Search results for "immunofluorescence"

showing 10 items of 112 documents

Neuronal and BBB damage induced by sera from patients with secondary progressive multiple sclerosis.

2009

An important component of the pathogenic process of multiple sclerosis (MS) is the blood-brain barrier (BBB) damage. We recently set an in vitro model of BBB, based on a three-cell-type co-culture system, in which rat neurons and astrocytes synergistically induce brain capillary endothelial cells to form a monolayer with permeability properties resembling those of the physiological BBB. Herein we report that the serum from patients with secondary progressive multiple sclerosis (SPMS) has a damaging effect on isolated neurons. This finding suggests that neuronal damaging in MS could be a primary event and not only secondary to myelin damage, as generally assumed. SPMS serum affects the perme…

Pathologymedicine.medical_specialtyProgrammed cell deathBlotting WesternBiologyImmunofluorescenceOccludinModels BiologicalMyelinWestern blotOccludinGeneticsmedicineElectric ImpedanceAnimalsmultiple sclerosis brain cell cultures in vitro models of blood-brain barrier neuronal cell death transendothelial electrical resistanceMicroscopy Phase-ContrastRats WistarCells CulturedNeuronsmedicine.diagnostic_testTight junctionCell DeathMultiple sclerosisMembrane ProteinsGeneral MedicineMultiple Sclerosis Chronic Progressivemedicine.diseaseImmunohistochemistryRatsBlotmedicine.anatomical_structurenervous systemBlood-Brain BarrierAstrocytescardiovascular systemInternational journal of molecular medicine
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Neurofilament is an autoantigenic determinant in myasthenia gravis

1999

Intratumorous expression of a 153-kd protein (p153), which contains an acetylcholine receptor-like epitope, is the only tumor marker described to date that significantly associates with thymoma in paraneoplastic myasthenia gravis (MG). Here, we report that p153 is identical to the midsize neurofilament, as verified by immunohistochemistry, immunofluorescence, and western blot analysis. Furthermore, the acetylcholine receptor-like epitope of the midsize neurofilament (NF-M) was identified by peptide epitope mapping. We also show, using T-cell proliferation assays, a significantly increased response of intratumorous T cells to a recombinant midsize neurofilament fragment in thymoma patients w…

Pathologymedicine.medical_specialtyThymomamusic.instrumentNeurofilamentmedicine.diagnostic_testBiologymedicine.diseaseImmunofluorescenceFollicular hyperplasiaMyasthenia gravisEpitopeNeurologyhemic and lymphatic diseasesmedicineImmunohistochemistryNeurology (clinical)musicAcetylcholine receptorAnnals of Neurology
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Computer-Assisted Classification Patterns in Autoimmune Diagnostics: The AIDA Project.

2016

International audience; Antinuclear antibodies (ANAs) are significant biomarkers in the diagnosis of autoimmune diseases in humans, done by mean of Indirect ImmunoFluorescence (IIF) method, and performed by analyzing patterns and fluorescence intensity. This paper introduces the AIDA Project (autoimmunity: diagnosis assisted by computer) developed in the framework of an Italy-Tunisia cross-border cooperation and its preliminary results. A database of interpreted IIF images is being collected through the exchange of images and double reporting and a Gold Standard database, containing around 1000 double reported images, has been settled. The Gold Standard database is used for optimization of …

Pathologymedicine.medical_specialtyTunisiaArticle SubjectAnti-nuclear antibody[SDV]Life Sciences [q-bio]lcsh:MedicineCAD02 engineering and technologyGeneral Biochemistry Genetics and Molecular Biology030218 nuclear medicine & medical imagingAutoimmune Diseases03 medical and health sciences0302 clinical medicine0202 electrical engineering electronic engineering information engineeringImage Processing Computer-AssistedMedicineHumansFluorescent Antibody Technique IndirectIndirect immunofluorescenceGeneral Immunology and Microbiologybusiness.industrylcsh:RIIfPattern recognitionGeneral MedicineGold standard (test)Computer aided detectionSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)3. Good healthFluorescence intensityItalyComputer-aided diagnosisAntibodies Antinuclear020201 artificial intelligence & image processingArtificial intelligencebusinessComputer Aided Diagnosis Immunofluorescence Pattern Classification IIF images Autoimmune diseases SVM ANN HEp-2Research ArticleBioMed research international
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A monoclonal Ro-antibody and the serum of a Ro-positive patient with subacute cutaneous lupus erythematosus (SCLE) react with basal layers of human e…

