi.org/10.4155/fmc-2018-0439openalex-snapshot
Host-Directed Therapies for Parasitic Diseases
inferred← citeshttps://doi.org/10.5152/tpd.2018.5952openalex-snapshot
Comparison of Picogreen and Sytox Orange Stains in Quantitative Analysis of Extracellular Trap Formed against Toxoplasma gondii in Polymorphonuclear Leukocytes from Sheep
inferred← citeshttps://doi.org/10.5772/39291openalex-snapshot
Immunology of Leishmaniasis and Future Prospective of Vaccines
inferred← citeshttps://doi.org/10.6084/m9.figshare.24416154openalex-snapshot
Additional file 1 of Trichinella spiralis excretory/secretory products from adult worms inhibit NETosis and regulate the production of cytokines from neutrophils
inferred← citeshttps://doi.org/10.70675/8c1d9716z9dd7z4a34z982az8140c1237ca5openalex-snapshot
Étude des paramètres biologiques de la chimiorésistance aux antimoniés dans un modèle de cycle naturel expérimental de leishmaniose cutanée zoonotique à Leishmania major
inferred← citeshttps://doi.org/10.70675/936aa236zcb6bz44beza64ez2083c046e243openalex-snapshot
Rôle de l'ADN dans l'activation du TLR9 lors de l'infection par Leishmania major : propriétés des séquences génomiques et implication des facteurs protéiques
inferred← citeshttps://doi.org/10.70675/d74489c5z4048z43e4za7ebz0dd46aa98d1bopenalex-snapshot
Modulation fonctionnelle des cellules dendritiques par les « Neutrophil Extracellular Traps »
inferred← citeshttps://doi.org/10.70675/dee93baaz697dz40aaza583z6f750d88fe7fopenalex-snapshot
Dérivés furanosidiques à visée thérapeutique dans la leishmaniose : caractérisation des effets et mode d'action
inferred← citeshttps://doi.org/10.70675/e703b21fzd3dcz4ed4z9a6dzeb6dc7701682openalex-snapshot
Mécanismes impliqués dans l'activité pro- et anti-inflammatoire des "Neutrophil Extracellular Traps" : implications physiopathologiques dans la polyarthrite rhumatoïde
inferred← citeshttps://doi.org/10.7936/k79w0ch8openalex-snapshot
Leishmania persistence and host cell interactions
inferred← citeshttps://doi.org/10.82308/19433openalex-snapshot
Parasite and host determinants of visceral leishmaniasis
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