Search results for "HEPATITIS C VIRUS"

showing 10 items of 403 documents

Epidemiology of hepatitic C infection in hemodialysis patients of Sicily

2008

Hepatitis C virus hemodialysis patients epidemiology
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Quantitation of HCV-replication using one-step competitive reverse transcription-polymerase chain reaction and a solid phase, colorimetric detection …

1994

A solid phase assay for the colorimetric detection of competitively amplified HCV-cDNA has been established and used to investigate clinical samples from patients with chronic hepatitis. The assay is based on the reduction in the amplification of an hepatitis C virus-related competitor molecule by wild-type hepatitis C virus during polymerase chain reaction. The internal standard contains a lac operator sequence, allowing the amount of amplified competitor to be determined using a lac I-repressor/beta-galactosidase fusion protein. The reduction in the amplification of competitor is dependent upon the concentration of HCV-RNA in the original sample. External hepatitis C virus wild-type stand…

Hepatitis C virusHepacivirusBiologymedicine.disease_causeVirus ReplicationPolymerase Chain ReactionSensitivity and SpecificityViruslaw.inventionFlaviviridaelawmedicineHumansPolymerase chain reactionHepatologyGene AmplificationHepatitis CAmpliconmedicine.diseasebiology.organism_classificationVirologyMolecular biologyHepatitis CReverse transcription polymerase chain reactionTiterRNA ViralColorimetryJournal of hepatology
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Characterization of cell lines carrying self-replicating hepatitis C virus RNAs.

2001

ABSTRACT Subgenomic selectable RNAs of the hepatitis C virus (HCV) have recently been shown to self-replicate to high levels in the human hepatoma cell line Huh-7 (V. Lohmann, F. Körner, J. O. Koch, U. Herian, L. Theilmann, and R. Bartenschlager, Science 285:110–113, 1999). Taking advantage of this cell culture system that allows analyses of the interplay between HCV replication and the host cell, in this study we characterized two replicon-harboring cell lines that have been cultivated for more than 1 year. During this time, we observed no signs of cytopathogenicity such as reduction of growth rates or ultrastructural changes. High levels of HCV RNAs were preserved in cells passaged under…

Hepatitis C virusImmunoelectron microscopyImmunologyHepacivirusBiologyViral Nonstructural Proteinsmedicine.disease_causeVirus ReplicationMicrobiologyViral ProteinsVirologymedicineTumor Cells CulturedHumansRepliconPhosphorylationNS5ARNAVirologyMolecular biologyVirus-Cell InteractionsNS2-3 proteaseViral replicationCell cultureInsect ScienceRNA ViralRepliconJournal of virology
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Anti-rat liver microsomal and cytosolic antibodies in hepatitis C virus infection.

1994

In order to assess the frequency of autoimmunity markers in hepatitis C virus infection, 229 RIBA 2 HCV positive individuals were tested by ELISA and Immunoblot assay using as antigen rat liver microsomal and cytosolic proteins. Twenty-one out of 229 individuals (9%) showed anti-rat liver microsome antibodies by ELISA, but the titre was low (1:100 to 1:1,600). In Immunoblot, only 5 of these 21 ELISA positive sera recognized also rat liver microsomal proteins (MW between 30 to 64 kDa). Antibodies against rat liver cytosolic proteins were found by ELISA in 14 out of 229 individuals (6%). Three of them showed a reactivity in Immunoblot to 42 kDa or 55 kDA proteins. In conclusion, HCV infection…

Hepatitis C virusImmunologyImmunoblottingEnzyme-Linked Immunosorbent AssayAutoimmune hepatitismedicine.disease_causeVirusAutoimmunityCytosolAntigenmedicineImmunology and AllergyAnimalsHumansRats WistarAutoantibodiesAutoimmune diseasebiologyAutoantibodymedicine.diseaseVirologyHepatitis CRatsLiverbiology.proteinMicrosomes LiverFemaleAntibodyAutoimmunity
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Sequences in the 5′ Nontranslated Region of Hepatitis C Virus Required for RNA Replication

