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Anisakidae parasitism activated immune response and induced liver fibrosis in wild anadromous Coilia nasus

https://doi.org/10.1111/jfb.15027
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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/tox.20262openalex-snapshot
Bioaccumulation and ROS generation in liver of freshwater fish, goldfish Carassius auratus under HC Orange No. 1 exposure
inferredcites →https://doi.org/10.1016/0014-4894(86)90012-3openalex-snapshot
Anisakis simplex: Larval excretory secretory protein production and cytostatic action in mammalian cell cultures
inferredcites →https://doi.org/10.1016/0020-7519(95)00111-5openalex-snapshot
In vitro study on the effect of larval excretory/secretory products and crude extracts from Anisakis simplex on blood coagulation
inferredcites →https://doi.org/10.1016/bs.apar.2017.12.001openalex-snapshot
Molecular Epidemiology of Anisakis and Anisakiasis: An Ecological and Evolutionary Road Map
inferredcites →https://doi.org/10.1016/j.aquatox.2018.05.001openalex-snapshot
An in vivo analysis of Cr6+ induced biochemical, genotoxicological and transcriptional profiling of genes related to oxidative stress, DNA damage and apoptosis in liver of fish, Channa punctatus (Bloch, 1793)
inferredcites →https://doi.org/10.1016/j.biocel.2014.07.010openalex-snapshot
Delineating the roles of neutrophils and macrophages in zebrafish regeneration models
inferredcites →https://doi.org/10.1016/j.cbpc.2007.01.002openalex-snapshot
Bioaccumulation and ROS generation in liver of Carassius auratus, exposed to phenanthrene
inferredcites →https://doi.org/10.1016/j.cbpc.2019.108640openalex-snapshot
Induction of time- and dose-dependent oxidative stress of triazophos to brain and liver in zebrafish (Danio rerio)
inferredcites →https://doi.org/10.1016/j.cld.2013.09.010openalex-snapshot
The Impact of Obesity on Liver Histology
inferredcites →https://doi.org/10.1016/j.dci.2011.11.009openalex-snapshot
Mucosal immunoglobulins and B cells of teleost fish
inferredcites →https://doi.org/10.1016/j.dci.2016.06.025openalex-snapshot
The teleost head kidney: Integrating thyroid and immune signalling
inferredcites →https://doi.org/10.1016/j.dci.2020.103886openalex-snapshot
Innate cell-mediated cytotoxicity of CD8+ T cells against the protozoan parasite Ichthyophthirius multifiliis in the ginbuna crucian carp, Carassius auratus langsdorfii
inferredcites →https://doi.org/10.1016/j.exppara.2018.10.001openalex-snapshot
Immunomodulatory effects of Trichinella spiralis excretory-secretory antigens on macrophages
inferredcites →https://doi.org/10.1016/j.fsi.2013.06.007openalex-snapshot
Effects of excretory/secretory products from Anisakis simplex (Nematoda) on immune gene expression in rainbow trout (Oncorhynchus mykiss)
inferredcites →https://doi.org/10.1016/j.fsi.2014.11.019openalex-snapshot
Production of inflammatory mediators and extracellular traps by carp macrophages and neutrophils in response to lipopolysaccharide and/or interferon-γ2
inferredcites →https://doi.org/10.1016/j.fsi.2018.10.084openalex-snapshot
Antioxidative, inflammatory and immune responses in hydrogen peroxide-induced liver injury of tilapia (GIFT, Oreochromis niloticus)
inferredcites →https://doi.org/10.1016/j.fsi.2018.11.039openalex-snapshot
Role of teleost B cells in viral immunity
inferredcites →https://doi.org/10.1016/j.fsi.2018.12.077openalex-snapshot
Transcriptome and metabolome analyses of Coilia nasus in response to Anisakidae parasite infection
inferredcites →https://doi.org/10.1016/j.ijpara.2020.04.007openalex-snapshot
Why ignoring parasites in fish ecology is a mistake
inferredcites →https://doi.org/10.1016/j.ijppaw.2019.04.007openalex-snapshot
