A novel vaccine against vaginal Chlamydia trachomatis
A novel vaccine against vaginal Chlamydia trachomatis
批准号:
8310567
负责人:
DEBORAH Anne DEAN
金额:
$30.0万
依托单位:
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:
2012-06-05 至 2014-05-31
关键词:
Antibody FormationAntigen-Presenting CellsAntigensBase SequenceCatechinCellsChimera organismChlamydia trachomatisClinical TrialsCommon iliac lymph nodeDataDevelopmentDoseDrug FormulationsEctopic PregnancyEpithelial CellsFlavonoidsHIVHIV-1HomingHumanImmuneImmune responseImmunityImmunizationIndividualInfectionInfertilityLaboratoriesLeadLifeLymphocyte antigenMeasuresMediatingMedicalMembraneMethodsModelingMorbidity - disease rateMucous MembraneMusMustardOilsPelvic Inflammatory DiseasePhasePopulationPositioning AttributePreparationPublishingRegimenResearchRiskRouteSafetySamplingScheduleSeedsSequence HomologySerumSexually Transmitted DiseasesSmall Business Technology Transfer ResearchSpleenSystemTestingVaccinatedVaccinationVaccine DesignVaccinesVaginaVitamin AVitamin Ebasechronic pelvic paincostcytokinedesigngranzyme Bhigh riskimmunogenicityimprovedmeetingsnovelnovel vaccinespreventprotective efficacyresponsesuccesstransmission processvaccine candidatevaginal transmission
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Preventing Chlamydia trachomatis (Ct) infections represent a critical unmet medical need. Development of an effective vaccine would not only reduce the morbidity associated with these infections, including pelvic inflammatory disease (PID), infertility, chronic pelvic pain and ectopic pregnancy, but could also reduce collateral riss including HIV transmission. Despite decades of efforts, no vaccine is currently available. The ability to generate a useful vaccine has been limited by 1) the lack of an effective method to deliver antigens that will elicit protective humeral and cell-mediated responses, and 2) the identification of specific antigenic sequences that would protect individuals from the Ct strains that cause sexually transmitted diseases (STD). The proprietary nutritive immune-enhancing delivery system (NIDS) developed by EpitoGenesis, Inc. and the broad-based sequence assessment performed by the Dean lab, in addition to the exciting preliminary data on an Ct and HIV-1 vaccine constructs, provide a unique opportunity to finally obtain an efficacious vaccine that can protect against vaginal transmission of Ct through the use of the novel antigenic constructs formulated with the novel, safe and effective NIDS for mucosal and systemic vaccinations. Furthermore, combinations of mucosal and systemic vaccination routes, lack of sequence homology to human antigens, and promising preliminary results from both EpitoGenesis and the Dean lab warrant a novel vaccine design and vaccination approach that hold promise of success.
PUBLIC HEALTH RELEVANCE: The proprietary, Chlamydia trachomatis (Ct) antigenic constructs developed by Dr. Deborah Dean, and the nutritive immune-enhancing delivery system (NIDS) developed by EpitoGenesis, provide a unique opportunity to develop an efficacious vaccine that can protect against vaginal transmission of Ct.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
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海外基金