Search results for "immunotoxicology"

showing 4 items of 4 documents

Immuno-toxicological Evaluation of the Adjuvant Formulations for Experimental Anti-meningococcal Vaccines without Aluminium Hydroxide

2019

International audience; The proteoliposomes and cochleates are used as adjuvants for vaccines since they are potent immune stimulators. However, the hyper stimulation of the immune system provoked by adjuvants can cause immunetoxicological side effects. The present study was carried out to evaluate the toxic and immuno-toxicological effects of new adjuvants for anti-meningococci vaccines based on neo-proteoliposomes (nPL) and neocochleates (nCh), in Balb/c mice that were administered doses of 15 µg each, over periods of 14 days through intramuscular route and three inoculations with the same doses through intranasal route, every 7 days. The Scanning and Transmission Electron Microscopy show…

Materials Science (miscellaneous)medicine.medical_treatmentcochleatesSpleenStimulationMeningococcal vaccineImmunotoxicologyPharmacology010402 general chemistry01 natural sciencesGeneral Biochemistry Genetics and Molecular BiologyImmune systemproteoliposomesMaterials ChemistryMedicineGeneral Pharmacology Toxicology and Pharmaceuticsbusiness.industryProcess Chemistry and TechnologyGeneral EngineeringGeneral ChemistryGeneral Medicine0104 chemical sciences3. Good healthimmunotoxicologymedicine.anatomical_structureadjuvantsToxicity[SDE]Environmental SciencesNasal administrationnanoparticlesbusinessAdjuvant
researchProduct

Aroclor 1254 inhibits the chemiluminescence response of peritoneal cavity cells from sharpsnout sea bream (Diplodus puntazzo)

2014

Chronic exposure to polychlorinated biphenyls (PCBs) affect the immune system of fish and could lead to a decreased disease resistance. The effects of Aroclor 1254, PCB mixtures, on the Diplodus puntazzo innate immunity were examined by assaying the zymosan stimulated chemiluminescence response (CL) of peritoneal cavity cells (PCCs) at various times (1, 24, 48 h and 1-4 weeks) from intraperitoneal injection of the xenobiotic (1 mg kg(-1) body weight). Controls were performed by assaying cells from medium-treated fish. Since the kinetic of the chemiluminescence response showed the highest peak at 25 min after the zymosan stimulation of the cells, the values found at that time were considered…

Respiratory burstmedicine.medical_specialtyPhagocytemedicine.medical_treatmentIntraperitoneal injectionSettore BIO/05 - ZoologiaImmunotoxicologyAquatic ScienceBiologychemistry.chemical_compoundPeritoneal cavityPhagocytosisInternal medicineAroclor 1254medicineAnimalsEnvironmental ChemistryPeritoneal CavityPhagocytesInnate immune systemDiplodus puntazzoZymosanGeneral MedicineChlorodiphenyl (54% Chlorine)Peritoneal cavity cellsImmunity InnatePerciformesRespiratory burstEndocrinologymedicine.anatomical_structurechemistryLuminescent MeasurementsChemiluminescence responseXenobioticInjections IntraperitonealDiplodus puntazzo; Aroclor 1254; Chemiluminescence response; Respiratory burst; Peritoneal cavity cells
researchProduct

Transcriptomic study of the toxic mechanism triggered by beauvericin in Jurkat cells

2018

Beauvericin (BEA), an ionophoric cyclic hexadepsipeptide mycotoxin, is able to increase oxidative stress by altering membrane ion permeability and uncoupling oxidative phosphorylation. A toxicogenomic study was performed to investigate gene expression changes triggered by BEA exposure (1.5, 3 and 5 mu M; 24 h) in Jurkat cells through RNA-sequencing and differential gene expression analysis. Perturbed gene expression was observed in a concentration dependent manner, with 43 differentially expressed genes (DEGs) overlapped in the three studied concentrations. Gene ontology (GO) analysis showed several biological processes related to electron transport chain, oxidative phosphorylation, and cel…

0301 basic medicineProgrammed cell deathCYTOCHROME-C RELEASEBCL-2 FAMILYCell Membrane PermeabilityRespiratory chainCell Culture TechniquesCASPASE-3 ACTIVATIONApoptosisOxidative phosphorylationCHO-K1 CELLSToxicologyJurkat cellsOxidative PhosphorylationElectron Transport03 medical and health sciencesJurkat CellsFUSARIUM MYCOTOXINSImmunotoxicologyDepsipeptidesHumansREAL-TIME PCROXIDATIVE STRESSTranscriptomicsCaspaseINDUCED APOPTOSISLEUKEMIA-CELLS030102 biochemistry & molecular biologybiologyDose-Response Relationship DrugChemistryJurkatGene Expression ProfilingBcl-2 familyDEATHGeneral MedicineBeauvericinToxicogenomicsCell biologyGene expression profiling030104 developmental biologyMitochondrial respiratory chainGene Ontologybiology.proteinRNA-seqTranscriptomeToxicology Letters
researchProduct

In vitro effects of methylmercury on ascidian (Styela plicata) immunocyte responses

2007

This study shows that high methylmercury concentrations are cytotoxic for Styela plicata hemocytes, whereas sublethal concentrations affect immunocyte responses. Moreover, hemocytes exposed to the xenobiotic present a significantly enhanced phenoloxidase activity as revealed in the hemocyte lysate supernatant compared with the control. Although the cytotoxic activity of S. plicata hemocytes toward rabbit erythrocytes is a PO-dependent cell-target reaction due to quinone products, it was significantly decreased by suitable methylmercury concentrations in the medium. The same xenobiotic concentrations decreased the hemocyte phagocytic activity toward yeast. In both the responses cell-target c…

Ascidian Galectin Endostyle Inflammation Ciona intestinalisbiologyChemistryPhagocytosisGeneral ChemistryImmunotoxicologybiology.organism_classificationMolecular biologyIn vitroTunicateInorganic ChemistryToxicologychemistry.chemical_compoundStyela plicataCytotoxic T cellXenobioticMethylmercury
researchProduct