1988

Skin lesions, especially at areas exposed to sunlight, prove to be a major form of manifestation of diseases related to Ro-antibodies and neonatal-, 'ANA-negative-', and cutaneous types of lupus erythe- matosus. A monoclonal Ro-antibody established by our group reacts with a 60 kD polypeptide in extracts from human spleen, whereas in extracts from human epidermis the monoclonal Ro-antibody and a purified Ro-antibody from a monospecific serum of a patient with subacute cutaneous lupus erythematosus reacted with a 60 kD and a 48 kD protein. Performing immunofluorescence microscopy on HEp2-cells both antibodies showed a nuclear speckled staining pattern and a reaction with cytokeratin filament…

Pathologymedicine.medical_specialtymedicine.drug_classClinical BiochemistryBlotting WesternFluorescent Antibody TechniqueEnzyme-Linked Immunosorbent AssayMonoclonal antibodyImmunofluorescenceBiochemistrySubacute cutaneous lupus erythematosusmedicineLupus Erythematosus CutaneousHumansskin and connective tissue diseasesSystemic lupus erythematosusbiologyEpidermis (botany)medicine.diagnostic_testAntibodies MonoclonalGeneral Medicinemedicine.diseaseAntibodies AntinuclearMonoclonalbiology.proteinAntibodyEpidermisAnti-SSA/Ro autoantibodiesEuropean journal of clinical investigation
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Localization of antigens PwA33 and La on lampbrush chromosomes and on nucleoplasmic structures in the oocyte of the urodele Pleurodeles waltl: Light …

1994

Monoclonal antibodies A33/22 and La11G7 have been used to study the distribution of the corre-sponding antigens, PwA33 and La, on the lampbrush chromosome loops and nucleoplasmic structures of P. waltl oocytes, using immunofluorescence, confocal laser scanning microscopy and immunogold labeling. The results obtained with these antibodies have been compared with those obtained with the Sm-antigen-specific monoclonal antibody Y12. All these monoclonal antibodies (mAbs) labeled the matrices of the majority of normal loops along their whole length. Nucleoplasmic RNP granules showed a strong staining with the mAbs La11G7 and Y12 throughout their mass, but with the mAb A33/22, they showed only a …

PleurodelesTranscription Geneticmedicine.drug_classFluorescent Antibody TechniqueMonoclonal antibodyImmunofluorescenceAutoantigensChromosomeslaw.inventionPleurodeleslawGeneticsmedicineAnimalsMicroscopy ImmunoelectronGenetics (clinical)OrganellesNucleoplasmbiologymedicine.diagnostic_testAntibodies MonoclonalNuclear ProteinsImmunogold labellingbiology.organism_classificationImmunohistochemistryMolecular biologyCell biologyStainingLampbrush chromosomeRibonucleoproteinsOocytesFemaleElectron microscopeChromosoma
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Papel de la inmunofluorescencia y el diagnóstico molecular en la caracterización de la discinesia ciliar primaria

2019

Pulmonary and Respiratory MedicinePathologymedicine.medical_specialtymedicine.diagnostic_testbusiness.industrymedicineImmunofluorescencemedicine.diseasebusinessPrimary ciliary dyskinesiaArchivos de Bronconeumología
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Expression of the fibrinogen binding mannoprotein and the laminin receptor of Candida albicans in vitro and in infected tissues.

1996

We have previously reported a 37 kDa laminin-binding protein (p37) and a 58 kDa fibrinogen-binding mannoprotein (mp58) on the surface of Candida albicans. A few yeast cells expressed both functional receptors at the surface while germ tubes expressed a functional mp58 fibrinogen but not a functional p37 laminin receptor. These receptors were heterogeneously dispersed at the surface as shown by binding of rabbit antiserum to mp58 (PAb anti-mp58) and antiserum to the human high affinity laminin receptor. In this report we have used a dual fluorescence technique to determine if the two receptors colocalize, perhaps as part of a receptor complex. Fibrinogen was used as a probe for mp58 and poly…

Receptor complexBiologyImmunofluorescenceMicrobiologyReceptors LamininBacterial ProteinsLamininCandida albicansGeneticsmedicineAnimalsHumansReceptorCandida albicansFluorescent Antibody Technique IndirectMolecular BiologyAntibodies FungalAntiserumMembrane Glycoproteinsmedicine.diagnostic_testBinding proteinCandidiasisFibrinogen bindingFibrinogenbiology.organism_classificationMolecular biologyImmunohistochemistryBiochemistrybiology.proteinRabbitsCarrier ProteinsFEMS microbiology letters
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Probing human beta1- and beta2 -adrenoceptors with domain-specific fusion protein antibodies.

