Search results for "Class II"

showing 10 items of 194 documents

BRAF-V600E expression in precursor versus differentiated dendritic cells defines clinically distinct LCH risk groups.

2014

BRAF-V600E expression is identified in hematopoietic progenitor and precursor myeloid dendritic cells in patients with high-risk LCH, and enforced expression of BRAF-V600E in CD11c+ cells recapitulates a high-risk LCH-like phenotype in mice.

MalePathologyendocrine system diseasesCellular differentiationCD34Antigens CD34Mice0302 clinical medicineLangerhans cell histiocytosisBone MarrowRisk FactorsImmunology and Allergyskin and connective tissue diseasesChild0303 health sciencesCell Differentiation3. Good healthHistiocytosismedicine.anatomical_structurePhenotypeTreatment Outcome030220 oncology & carcinogenesisChild PreschoolAntigens Surface2723 Immunology and AllergyFemaleProto-Oncogene Proteins B-rafmedicine.medical_specialtyImmunologyCD11c610 Medicine & healthBiologyArticle03 medical and health sciencesGermline mutationmedicineAnimalsHumansCell LineageGenetic Predisposition to DiseaseLectins C-TypeProgenitor cellneoplasms030304 developmental biology2403 ImmunologyHistocompatibility Antigens Class II302InfantCorrectionDendritic Cellsmedicine.diseaseHematopoietic Stem Cellsdigestive system diseasesCD11c Antigenenzymes and coenzymes (carbohydrates)Histiocytosis Langerhans-CellMannose-Binding Lectins10032 Clinic for Oncology and HematologyMutationBone marrowThe Journal of experimental medicine
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MMP-2, MMP-9, and iNOS Expression in Human Dental Pulp Subjected to Orthodontic Traction

2009

Abstract Objective: To test the hypothesis that some metalloproteinases (MMP-2, MMP-9) and inducible nitric oxide synthetase (iNOS) enzymes in dental pulp samples do not vary when subjected to orthodontic treatment. Materials and Methods: Human dental pulps were taken from male and female patients (N=10; age 10–14 years). A straight wire technique was used with nickel-titanium or steel archwires. The increase of pressure applied on teeth was gradual. Five patients were subjected to premolar extractions after 14 months of treatment and one after 24 months. Samples were Bouin-fixed, paraffin-embedded, and afterwards processed for immunohistochemistry using anti-MMP-2, anti-MMP-9, and anti-iNO…

MaleSettore BIO/17 - IstologiaTime FactorsNitric oxide synthetaseAdolescentTooth Movement TechniquesNitric Oxide Synthase Type IIDentistryOrthodonticsMalocclusion Angle Class IIMatrix metalloproteinaseNickelFemale patientOrthodontic WiresPressurePremolarHumansMedicineBicuspidChildTitaniumOdontoblastsMMP-2Orthodontic wirebusiness.industrymedicine.diseaseImmunohistochemistryBiomechanical PhenomenaDental pulpiNOSmedicine.anatomical_structureMatrix Metalloproteinase 9SteelMatrix Metalloproteinase 2ImmunohistochemistryFemaleStress MechanicalTreatment timeMalocclusionMMP-9businessImmunohistochemistry Dental pulp MMP-2 MMP-9 iNOS.Dental AlloysFollow-Up StudiesThe Angle Orthodontist
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Epitope specificity and Ia restriction of T cell responses to insulin in a system of complementing Ir genes: analysis with primed lymph node T cells …

1983

The antibody response of (H-2b X H-2k)F1 mice to pig insulin (PI) has previously been shown to be under the control of H-2-linked, complementing Ir genes. In addition, this response was reported to depend on the genetic background of the parental strains (Keck, K., Eur. J. Immunol. 1977. 7: 811). Here it is demonstrated that the secondary in vitro response of proliferating T cells shows the same dependence on H-2-linked Ir genes yet an influence of the background genes could not be detected. The complementing genes were mapped to the Kb, I-Ab and Kk, I-Ak regions. For restimulation of F1 T cells by PI, the Ir genes of both parental chromosomes have to be expressed in the same antigen-presen…

MaleT cellT-LymphocytesImmunologyCellGenes MHC Class IIMice Inbred StrainsBiologyLymphocyte ActivationEpitopeCell LineEpitopesMicemedicineImmunology and AllergyAnimalsInsulinGeneGeneticsGenetic Complementation TestHistocompatibility Antigens Class IIT lymphocyteMolecular biologyIn vitroComplementationmedicine.anatomical_structureCell cultureFemaleImmunizationEuropean journal of immunology
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Specificity of H-2-linked Ir gene control in mice: recognition of the core structure A--L in defined sequence analogues of (T,G,)-A--L.