Anisakis Nematodes in Fish and Shellfish- from infection to allergies
inferredcites →https://doi.org/10.1016/j.immuni.2016.02.015openalex-snapshot
Macrophages in Tissue Repair, Regeneration, and Fibrosis
inferredcites →https://doi.org/10.1016/j.jhep.2013.03.033openalex-snapshot
Decoding cell death signals in liver inflammation
inferredcites →https://doi.org/10.1016/j.margen.2015.02.005openalex-snapshot
Ovary transcriptome profiling of Coilia nasus during spawning migration stages by Illumina sequencing
inferredcites →https://doi.org/10.1016/j.mcp.2014.02.003openalex-snapshot
Foodborne anisakiasis and allergy
inferredcites →https://doi.org/10.1016/j.molimm.2015.09.026openalex-snapshot
Polarization of immune responses in fish: The ‘macrophages first’ point of view
inferredcites →https://doi.org/10.1016/j.rvsc.2020.08.003openalex-snapshot
Anisakiasis and Anisakis: An underdiagnosed emerging disease and its main etiological agents
inferredcites →https://doi.org/10.1016/j.vetimm.2008.07.013openalex-snapshot
Fish immunity and parasite infections: from innate immunity to immunoprophylactic prospects
inferredcites →https://doi.org/10.1016/s0065-308x(08)60573-4openalex-snapshot
Anisakis and Anisakiasis
inferredcites →https://doi.org/10.1016/s0145-305x(01)00037-4openalex-snapshot
Antimicrobial mechanisms of fish phagocytes and their role in host defense
inferredcites →https://doi.org/10.1016/s0168-8278(02)00429-4openalex-snapshot
Liver fibrosis – from bench to bedside
inferredcites →https://doi.org/10.1016/s0301-0546(03)79211-8openalex-snapshot
Anisakis y anisakiosis
inferredcites →https://doi.org/10.1016/s1665-2681(19)32127-1openalex-snapshot
Liver fibrosis and inflammation. A review
inferredcites →https://doi.org/10.1017/erm.2016.14openalex-snapshot
Molecular mechanism of hepatic steatosis: pathophysiological role of autophagy
inferredcites →https://doi.org/10.1038/ni.2549openalex-snapshot
Fishing for mammalian paradigms in the teleost immune system
inferredcites →https://doi.org/10.1038/s41467-019-09046-8openalex-snapshot
Neutrophils promote the development of reparative macrophages mediated by ROS to orchestrate liver repair
inferredcites →https://doi.org/10.1038/s41575-020-00372-7openalex-snapshot
Molecular and cellular mechanisms of liver fibrosis and its regression
inferredcites →https://doi.org/10.1038/s41598-018-34174-4openalex-snapshot
Analysis of the Trichuris suis excretory/secretory proteins as a function of life cycle stage and their immunomodulatory properties
inferredcites →https://doi.org/10.1038/srep31835openalex-snapshot
Integrated application of transcriptomics and metabolomics yields insights into population-asynchronous ovary development in Coilia nasus
inferredcites →https://doi.org/10.1042/cs20170220openalex-snapshot
A past and present overview of macrophage metabolism and functional outcomes
inferredcites →https://doi.org/10.1051/medsci/2009254405openalex-snapshot
Arche de Noé immunologique
inferredcites →https://doi.org/10.1056/nejmra052723openalex-snapshot
The Many Roles of Chemokines and Chemokine Receptors in Inflammation
inferredcites →https://doi.org/10.1074/jbc.m112.349126openalex-snapshot
Live Imaging Reveals Differing Roles of Macrophages and Neutrophils during Zebrafish Tail Fin Regeneration
inferredcites →https://doi.org/10.1093/ilar.38.1.41openalex-snapshot
The 1996 Guide for the Care and Use of Laboratory Animals
inferredcites →https://doi.org/10.1111/j.1365-2761.1982.tb00497.xopenalex-snapshot
The histopathology of larval anisakid nematode infections in the liver of whiting, Merlangius merlangus (L.), with some observations on blood leucocytes of the fish
inferredcites →https://doi.org/10.1111/j.1751-0813.2001.tb10753.xopenalex-snapshot
Immune responses of teleost fish
