Transmission-blocking live vaccine for Chagas disease
Transmission-blocking live vaccine for Chagas disease
批准号:
8390470
负责人:
Rick L Tarleton
金额:
$34.9万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-12-01 至 2016-11-30
关键词:
AnimalsAntibody FormationAntigensAttenuatedAttenuated Live Virus VaccineAttenuated VaccinesB-LymphocytesBacteriaBiological AssayBloodCD8B1 geneCanis familiarisCell LineChagas DiseaseCharacteristicsCommunicable DiseasesCompanionsDevelopmentEquilibriumEvaluationExposure toFamilyFelis catusFlagellinFutureGenesGeneticGenetic RecombinationGoalsHome environmentHumanImmuneImmune responseImmunityIn VitroIndividualInfectionInfection ControlInfection preventionInsectaKnock-outLaboratoriesLatin AmericaLengthLifeLigandsLinkLivestockMetricModificationMonitorMusNeisseria meningitidisOralOrganismParasitemiaParasitesParasitic DiseasesPreventionProtein SecretionProteinsRelative (related person)RouteSafetySalmonellaSiteSourceSubunit VaccinesSystemT cell responseT-LymphocyteTLR5 geneTestingTimeToll-like receptorsTriatomaTrypanosoma cruziUnited StatesVaccinatedVaccinationVaccinesVariantVirulenceVirulentWorkcompanion animalfield studyflexibilityin vivoknockout genemouse modeloverexpressionpathogenpreventprophylacticresearch studyresponsesuccesstooltransmission processvaccine developmentvaccine safetyvaccine-induced immunityvector
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Vaccine development for human parasitic diseases has not been a fruitful endeavor to date, in part due to the genetic complexity of these eukaryotic pathogens and the relative lack of understanding of effective host immune responses to, and immune evasion mechanisms used by them. In many sites, the transmission of Trypanosoma cruzi to insects - and subsequently to the people - is nearly totally determined by the presence or absence of T. cruzi infected dogs or cats in the home. Logistically what this means is that vaccination of dogs and cats so that they are not infectious to bugs could be a highly effective tool for the prevention human infections. We propose the development of avirulent lines of T. cruzi and their evaluation as vaccines to prevent the transmission of T. cruzi from companion or livestock animals to insects. Using the specific deletion of T. cruzi genes we will develop avirulent lines, selecting for their ability to grow well as epimastigotes and to convert to infective metacyclic trypomastigotes, to infect cells lines in vitro, to induce strong T cell and antibody responses in vivo in mice and ultimately, to prevent the development of detectable parasitemia in mice and dogs following challenge with virulent parasite lines. We will optimize the gene knockout (KO) avirulent lines to enhance their potency and safety by overexpression of low copy genes encoding non-variant T. cruzi proteins as well as by the expression and secretion of the heterologous protein TLR ligands from bacteria. These modifications are expected to accelerate and potentiate the immune response to T. cruzi. Among the enticing aspects of this approach is that a vaccine for companion animals would not have to absolutely prevent infection - just keep parasite levels in the blood of these animals below the level of transmissibility to insects. Additionally, such a vaccine could be delivered in an oral form - making widespread vaccination of animals quite easy.
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