2001

ABSTRACT Sequences in the 5′ and 3′ termini of plus-strand RNA viruses harbor cis -acting elements important for efficient translation and replication. In case of the hepatitis C virus (HCV), a plus-strand RNA virus of the family Flaviviridae , a 341-nucleotide-long nontranslated region (NTR) is located at the 5′ end of the genome. This sequence contains an internal ribosome entry site (IRES) that is located downstream of an about 40-nucleotide-long sequence of unknown function. By using our recently developed HCV replicon system, we mapped and characterized the sequences in the 5′ NTR required for RNA replication. We show that deletions introduced into the 5′ terminal 40 nucleotides abolis…

Hepatitis C virusImmunologyRNA-dependent RNA polymeraseReplicationHepacivirusmedicine.disease_causeOrigin of replicationMicrobiologyVirologymedicineTumor Cells CulturedHumansRepliconGeneticsbiologyRNARNA virusbiology.organism_classificationVirologyNS2-3 proteaseInternal ribosome entry siteInsect ScienceProtein BiosynthesisRNA ViralReplicon5' Untranslated Regions
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Mutations in hepatitis C virus RNAs conferring cell culture adaptation.

2001

ABSTRACT As an initial approach to studying the molecular replication mechanisms of hepatitis C virus (HCV), a major causative agent of acute and chronic liver disease, we have recently developed selectable self-replicating RNAs. These replicons lacked the region encoding the structural proteins and instead carried the gene encoding the neomycin phosphotransferase. Although the replication levels of these RNAs within selected cells were high, the number of G418-resistant colonies was reproducibly low. In a search for the reason, we performed a detailed analysis of replicating HCV RNAs and identified several adaptive mutations enhancing the efficiency of colony formation by several orders of…

Hepatitis C virusImmunologyReplicationHepacivirusBiologyViral Nonstructural Proteinsmedicine.disease_causeMicrobiologychemistry.chemical_compoundVirologymedicineTumor Cells CulturedHumansRepliconAmino AcidsNS5BGene3' Untranslated RegionsGeneticsMutationThree prime untranslated regionRNAVirologyAdaptation PhysiologicalchemistryCell cultureInsect ScienceMutationRNA ViralRepliconJournal of virology
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Refined analysis of genetic variability parameters in hepatitis C virus and the ability to predict antiviral treatment response.

2008

Summary.  Hepatitis C virus (HCV) infects approximately 3% of the world population. The chronicity of hepatitis C seems to depend on the level of genetic variability. We have recently (Torres-Puente et al., J Viral Hepat, 2008; 15: 188) reported genetic variability estimates from a large-scale sequence analysis of 67 patients infected with HCV subtypes 1a (23 patients) and 1b (44 patients) and related them to response, or lack of, to alpha-interferon plus ribavirin treatment.. Two HCV genome regions were analysed in samples prior to antiviral therapy, one compressing the three hypervariable regions of the E2 glycoprotein and another one including the interferon sensitive determining region …

Hepatitis C virusMutation MissenseAlpha interferonHepacivirusBiologyViral Nonstructural Proteinsmedicine.disease_causeAntiviral AgentsNucleotide diversityViral Envelope ProteinsVirologyDrug Resistance ViralRibavirinmedicineHumansGenetic variabilityNS5AGeneticsHepatologyHaplotypeGenetic VariationHepatitis CHepatitis C Chronicmedicine.diseaseVirologyHypervariable regionInfectious DiseasesTreatment OutcomeHaplotypesInterferonsJournal of viral hepatitis
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Hepatitis C virus antibody secretion in vitro by peripheral blood lymphocytes.

