Improved Live Attenuated Brucella Vaccines to Reduce Human Diseases
Improved Live Attenuated Brucella Vaccines to Reduce Human Diseases
批准号:
8933356
负责人:
THOMAS A FICHT
金额:
$58.55万
依托单位国家:
美国
项目类别:
财政年份:
2015
资助国家:
美国
项目状态:
已结题
起止时间:
2015-08-20 至 2018-06-30
关键词:
AddressAdverse effectsAgricultureAnimal DiseasesAnimalsAntigensAnusAreaAttenuatedAttenuated Live Virus VaccineBrucellaBrucella VaccineBrucellosisCombined VaccinesConsumptionCountryCrude ExtractsDataDeveloping CountriesDevelopmentDiagnosticDiagnostic testsEconomicsEducationEnvironmental PollutionEvaluationExcisionFailureFamilyFamily suidaeGenesGoalsGoatHeatingHumanImmuneImmune systemIn VitroInfectionInjectableKnowledgeLaboratoriesLifeLivestockMethodsMicroencapsulationsModelingMusMutationNutritional RequirementsOralOrganismOutcomeOutcome StudyPopulationPregnancyPreparationProductivityPublic HealthRecombinantsRelative (related person)ResearchResearch InfrastructureResearch PersonnelResidual stateRiskRuminantsSafetySocioeconomic StatusSourceStagingSystemTestingTimeLineTranslatingVaccinatedVaccinationVaccine DesignVaccinesViralVirulenceWorkZoonosesabortionbasecontrolled releasedisorder controlexpectationhuman diseaseimprovedin vivo Modelinnovationkillingsmouse modelmutantnonhuman primatenutritionpregnantpreventprogramspublic health relevanceresearch studysocioeconomicssuccesstransmission processvaccine candidatevaccine developmentvaccine safety
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The goal of the proposed research is the development of vaccines against Brucella infection that are safe and efficacious. Our general approach is focused on the use of live attenuated vaccines, LAVs. While vaccines developed from heat-killed organisms, crude extracts or recombinant subunits have demonstrated little efficacy, Brucella LAVs have proven highly effective when used in conjunction with test and slaughter. However, when applied to under-developed countries such programs can result in significant losses in animal productivity and family livelihood and as such enforcement is lax. Currently available Brucella vaccines are unsafe for use either directly in gestating animals or humans. Furthermore, their use in animals poses a secondary risk to public health especially in underdeveloped countries where livestock are a primary source of nourishment. For these reasons, we have sought to identify improved LAVs that are safe for use in animals at all stages of gestation, and, therefore, pose a reduced risk to humans. Ongoing experiments in nonhuman primates have confirmed a level of safety that provides continued support for a parallel goal of developing a Brucella vaccine that is safe for human use. Successful demonstration of safety in goats is also expected to provide support for reduced biocontainment level allowing examination of efficacy in goats. The overall design of the vaccine combines the optimal features of a LAV that is safe, free of side effects in animals and efficacious with a delivery system that provides enhanced immune stimulation through microencapsulation. The successful outcome of these studies will be used to produce a vaccine that provides significant protection against abortion and to enhance animal productivity while also restricting human infection including environmental contamination. However, drawbacks of live attenuated vaccines include the concern of reversion to virulence. For this reason, we have proposed an evaluation of secondary mutations that may be expected to effectively "lock" the organism into an attenuated state while providing a diagnostic test capable of distinguishing vaccines from infected animals. The need for improved Brucella vaccines is highly warranted due to continue human infection worldwide (500,000 new cases annually) resulting from close association with or consumption of agricultural animal products. Recent dramatic increases worldwide in wild and feral swine populations also act as reservoirs of human infection, as well as agricultural species. This concern is exacerbated by a lack of knowledge concerning mechanisms of immune protection and the potential use of Brucella spp. as bioweapons.
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会议论文
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财政年份:2009
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财政年份:2008
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财政年份:2001
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依托单位:
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批准号:6532844
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项目类别:
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资助金额:$27.65万
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财政年份:2001
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依托单位:
Improved Brucella Vaccine Strains
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批准号:7540374
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项目类别:
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资助金额:$34.65万
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依托单位:
Improved Brucella Vaccine Strains
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批准号:6605772
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项目类别:
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资助金额:$29.1万
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财政年份:2001
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依托单位:
Improved Brucella Vaccine Strains
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批准号:7324823
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项目类别:
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资助金额:$34.65万
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财政年份:2001
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依托单位:
Improved Brucella Vaccine Strains
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财政年份:2000
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依托单位:
Improved Brucella Vaccine Strains
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财政年份:2000
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依托单位:
Improved Brucella Vaccine Strains
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批准号:6998471
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项目类别:
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资助金额:$35.52万
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财政年份:2000
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负责人:THOMAS A FICHT
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依托单位:
Evaluation fo Live Attenuated B. Melitensis Vaccines in Nonhuman Primates
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项目类别:
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资助金额:$92.96万
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财政年份:--
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负责人:THOMAS A FICHT
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依托单位:
Evaluation fo Live Attenuated B. Melitensis Vaccines in Nonhuman Primates
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批准号:8042581
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项目类别:
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资助金额:$51.51万
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财政年份:--
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负责人:THOMAS A FICHT
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依托单位:
海外基金