inferredcites →https://doi.org/10.1111/jfb.14136openalex-snapshot
Digestive enzyme activity of the Japanese grenadier anchovyCoilia nasusduring spawning migration: influence of the migration distance and the water temperature
inferredcites →https://doi.org/10.1111/jfd.12049openalex-snapshot
Cell types and structures involved in tench, Tinca tinca (L.), defence mechanisms against a systemic digenean infection
inferredcites →https://doi.org/10.1111/jfd.12641openalex-snapshot
Liver of the fishGymnotus inaequilabiatusand nematode larvae infection: Histochemical features and expression of proliferative cell nuclear antigen
inferredcites →https://doi.org/10.1111/liv.14091openalex-snapshot
Ischaemia reperfusion injury in liver transplantation: Cellular and molecular mechanisms
inferredcites →https://doi.org/10.1111/pim.12456openalex-snapshot
Effect of ES products from Anisakis (Nematoda: Anisakidae) on experimentally induced colitis in adult zebrafish
inferredcites →https://doi.org/10.1111/pim.12675openalex-snapshot
Immune response to Ichthyophthirius multifiliis and role of IgT
inferredcites →https://doi.org/10.1172/jci88881openalex-snapshot
Liver inflammation and fibrosis
inferredcites →https://doi.org/10.1186/1471-2164-15-558openalex-snapshot
Transcriptome analysis gene expression in the liver of Coilia nasus during the stress response
inferredcites →https://doi.org/10.1186/s12929-015-0206-3openalex-snapshot
Caffeine reduces hepatic lipid accumulation through regulation of lipogenesis and ER stress in zebrafish larvae
inferredcites →https://doi.org/10.1186/s13028-017-0310-3openalex-snapshot
Excretory/secretory products of anisakid nematodes: biological and pathological roles
inferredcites →https://doi.org/10.1186/s13071-016-1772-2openalex-snapshot
Nematode infection in liver of the fish Gymnotus inaequilabiatus (Gymnotiformes: Gymnotidae) from the Pantanal Region in Brazil: pathobiology and inflammatory response
inferredcites →https://doi.org/10.1186/s13071-018-3007-1openalex-snapshot
Hints on T cell responses in a fish-parasite model: Enteromyxum leei induces differential expression of T cell signature molecules depending on the organ and the infection status
inferredcites →https://doi.org/10.1186/s13071-019-3593-6openalex-snapshot
Characterisation of a niche-specific excretory–secretory peroxiredoxin from the parasitic nematode Teladorsagia circumcincta
inferredcites →https://doi.org/10.1186/s13567-018-0620-0openalex-snapshot
CD4: a vital player in the teleost fish immune system
inferredcites →https://doi.org/10.1189/jlb.1012544openalex-snapshot
ROS production in phagocytes: why, when, and where?
inferredcites →https://doi.org/10.1189/jlb.3hi0215-064ropenalex-snapshot
Neutrophil contributions to the induction and regulation of the acute inflammatory response in teleost fish
inferredcites →https://doi.org/10.1371/journal.pone.0047070openalex-snapshot
Fish and Mammalian Phagocytes Differentially Regulate Pro-Inflammatory and Homeostatic Responses In Vivo
inferredcites →https://doi.org/10.1371/journal.pone.0103832openalex-snapshot
De Novo Transcriptomes of Olfactory Epithelium Reveal the Genes and Pathways for Spawning Migration in Japanese Grenadier Anchovy (Coilia nasus)
inferredcites →https://doi.org/10.1371/journal.pone.0181277openalex-snapshot
Immunomodulatory effects of excretory/secretory compounds from Contracaecum osculatum larvae in a zebrafish inflammation model
inferredcites →https://doi.org/10.1371/journal.pone.0222339openalex-snapshot
Protective effect of lactobacillus plantarum on alcoholic liver injury and regulating of keap-Nrf2-ARE signaling pathway in zebrafish larvae
inferredcites →https://doi.org/10.1590/s1984-29612019080openalex-snapshot
Immune response of teleost fish to helminth parasite infection