1997

In order to generate antibodies suitable for immunological studies on beta-adrenoceptors constitutively expressed at low levels in cells or tissues we have produced fusion proteins of the amino- and carboxy-terminus, and the second extracellular loop of the human beta 1- or beta 2-adrenoceptors with bacterial glutathione-S-transferase in E. coli. Rabbit antibodies raised against these fusion proteins strongly reacted with intact human beta 1- or beta 2-adrenoceptors in a subtype- and domain-specific manner. Antibodies directed against the second extracellular loop of the beta 1-adrenoceptor reacted stronger with non-denatured receptors and decreased the affinity of the 3H-labelled antagonis…

Recombinant Fusion ProteinsBlotting WesternEnzyme-Linked Immunosorbent AssayBiologyImmunofluorescenceProtein Structure SecondaryAntibodiesRadioligand AssayAntibody SpecificitymedicineExtracellularAnimalsHumansAvidityReceptorFluorescent Antibody Technique IndirectPharmacologymedicine.diagnostic_testMolecular biologyFusion proteinPrimary and secondary antibodiesPrecipitin TestsBlotMicroscopy FluorescenceBiochemistrybiology.proteinRabbitsReceptors Adrenergic beta-2AntibodyReceptors Adrenergic beta-1European journal of pharmacology
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Serological evidence for Borna disease virus infection in humans, wild rodents and other vertebrates in Finland

2005

Abstract Background Borna disease virus (BDV) can infect many vertebrate species, including humans. BDV infection may lead to meningoencephalomyelitis in animals. An association with human neuropsychiatric diseases has been reported, but the causal relationship between BDV and human disease remains unclear. Objectives and study design To find out whether BDV is present in Finland and to look for a potential reservoir, we examined a large panel of blood samples from different vertebrate species with immunofluorescence assay. Samples from horses, cats, dogs, sheep, cattle, large predators, grouse, wild rodents and humans were included. Most positive results were confirmed by other specific me…

Rodentvirusesanimal diseasesAntibodies ViralCat DiseasesSerologyRodent Diseases0403 veterinary scienceSeroepidemiologic StudiesDog DiseasesBorna disease virusFinland0303 health sciencesCATSmedicine.diagnostic_testvirus diseases04 agricultural and veterinary sciences3. Good healthOccupational DiseasesInfectious DiseasesViral diseaseAntibody040301 veterinary sciencesAnimals WildRodentiaBiologyImmunofluorescenceVirusCell LineVeterinariansBirds03 medical and health sciencesDogsVirologybiology.animalmedicineAnimalsHumansHorsesDisease Reservoirs030304 developmental biologySheepBird DiseasesSeroepidemiologic StudiesVirologyBorna DiseaseImmunologyCatsbiology.proteinCattleJournal of Clinical Virology
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An indirect immunofluorescent antibody technique for detection and enumeration of Vibrio vulnificus serovar E (biotype 2): delevopment and applicatio…

2000

The applications of an indirect fluorescent antibody technique (IFAT), developed to detect and enumerate the pathogenic bacterium Vibrio vulnificus serovar E from water and clinical samples, are described. This technique proved accurate for detecting V. vulnificus, even under starvation conditions and in the non-culturable state, and could differentiate this species from other bacteria which share the same habitats. The IFAT was successfully used to diagnose vibriosis from naturally- and artificially-infected eels. The overall data suggest that applying this technique properly in environmental and epidemiological/epizootiological studies could significantly increase our knowledge of this ba…

SerotypeVibrio vulnificusImmunofluorescenceSensitivity and SpecificityApplied Microbiology and BiotechnologyMicrobiologyFish DiseasesVibrionaceaeVibrio InfectionsEnumerationmedicineAnimalsSeawaterFluorescent Antibody Technique IndirectVibrioEelsbiologymedicine.diagnostic_testfungiGeneral Medicinebacterial infections and mycosesbiology.organism_classificationAntibodies BacterialVibrioVibrio InfectionsWater MicrobiologyBacteriaBiotechnologyJournal of Applied Microbiology
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