课题基金 / 基金详情

Vaccine Development for Burkholderia amllei and B. pseudomallei

Vaccine Development for Burkholderia amllei and B. pseudomallei
鼻疽伯克霍尔德杆菌和类鼻疽伯克霍尔德杆菌的疫苗开发
批准号:
7676555
负责人:
Don MARK ESTES
金额:
$45.17万
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:
2009-04-15 至 2014-02-28
关键词:
Acute DiseaseAdjuvantAerosolsAnimal Disease ModelsAnimalsAntibioticsAntibody FormationAntigensAttenuated VaccinesBacteriaBiologicalBiological MarkersBiological WarfareBurkholderiaBurkholderia InfectionsBurkholderia malleiBurkholderia pseudomalleiCarrier ProteinsCategoriesCellsCharacteristicsChemicalsChildCodeConjugate VaccinesContainmentControlled StudyCouplingData SetDevelopmentDiseaseDisease modelDolphinsDoseDrug FormulationsElderlyEnvironmentEvaluationFlagellaFlagellinGenerationsGeneticGenomeGlandersGlycoconjugatesGoalsGram-Negative BacteriaHaemophilus influenzaeHost resistanceHumanImmuneImmune SeraImmune responseImmunityImmunocompromised HostImmunoglobulin MIndividualInfectionLaboratory miceLicensingLicensureLinkLipopolysaccharidesMacacaMalleusMediatingMedicalMelioidosisMethodsModelingMusNeisseria meningitidisNon obeseO AntigensOrganismPan GenusPharmaceutical PreparationsPolysaccharidesPopulationPregnant WomenProcessProductionProteinsPublishingRecombinant ProteinsRecombinantsReportingResourcesRouteSafetySalmonella typhiSevere Combined ImmunodeficiencyStreptococcus pneumoniaeStudy SectionSubunit VaccinesSurfaceSystemT-LymphocyteTechnologyTexasUnited States Food and Drug AdministrationUniversitiesVaccinesVirulence FactorsWhole Cell VaccineWorkaustinbasebiodefensecandidate selectioncapsulecell killingcell mediated immune responsecombatcomparative efficacycostdiabeticdiabetic ratgenome sequencinggenome-widehumanized SCID mouseimmunogenicimmunogenicitykillingsmicroorganismnamed groupnonhuman primatepathogenprophylacticresponsesafety studyvaccine candidatevaccine deliveryvaccine developmentweapons

项目摘要

项目成果

Don MARK ESTES的其他基金

相似基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
This proposal is directed towards the development of vaccines for the category B agents Burkholderia pseudomallei and Burkholderia mallei. There is an urgent and acknowledged need to develop better Drophylactic countermeasures through the use of vaccines and immune stimulants for both melioidosis and glanders. We believe it is appropriate to consider these pathogens in parallel in this project because they are closely related at a genetic level, and there is a possibility that common approaches to these diseases can be identified. The aims of this project are to: (1) Identify optimal delivery systems and protein carriers. (2) Develop optimized protein-polysaccharide conjugation methods. (3) Compare efficacy of homologous versus heterologous protein-polysaccharide conjugates. (4) Identify biomarkers and mechanisms of vaccine-mediated protection in acute disease models, including the laboratory mouse, the humanized SCID mouse, and nonhuman primate models. Our principal aim is to devise a non-living vaccine which is able to protect against both 6. pseudomallei and 8. mallei infection. This is an important consideration for eventual licensure and use with potential applications for special populations such as young children, the elderly, pregnant women and immunocompromised subjects. Ultimately, the studies outlined in this proposal will establish a data set to begin the process of a successful submission of an investigative new drug (IND) application to the Food and Drug Administration.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Vaccine Development for Burkholderia amllei and B. pseudomallei
Non-invasive Optical Imaging of Select Agent Bacteria in Non-human Primates
Non-invasive Optical Imaging of Select Agent Bacteria in Non-human Primates
Discovery of subunit vaccine candidates against glanders
海外基金