Developing an in vitro system for HCV propagation
Developing an in vitro system for HCV propagation
批准号:
7924252
负责人:
Ratna B. Ray
金额:
$3.31万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-22 至 2010-08-31
关键词:
AddressAntibodiesAntiviral AgentsApplications GrantsAreaBiological AssayCD81 geneCell Culture SystemCell Culture TechniquesCellsComputer Systems DevelopmentDetectionDevelopmentExhibitsFutureGenomeGenotypeGeographic LocationsGoalsGrowthHepatitis CHepatitis C virusHepatocyteHumanImmunofluorescence ImmunologicImmunohistochemistryIn VitroInfectionInfectious hepatitidesInterferon-alphaMolecular CloningMutationPan GenusPharmaceutical PreparationsProductionRNARNA replicationRenilla LuciferasesReporterReporter GenesReportingResearch PersonnelResistanceScreening procedureSerial PassageSerumSystemTherapeuticTitrationsTransfectionVaccinesVariantVirionVirusVirus DiseasesWorkbaseeffective therapyhigh throughput screeningimprovedinhibitor/antagonistnovelparticleprogramspublic health relevancerecombinant virustherapeutic vaccinetoolvaccine evaluationviral RNA
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Hepatitis C virus (HCV) often causes a prolonged and persistent infection in humans, and there is an urgent need for the development of a highly effective therapy and vaccine. Distinct genotypes and subtypes of HCV exist in different geographic locations. Infection with HCV genotype 1 (subtypes a and b) is prevalent in the USA, and is relatively resistant to available therapies. Recently, HCV growth in cell culture has been reported by us and other investigators. Majority of the work was done with HCV genotype 2a (JFH1 strain) in Huh7 cells or its derivatives. We have developed growth of HCV genotype 1a (H77 strain) in immortalized human hepatocytes (IHH). However, wild type HCV 1a yield is low and a significant sequence variation exists between HCV H77 and JFH1 strains. Although, HCV 1a particles are generated, virus growth from serial passages in hepatocytes has not been established. Therefore, it is extremely important to have a robust cell culture system for HCV 1a growth. Furthermore, titration of infectious virus particles is restricted with immunofluorescence or immunohistochemistry based assay. In this Developmental R21 grant application, we plan to generate a high titer HCV 1a by characterizing virus growth in IHH following different approaches, and develop a convenient readout for virus infection using a reporter assay. The results from the proposed work will help in further developing novel areas, including high throughput assay for antiviral screening with tremendous impact for drug and vaccine discovery programs. PUBLIC HEALTH RELEVANCE: Hepatitis C virus (HCV) often causes a prolonged and persistent infection in humans, and there is an urgent need for the development of highly effective therapy and vaccine. We have recently generated HCV in cell culture. We will study to improve the in vitro growth of this virus and develop a sensitive readout for future use in high throughput antiviral screening and vaccine discovery programs.
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会议论文
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批准号:7895338
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依托单位:
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批准号:8101849
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资助金额:$31.44万
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批准号:7741066
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依托单位:
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资助金额:$34.09万
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依托单位:
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资助金额:$18.31万
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依托单位:
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依托单位:
海外基金