1979

For further characterization of the processes involved in Ir gene control, the specificity of antibodies and the cross-reaction on the level of helper T cells was studied for a series of polypeptide antigens related to poly-L(Tyr,Glu)-poly-DL-Ala–poly-LLys[(T,G)-A–L] but carrying more defined side chains. Helper cell specificity was assayed in an in vitro secondary anti-dinitrophenyl (DNP) response by cross-stimulation of primed T cells with the various polypeptide carriers. It was established that these polypeptides, although showing the same response pattern, were recognized as distinct entities in the immune response by B and T cells. If this common pattern is due to the effect of the sa…

MaleT-LymphocytesImmunologyCellGenes MHC Class IICell SeparationBiologyCross ReactionsAntibodiesMiceImmune systemAntigenmedicineImmunology and AllergyAnimalsBinding siteGeneMice Inbred C3HAlanineImmunogenicityImmune SeraH-2 AntigensMolecular biologyIn vitroMice Inbred C57BLDinitrobenzenesmedicine.anatomical_structurebiology.proteinFemaleAntibodyPeptidesOligopeptidesSpleenEuropean journal of immunology
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Freshly isolated mouse 4F7+ splenic dendritic cells process and present exogenous antigens to T cells.

1994

The antibody 4F7 was reported to recognize an epitope expressed on dendritic cells (DC) from various tissues. To study the ability of splenic 4F7+ dendritic cells to process antigen for presentation to CD4+ T cells, DC were enriched using a separation procedure avoiding overnight culture which could lead to an altered phenotype. These DC were used as antigen-presenting cells (APC) in stimulation cultures of major histocompatibility complex class II-restricted T cells. It was found that they induce antigen-dependent lymphokine production by T cells and therefore could present exogenous antigens. These processing takes place intracellularly, because fixation abrogates presentation to T cells.…

MaleTime FactorsOvalbuminT cellT-LymphocytesImmunologyAntigen presentationAntigen-Presenting CellsCell SeparationIn Vitro TechniquesMicemedicineImmunology and AllergyCytotoxic T cellAnimalsAntigen-presenting cellCells CulturedMice Inbred BALB CCD40biologyAntigen processingHistocompatibility Antigens Class IIAntibodies MonoclonalDendritic cellDendritic CellsNatural killer T cellMolecular biologyCell biologymedicine.anatomical_structureAntigens Surfacebiology.proteinFemalePeptidesSpleenEuropean journal of immunology
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Full length cDNA of rat RT1.DMa and RT1.DMb and expression of RT1.DM genes in dendritic and Langerhans cells.

1997

MHC encoded DM heterodimers and classical MHC class II complexes meet in an endosomal/lysosomal compartment where DM heterodimers support peptide loading of MHC class II. Studies on peptide loading of rat class II and on peptide persistence in cells of the dendritic lineage prompted us to establish full length cDNA clones coding for the subunits alpha and beta of rat DM molecules as well as a mAb directed against the luminal moiety of the beta subunit. Here we describe the establishment of the first full length cDNA clones of rat RT1.DMa and RT1.DMb. The mode of expression of RT1.DM at the transcript level in bone marrow culture-derived dendritic cells, in Langerhans cells and in a number o…

Maleendocrine systemDNA ComplementaryTranscription Geneticmedicine.drug_classClinical BiochemistryBlotting WesternGenes MHC Class IIMolecular Sequence DataGene ExpressionBone Marrow CellsMonoclonal antibodyMajor histocompatibility complexBiochemistryIslets of LangerhansHistocompatibility AntigensGene expressionmedicineAnimalsAmino Acid SequenceCloning MolecularMolecular BiologyPeptide sequenceCells CulturedMHC class IIbiologyBase SequenceChemistryAntibodies MonoclonalDendritic CellsBlotting NorthernMolecular biologyRatsBlotRats Inbred Lewbiology.proteinBeta proteinAntibodyBiological chemistry
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An approach to predictive testing of contact sensitizers in vitro by monitoring their influence on endocytotic mechanisms.