1992

A recombinant polypeptide corresponding to a virus-specific cDNA clone (c100-3) serves as the antigen for a hepatitis C virus (HCV) antibody assay. Previous investigations have shown an 80% prevalence of HCV antibodies in sera of patients suffering from post-transfusional chronic hepatitis non-A, non-B, but positive results were also obtained for 30 to 70% of sera from patients with chronic hepatitis B or autoimmune hepatitis. In this study we show that HCV antibodies are secreted by peripheral blood lymphocytes (PBL) in vitro. PBL from 12/35 patients with chronic non-A, non-B hepatitis and 1/6 patients with chronic active hepatitis B spontaneously secreted HCV antibodies in cell culture su…

Hepatitis C virusT-LymphocytesEnzyme-Linked Immunosorbent AssayAutoimmune hepatitisHepacivirusBiologymedicine.disease_causeLymphocyte ActivationVirusAntigenmedicineHumansHepatitis AntibodiesLymphocytesHepatitisB-LymphocytesHepatologyvirus diseasesT-Lymphocytes Helper-Inducermedicine.diseaseVirologydigestive system diseasesPolyclonal antibodiesHumoral immunityImmunologybiology.proteinAntibodyJournal of hepatology
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ELITA consensus statements on the use of DAAs in liver transplant candidates and recipients

2017

International audience; The advent of safe and highly effective direct-acting antiviral agents (DAAs) has had huge implications for the hepatitis C virus (HCV) transplant field, and changed our management of both patients on the waiting list and those with HCV graft re-infection after liver transplantation (LT). When treating HCV infection before LT, HCV re-infection of the graft can be prevented in nearly all patients. In addition, some candidates show a remarkable clinical improvement and may be delisted. Alternatively, HCV infection can be treated post-LT either soon after the transplant, taking advantage of the removal of the infected native liver, or at the time of disease recurrence, …

Hepatitis C chronicDrugmedicine.medical_specialtyConsensusAntiviral agentmedicine.medical_treatmentHepatitis C virusmedia_common.quotation_subjectWaiting listDiseaseGuidelineLiver transplantationGuidelinesmedicine.disease_cause03 medical and health sciences0302 clinical medicineMED/12 - GASTROENTEROLOGIAMedicineHumansDrug InteractionsIntensive care medicinemedia_commonLiver transplant candidateLiver transplantationHepatologybusiness.industryWaiting listsLiver failure[SDV.MHEP.HEG]Life Sciences [q-bio]/Human health and pathology/Hépatology and GastroenterologyRecurrent hepatitis CDirect Antiviral AgentHepatitis C3. Good healthSurgerychronicAntiviral agentsWaiting list030220 oncology & carcinogenesisInterferon030211 gastroenterology & hepatologyLiver transplant recipientInterferonsbusinessComplication
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Novel artemisinin derivatives with potential usefulness against liver/colon cancer and viral hepatitis.

2013

Antitumor and antiviral properties of the antimalaria drug artemisinin from Artemisia annua have been reported. Novel artemisinin derivatives (AD1-AD8) have been synthesized and evaluated using in vitro models of liver/colon cancer and viral hepatitis B and C. Cell viability assays after treating human cell lines from hepatoblastoma (HepG2), hepatocarcinoma (SK-HEP-1), and colon adenocarcinoma (LS174T) with AD1-AD8 for a short (6h) and long (72h) period revealed that AD5 combined low acute toxicity together with high antiproliferative effect (IC50=1-5μM). Since iron-mediated activation of peroxide bond is involved in artemisinin antimalarial activity, the effect of iron(II)-glycine sulfate …

Hepatitis Viral HumanCell SurvivalvirusesHepatitis C virusClinical BiochemistryArtemisia annuaPharmaceutical SciencePharmacologymedicine.disease_causeVirus ReplicationBiochemistrychemistry.chemical_compoundCell Line TumorDrug DiscoverymedicineAnimalsHumansArtemisininMolecular BiologyCell ProliferationHepatitis B virusHepatitisbiologyMolecular StructureChemistryOrganic ChemistryLiver Neoplasmsbiology.organism_classificationmedicine.diseaseVirologyArtemisininsColonic NeoplasmsMolecular MedicineLiver cancerViral hepatitisHeminmedicine.drugBioorganicmedicinal chemistry
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