Search results for "lymphocyte"

showing 10 items of 2280 documents

β-Catenin in dendritic cells exerts opposite functions in cross-priming and maintenance of CD8+ T cells through regulation of IL-10

2015

Recent studies have demonstrated that β-catenin in DCs serves as a key mediator in promoting both CD4(+) and CD8(+) T-cell tolerance, although how β-catenin exerts its functions remains incompletely understood. Here we report that activation of β-catenin in DCs inhibits cross-priming of CD8(+) T cells by up-regulating mTOR-dependent IL-10, suggesting blocking β-catenin/mTOR/IL-10 signaling as a viable approach to augment CD8(+) T-cell immunity. However, vaccination of DC-β-catenin(-/-) (CD11c-specific deletion of β-catenin) mice surprisingly failed to protect them against tumor challenge. Further studies revealed that DC-β-catenin(-/-) mice were deficient in generating CD8(+) T-cell immunit…

Mice KnockoutImmunity CellularMultidisciplinaryTOR Serine-Threonine KinasesPriming (immunology)Dendritic CellsBiologyBiological SciencesCD8-Positive T-LymphocytesCancer VaccinesCell biologyInterleukin-10Interleukin 10MiceMediatorImmunityCateninNeoplasmsImmunologyCytotoxic T cellAnimalsPI3K/AKT/mTOR pathwayCD8beta Catenin
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Monocyte and lymphocyte apoptosis resistance in acute and chronic brucellosis and its possible implications in clinical management.

2003

This study evaluated the level of susceptibility of monocytes and lymphocytes to spontaneously induced and CH11-induced apoptosis in 16 patients with Brucella infection. The expression of some immunological and apoptotic markers was evaluated. Before therapy, monocytes showed a high level of resistance to spontaneously induced or CH11-induced apoptosis in all patients. In patients with acute infection, this resistance persisted for 10-20 days after treatment was initiated, then decreased; in chronically infected patients, it persisted after 45 days of treatment. Lymphocytes were also more resistant to CH 11-induced apoptosis. The level of activated CD8++ T lymphocytes was high in patients w…

Microbiology (medical)AdultAdolescentLymphocyteApoptosisBrucellaCD8-Positive T-LymphocytesMonocyteBrucellosisMonocytesBrucellosimedicineHumansLymphocytesfas ReceptorChildbiologybusiness.industryMonocyteAntibodies MonoclonalBrucellosisCD8-Positive T-LymphocyteT lymphocytebiology.organism_classificationmedicine.diseaseBrucellaInfectious Diseasesmedicine.anatomical_structureApoptosisChild PreschoolImmunologyAcute DiseaseChronic Diseasebiology.proteinLymphocyteAntibodybusinessCD8Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
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Performance of the QuantiFERON-cytomegalovirus (CMV) assay for detection and estimation of the magnitude and functionality of the CMV-specific gamma …

2012

ABSTRACTThe performance of the QuantiFERON-cytomegalovirus (CMV) assay was compared to that of a flow cytometry intracellular cytokine staining (ICS) method for the detection of CMV-specific gamma interferon (IFN-γ)-producing CD8+T-cell responses in allogeneic stem cell transplant (allo-SCT) recipients and for estimations of their magnitude and functionality. A total of 90 whole-blood specimens from 23 allo-SCT recipients was analyzed by both methods. Overall, the percentage of specimens that yielded concordant results by both methods was 68.8% (κ = 0.691; 95% confidence interval [CI], 0.548 to 0.835), and the sensitivity of the QuantiFERON-CMV assay for the detection of positive IFN-γ T-ce…

Microbiology (medical)AdultMaleClinical BiochemistryImmunologyCongenital cytomegalovirus infectionCytomegalovirusBiologyCD8-Positive T-LymphocytesSensitivity and SpecificityFlow cytometryQuantiFERONGamma interferonDiagnostic Laboratory ImmunologymedicineImmunology and AllergyCytotoxic T cellHumansAgedTransplantationmedicine.diagnostic_testMiddle Agedmedicine.diseaseConfidence intervalImmunologyCytomegalovirus InfectionsFemaleStem cellCD8Interferon-gamma Release TestsStem Cell TransplantationClinical and vaccine immunology : CVI
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Role of bacteria-specific T cells in the immunopathogenesis of reactive arthritis.

1994

Reactive arthritis is a usually self-limited sterile inflammation of joints that follows certain bacterial gastrointestinal or urogenital infections. The immunopathogenesis involves CD4+ T cells, which mediate an antigen-specific TH1 response to bacterial constituents within the joint. Properties of the arthritogenic bacteria and the physicochemical characteristics of the bacterial antigens may contribute to the development of reactive arthritis.

