Mechanism of alphavirus packaging: designing of pseudoinfectious viruses
Mechanism of alphavirus packaging: designing of pseudoinfectious viruses
批准号:
8415830
负责人:
ILYA V. FROLOV
金额:
$34.43万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-02-01 至 2017-01-31
关键词:
AdjuvantAdverse reactionsAlphavirusAlphavirus InfectionsAnimal ModelAnimalsAntigensAntiviral AgentsAntiviral ResponseAttenuatedAttenuated Live Virus VaccineAttenuated VaccinesCapsidCapsid ProteinsCellsCellular ImmunityCharacteristicsChickensCodon NucleotidesDNA-Directed RNA PolymeraseDataDefective VirusesDevelopmentDiseaseDoseEmbryoEncephalitis VirusesEncephalomyocarditis virusEquilibriumEquine EncephalomyelitisFamilyGenesGenomeGenomicsHealthHomologous ProteinHumanHuman poliovirusImmune responseImmunityImmunocompromised HostIn VitroInactivated VaccinesInfectionInflammatory ResponseInsectaInternal Ribosome Entry SiteKnowledgeLifeMeasuresMicroRNAsMolecularMutateMutationNuclearPathogenesisPathogenicityPhenotypePoint MutationPoliovirusesProcessProductionPublic HealthRNARNA replicationResearchResearch ProposalsResidual stateSafetySanitationSerial PassageSignal TransductionStructural ProteinStructureSystemTestingTissuesTogaviridaeVaccinationVaccinesVariantVero CellsViralViral ProteinsViral VaccinesViremiaVirionVirusVirus ReplicationVirus-like particleWaterattenuationbasebiodefensedesignin vivomutantneutralizing antibodynovel strategiesparticlepathogenplasmid DNApreventprogramsrecombinant virusstructural viral genestissue culturetransmission processvaccine candidatevaccine developmentviral RNA
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The Alphavirus genus in the Togaviridae family contains a variety of widely distributed important human and animal pathogens. Venezuelan (VEEV), eastern (EEEV) and western (WEEV) equine encephalitis viruses represent a serious public health threat in the US and can be applied by bioterrorists. However, to date, neither effective antiviral nor safe and efficient vaccines have been developed for preventing any of these infections. The existing experimental vaccines are either of poor efficacies or demonstrate very strong adverse reactions in humans. Our recent studies of the molecular mechanism of alphavirus RNA packaging led to understanding of structure and function of the alphavirus RNA-specific packaging signal, which is present in the genomes of other encephalitogenic alphaviruses and recognized by both homologous and capsid proteins. These data will be applied in the proposed research to develop fundamentally new strategies of designing live alphavirus variants possessing irreversible, highly attenuated phenotypes, but producing virus-specific antigens, required for induction of sterilizing immunity as efficiently as a wt virus. By introducing multiple, rationally designed mutations into capsid protein or newly identified universal RNA packaging signal, we will develop alphaviruses that retain high levels of RNA replication, and production of structural proteins which are released either mostly (strategy 1) or
exclusively (strategy 2) in the form of non-infectious, genome-free virus-like particles and, thus,
develop no viremia in vivo. These viruses will be capable of inducing a balanced combination of cellular immune response and high levels of neutralizing antibodies.
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会议论文
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