Yellow Fever, rDNA (EP+IL-12) and rAd35 as Vectors for AIDS Vaccine Development
Yellow Fever, rDNA (EP+IL-12) and rAd35 as Vectors for AIDS Vaccine Development
批准号:
8688135
负责人:
David I Watkins
金额:
$194.7万
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:
2012-07-01 至 2017-06-30
关键词:
AIDS vaccine developmentAcuteAddressAdenovirusesAnimalsAreaAttenuatedChronic PhaseClinical TrialsControl AnimalCytomegalovirusDataDoseElectroporationFigs - dietaryGaggingGenesGenomeHIVHIV vaccineHumanImmune responseImmunityImmunizationIntentionInterleukin-12MacacaMacaca mulattaMethodsMuscleNIH Program AnnouncementsOpen Reading FramesOutcomePhasePlasmidsProteinsProteomeRNARecombinant DNARecombinant Interleukin-12RecombinantsRegimenResearchRoleSIVSeriesSerotypingT cell responseTestingTissuesVaccinatedVaccinationVaccine DesignVaccinesViralViral Load resultViremiaVirusVirus ReplicationWorkYellow FeverYellow Fever Vaccinedesignimprovedlymph nodesnonhuman primatenovel vaccinesplasmid DNApreventpublic health relevancerectalresearch studyvaccine developmentvector
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): We plan to explore whether the highly successful attenuated yellow fever (YF-17D) vaccine, rDNA delivered by electroporation along with IL-12 and rAd35 can be used as vectors to express SIV proteins in a prime/boost regimen for vaccination against the AIDS virus. In a highly integrated series of experiments, we will first define the best viral targets for a vaccine. We will then bring the results together in a final efficacy experiment to test the vectors that, if successful, could prevent suffering by millions of
people worldwide. Our application seeks to address four of the ten research areas outlined in the HIVRAD program announcement. Our project has the potential to impact HIV vaccine development on two fronts. First, we will define the targets of a successful vaccine in a challenge experiment. This will allow us to design a vaccine encoding the critical targets of a successful immune response. Second, we will develop three entirely novel vaccine vectors. If we are successful in this endeavor, our results will have a profound effect on HIV vaccine design.
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会议论文
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DEVELOPMENT OF IMMUNE MONITORING REAGENTS AND MHC TYPING TECHNOLOGIES
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依托单位:
A NOVEL, LOGICAL APPROACH TO HIV VACCINE DEVELOPMENT
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IMMUNOGENICITY AND PROTECTION OF LIVE ATTENUATED SIV239 DELTA NEF IN RHESUS
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依托单位:
MINIGENE VACCINATION WITH EARLY PRESENTED VIRAL PROTEINSAIDS RELATED RESEARCH
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SIV-specific Mamu-E-restricted CD8+ T cells
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CRYPTIC ORFS AS A VACCINE FOR HIV
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依托单位:
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依托单位:
MHC TYPING OF MACAQUES USED IN AIDS RESEARCH
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MHC-BOUND, SIV-DERIVED, CTL AND HTL EPITOPES
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依托单位:
海外基金