Microbiology (medical)Antigens BacterialImmunity CellularbiologyYersinia InfectionsSterile inflammationT-LymphocytesCD8-Positive T-Lymphocytesbiology.organism_classificationmedicine.diseaseMicrobiologyArthritis ReactiveRatsInfectious DiseasesVirologyImmunologySalmonella InfectionsmedicineAnimalsHumansReactive arthritisBacterial antigenTh1 responseBacteriaTrends in microbiology
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Role of hematopoietic cells in Mycobacterium tuberculosis infection.

2021

Tuberculosis remains one of the most significant causes of mortality worldwide and the current situation shows a re-emergence of TB due to the emergence of new antibiotic-resistant strains and the widespread of disease caused by immunodeficiencies. For these reasons, a big effort is made to improve the therapeutic strategies against Mycobacterium tuberculosis and to perform new therapeutic and diagnostic strategies. This review analyzes the various hematopoietic populations, their role and the different changes they undergo during Mycobacterium tuberculosis infection or disease. We have examined the population of lymphocytes, monocytes, neutrophils, eosinophils and platelets, in orderto und…

Microbiology (medical)Blood PlateletsMyeloidTuberculosisNeutrophilsImmunologyPopulationDiseaseMicrobiologyMonocytesMycobacterium tuberculosismedicineHumansTuberculosisLymphocytesProgenitor celleducationeducation.field_of_studyHematopoietic cellsbiologybusiness.industryMycobacterium tuberculosismedicine.diseasebiology.organism_classificationHematopoietic Stem CellsEosinophilsInfectious Diseasesmedicine.anatomical_structureImmunologyMyeloid cellsBone marrowStem cellbusinessLymphoid cellsTuberculosis (Edinburgh, Scotland)
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In vivo effects of intravascularly applied Escherichia coli hemolysin: dissociation between induction of granulocytopenia and lethality in monkeys.

1993

The effects of intravascular application of endotoxin-depleted Escherichia coli hemolysin (HlyA) was studied in rabbits and monkeys. In rabbits, bolus application of HlyA calculated to effect final blood levels of approximately 2-3 HU/ml (200-300 ng/ml) caused an acute fall of polymorphonuclear blood leukocytes to less than 20% of starting levels within 5 min. Additionally, platelet counts dropped to approximately 30% of starting levels, whereas lymphocyte counts varied considerably and seldom fell to less than 50%. Nine out ten animals that received 2-4 HU/ml toxin died within 90 min post application. These animals presented with signs of acute respiratory failure and post mortem inspectio…

Microbiology (medical)Blood Plateletsmedicine.medical_specialtyPathologyLymphocyteImmunologyBacterial ToxinsSpleenBlood PressurePulmonary EdemaBiologyPulmonary sequestrationLethal Dose 50Hemolysin ProteinsBacterial ProteinsIn vivoInternal medicinemedicineEscherichia coliImmunology and AllergyAnimalsLungLeukopeniaLungDose-Response Relationship DrugPancreatic ElastaseEscherichia coli ProteinsElastaseGeneral Medicinemedicine.diseasePulmonary edemaBlood Cell CountCapillariesMacaca fascicularisEndocrinologymedicine.anatomical_structureInjections Intra-ArterialLiverInjections IntravenousRabbitsmedicine.symptomSpleenAgranulocytosisGranulocytesMedical microbiology and immunology
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Improved assessment of T-cell receptor (TCR) VB repertoire in clinical specimens: combination of TCR-CDR3 spectratyping with flow cytometry-based TCR…

2002

ABSTRACTAntigen-specific T-cell responses may be described by combining three categories: (i) the specificity and effector functions of a T-cell population, (ii) the quantity of T-cell responses (i.e., the number of responding T cells within the CD4/CD8 population), and (iii) the “quality” of T cells (defined by the T-cell receptor [TCR] structure). Several methods to measure T-cell responses are now available including evaluation of T-cell precursors using limiting dilution, the enzyme-linked immunospot assay, ex vivo TCR variable (v)-segment analysis determined by flow cytometry, and TCR-CDR3 length analysis (spectratyping), as well as identification of peptide-specific T cells using majo…

Microbiology (medical)CD4-Positive T-LymphocytesReceptors Antigen T-Cell alpha-betaClinical BiochemistryImmunologyPopulationchemical and pharmacologic phenomenaComplementarity determining regionCD8-Positive T-LymphocytesMajor histocompatibility complexCDR3 SpectratypingFlow cytometryNeoplasmsCellular ImmunologymedicineImmunology and AllergyHumanseducationeducation.field_of_studybiologymedicine.diagnostic_testT-cell receptorhemic and immune systemsFlow CytometryMolecular biologyComplementarity Determining RegionsImmunologybiology.proteinAntibodyCD8Clinical and diagnostic laboratory immunology
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Generation of immune responses against hepatitis C virus by dendritic cells containing NS5 protein-coated microparticles.