inferredcites →https://doi.org/10.1645/12-144.1openalex-snapshot
Population Genetic Structure of the AcanthocephalanAcanthosentis cheniin Anadromous, Freshwater, and Landlocked Stocks of Its Fish Host,Coilia nasus
inferredcites →https://doi.org/10.1645/ge-2194.1openalex-snapshot
Anisakid Larvae in Atlantic Salmon (Salmo salar L.) Grilse and Post-Smolts: Molecular Identification and Histopathology
inferredcites →https://doi.org/10.1645/ge-2621.1openalex-snapshot
Seasonal Occurrence of Helminths in the Anadromous Fish Coilia nasus (Engraulidae): Parasite Indicators of Fish Migratory Movements
inferredcites →https://doi.org/10.24272/j.issn.2095-8137.2019.035openalex-snapshot
Specific function and modulation of teleost monocytes/macrophages: polarization and phagocytosis
inferredcites →https://doi.org/10.2741/a171openalex-snapshot
Cytokines in acute and chronic inflammation
inferredcites →https://doi.org/10.3354/dao034027openalex-snapshot
Neutrophil and macrophage responses to inflammation in the peritoneal cavity of rainbow trout Oncorhynchus mykiss. A light and electron microscopic cytochemical study
inferredcites →https://doi.org/10.3389/fimmu.2020.00152openalex-snapshot
Fish Macrophages Show Distinct Metabolic Signatures Upon Polarization
inferredcites →https://doi.org/10.3389/fimmu.2020.01093openalex-snapshot
Back From the Brink: Alterations in B and T Cell Responses Modulate Recovery of Rainbow Trout From Chronic Immunopathological Tetracapsuloides bryosalmonae Infection
inferredcites →https://doi.org/10.3389/fimmu.2020.567941openalex-snapshot
Immunoglobulins, Mucosal Immunity and Vaccination in Teleost Fish
inferredcites →https://doi.org/10.3390/antiox9121279openalex-snapshot
Molecular Mechanisms That Link Oxidative Stress, Inflammation, and Fibrosis in the Liver
inferredcites →https://doi.org/10.3390/biology4040881openalex-snapshot
Biology of Bony Fish Macrophages
inferredcites →https://doi.org/10.3390/ijms20071723openalex-snapshot
The Role of Fibrosis and Liver-Associated Fibroblasts in the Pathogenesis of Hepatocellular Carcinoma
inferredcites →https://doi.org/10.3748/wjg.v22.i48.10512openalex-snapshot
Liver fibrosis and hepatic stellate cells: Etiology, pathological hallmarks and therapeutic targets
inferredcites →https://doi.org/10.5152/tjg.2018.17330openalex-snapshot
Liver fibrosis
inferredcites →https://doi.org/10.5152/tjg.2019.17339openalex-snapshot
Diagnostic accuracy of glycoproteins in the assessment of liver fibrosis: A comparison between laminin, fibronectin, and hyaluronic acid

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.4670192openalex-extracted
inferred← citeshttps://doi.org/10.1007/s00436-025-08565-2openalex-snapshot
Cellular responses in rainbow trout Oncorhynchus mykiss to experimental Anisakis simplex infection
inferred← citeshttps://doi.org/10.1016/j.cbd.2024.101261openalex-snapshot
Hepatic immune response of Coilia nasus infected with Anisakidae during ovarian development
inferred← citeshttps://doi.org/10.1017/s0022149x26101497openalex-snapshot
Influence of crude extracts from different thermally treated Hysterothylacium thalassini L3 larvae on liver pathology and immune responses in C57BL/6 mice
inferred← citeshttps://doi.org/10.1017/s003118202510053xopenalex-snapshot
A portrait of 2 nematodes in liver of their paratenic fish hosts, illustrating different immunological approaches
inferred← citeshttps://doi.org/10.3390/d16030167openalex-snapshot
Ascaridoid Nematodes Infection in Anadromous Fish Coilia nasus from Yangtze River
inferred← citeshttps://doi.org/10.3390/fishes11080453openalex-snapshot
Innate Immune Encapsulation Allows Gonadal Tolerance to Anisakis simplex (s.s.) Infection in Atlantic mackerel (Scomber scombrus)
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