1996

Endocytotic activation of epidermal Langerhans cells (LC) by immunogenic haptens is an early event during development of allergic contact dermatitis. In this work a fast and objective flow-cytometric assay for predictive in vitro testing of contact sensitizers by monitoring their influence on endocytotic mechanisms in murine LC was developed. Epidermal cell suspensions were labelled with a monoclonal antibody directed to MHC class II molecules and pH-sensitive fluorochrome-coupled second-step reagents. For untreated LC a significant quenching of fluorescence intensity by internalization of the MHC-antibody complexes into acidic compartments was noticed. Similar results were obtained in the …

Malemedia_common.quotation_subjectImmunologyImmunologic TestsEndocytosischemistry.chemical_compoundMicemedicineConcanavalin AImmunology and AllergyAnimalsInternalizationAllergic contact dermatitisPhorbol 1213-Dibutyratemedia_commonFluorescent DyesMice Inbred BALB CbiologyHistocompatibility Antigens Class IILectinGeneral Medicinemedicine.diseaseFlow CytometryIn vitroEndocytosischemistryConcanavalin ALangerhans CellsImmunologyDermatitis Allergic ContactPhorbolbiology.proteinIrritantsFemaleHaptenInternational archives of allergy and immunology
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Induction of anamnestic T cell proliferation by antigen-pulsed, bone marrow-derived macrophages.

1981

Bone marrow-derived macrophages (BMM phi) were grown in a liquid culture system in the presence of L cell-conditioned medium as a source of colony-stimulating factor. After a 4-h pulse with antigen, cultured irradiated BMM phi were capable of presenting the antigen to primed T cells as assessed in a T cell proliferation assay. Proliferation was optimal when BMM phi were used between days 5 and 8 of bone marrow cell culture. T cells of Lyt1 and Lyt123 phenotype had to be present at the start of the culture period to yield an optimal response. Conventional antisera and monoclonal antibodies directed against the H-2 I region and the I-A subregion, respectively, proved inhibitory in this system…

Malemedicine.drug_classT cellT-LymphocytesImmunologyGenes MHC Class IIDose-Response Relationship ImmunologicBone Marrow CellsCell CountMice Inbred StrainsBiologyMonoclonal antibodyLymphocyte ActivationAntibodiesEpitopesMiceAntigenmedicineCell AdhesionImmunology and AllergyCytotoxic T cellAnimalsAntigensAntigen-presenting cellCells CulturedImmune response geneMacrophagesHistocompatibility Antigens Class IIMolecular biologymedicine.anatomical_structurePhenotypeImmunologyAntigens SurfaceMyeloid-derived Suppressor CellFemaleBone marrowEuropean journal of immunology
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Study of mandibular growth in patients treated with Frankel s functional regulator (1b)

2012

Objectives: The purpose of this study was to assess mandibular growth in patients with Class II division 1 malocclusions when treated with Fränkel´s functional regulator 1b. Study Design: The treatment group was made up of 43 patients that were divided into two groups: prepubescent (n:28), and pubescent (n:15). The control group included 40 patients who did not receive any kind of treatment and were likewise divided into a prepubescent group (n:19), and a pubescent group (n:21). A computerized cephalometric study was carried out and superimpositions were done in order to assess the antero-posterior, vertical and rotational movements of the mandible. A two-way ANOVA with interaction was done…

Malemedicine.medical_specialtyAdolescentDentistryMandibleMalocclusion Angle Class IIMandibular growthClinical and Experimental DentistrymedicineHumansOrder (group theory)In patientChildGeneral Dentistrybusiness.industryFacial axisMandible:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseOtorhinolaryngologyUNESCO::CIENCIAS MÉDICASOrthopedic surgeryOrthodontic Appliances FunctionalResearch-ArticleFemaleSurgeryAnalysis of varianceMalocclusionbusinessMedicina Oral Patología Oral y Cirugia Bucal
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Non-coordinate synthesis of MHC class II proteins and invariant chains by epidermal Langerhans cells derived from short-term in vitro culture

1994

Epidermal cells (EC) prepared from Lewis rat skin contained 2-3% class II+, LCA+ Langerhans cells (LC). LC enriched from freshly isolated EC suspensions proved highly effective accessory cells when presenting the nominal antigen OVA to an RT1.Bl-restricted ovalbumin (OVA)-specific rat T cell clone. Short-term preculture of the EC resulted in diminished OVA presenting capacity of the LC. Flow cytometry (FCM) analysis of class II and gamma chain expression revealed an up-regulation of class II on the LC's cell surface, consistent with earlier findings in mouse and human. However, while the presence of gamma chains in mouse LC was reported to decline to negligible levels during culture we obse…

Malemedicine.medical_specialtyTime FactorsLangerhans cellCD74OvalbuminT-LymphocytesImmunologyAntigen presentationCD1BiologyFlow cytometryAntigenInternal medicinemedicineAnimalsImmunology and AllergyAntigen-presenting cellCells CulturedAntigen PresentationMHC class IImedicine.diagnostic_testHistocompatibility Antigens Class IIGeneral MedicineFlow CytometryMolecular biologyRatsmedicine.anatomical_structureEndocrinologyRats Inbred LewLangerhans Cellsbiology.proteinFemaleInternational Immunology
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