2009

ABSTRACTDendritic cells (DCs) internalize and process antigens as well as activate cellular immune responses. The aim of this study was to determine the capacity of DCs that contain antigen-coated magnetic beads to induce immunity against the nonstructural hepatitis C virus (HCV) antigen 5 (NS5). Splenocytes derived from Fms-like tyrosine kinase receptor 3 (Flt3) ligand-pretreated BALB/c mice were incubated with magnetic beads coated with HCV NS5, lipopolysaccharide (LPS), and/or anti-CD40; purified; and used for immunization. Cellular immunity was measured using cytotoxic T-lymphocyte (CTL) and T-cell proliferation assays, intracellular cytokine staining, and a syngeneic tumor challenge us…

Microbiology (medical)Cytotoxicity ImmunologicCellular immunityLipopolysaccharidevirusesT-LymphocytesClinical BiochemistryImmunologychemical and pharmacologic phenomenaHepacivirusBiologyViral Nonstructural Proteinschemistry.chemical_compoundMiceImmune systemAntigenImmunitySplenocyteImmunology and AllergyCytotoxic T cellAnimalsCell ProliferationMice Inbred BALB Cvirus diseasesDendritic CellsCytotoxicity Tests ImmunologicVaccine ResearchMolecular biologyMicrospheresCTL*chemistryCytokinesFemaleClinical and vaccine immunology : CVI
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T lymphocyte-stimulating microbial toxins as ?superantigens?

1991

Infectious pathogens generally have to cope with the host's adaptive immune system, i.e., T and B lymphocytes. Common evasion mechanisms in this complex interaction are antigenic variations, the escape to immunologically priviledged sites or the use of immunosuppressive mechanisms. Many bacteria and other microorganisms eleborate soluble factors or toxins that act suppressively on cells of the immune system, such as pore-forming molecules or proteins that interfere with the function of G proteins. Gram-positive cocci and a mycoplasma have developed an extremely potent mechanism of T cell stimulation by closely mimicking recognition of specific antigen. From the functional similarity to anti…

Microbiology (medical)G proteinT-LymphocytesT cellBacterial ToxinsImmunologyBiologyLymphocyte Activationmedicine.disease_causeMicrobiologyMiceMycoplasmaImmune systemAntigenmedicineSuperantigenAnimalsImmunology and AllergyAntigens BacterialGeneral MedicineMycoplasmaT lymphocyteAcquired immune systemmedicine.anatomical_structureImmunologyMitogensMedical Microbiology and Immunology
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Proliferation and MHC-unrestricted bystander lysis by virus-specific cytotoxic T cells following antigen self-presentation.

1998

Cytotoxic T cells (CTL) not only act as effector cells, but can also serve as antigen-presenting cells (APC) for other CTL due to their expression of major histocompatibility complex (MHC) class I molecules. In the present study we show that independently derived CTL lines (CTLL) with specificity for an L(d)-presented nonapeptide corresponding to amino acids 168-176 of the immediate-early 1 (IE1) protein of murine cytomegalovirus not only lyse syngeneic but also allogeneic target cells, if the peptide is present during the cytolytic assay. Whereas a short peptide pulse is sufficient to render syngeneic cells susceptible to lysis, continued presence of soluble peptide is mandatory for the ly…

Microbiology (medical)ImmunologyAntigen presentationMajor histocompatibility complexLymphocyte ActivationImmediate early proteinImmediate-Early ProteinsMajor Histocompatibility ComplexMiceViral ProteinsAntigenmedicineTumor Cells CulturedImmunology and AllergyCytotoxic T cellAnimalsAntigens ViralB cellCells CulturedAntigen PresentationMice Inbred BALB CbiologyHistocompatibility Antigens Class IGeneral MedicineVirologyMolecular biologyCytolysisCTL*medicine.anatomical_structurebiology.proteinT-Lymphocytes CytotoxicMedical microbiology and immunology
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