Rational design and targeted selection of DNA-scaffolded nicotine vaccines
Rational design and targeted selection of DNA-scaffolded nicotine vaccines
批准号:
8531045
负责人:
YUNG CHANG
金额:
$110.69万
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-04-15 至 2016-02-29
关键词:
AdjuvantAdverse effectsAnimalsAntibodiesAntibody FormationAntigensB-LymphocytesBehaviorBehavior assessmentBenchmarkingBioinformaticsBiologicalBiological AssayBrainCD4 Positive T LymphocytesCarbohydratesComplexDNADNA MaintenanceDNA StructureDataDependenceDevelopmentDiseaseDrug KineticsEpitopesEvaluationFundingGenerationsGrantImmuneImmunityImmunizationImmunoglobulin-Secreting CellsImmunologistImmunologyIn VitroIndividualInfectious AgentInterdisciplinary StudyInvestigational DrugsLeadLegal patentLengthLettersLigandsLinkLipidsMemory B-LymphocyteMinnesotaModelingModificationNanostructuresNational Institute of Drug AbuseNatureNicotineNicotine DependenceOligonucleotidesPeptidesPharmacologyPhasePositioning AttributeProceduresProductionProtocols documentationRattusReactionSafetyScientistSelf AdministrationSeriesServicesStagingStructural ChemistryStructureSynthetic VaccinesT-Cell ActivationTLR7 geneTestingToxic effectTumor AntigensVaccinesbasebehavioral pharmacologycigarette smokingdensitydesigndesign and constructiondrug developmentdrug of abuseefficacy evaluationefficacy testingimmunogenicimmunogenicityin vivointerestmortalitynanonew technologynovelprogramspublic health relevanceresponsescaffoldsmoking cessationvaccine candidatevaccine developmentvaccine efficacy
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Cigarette smoking causes various types of diseases with a high mobility and mortality. Yet, it is very difficult to quit smoking, largely due to nicotne dependence. Although nicotine vaccines have emerged as a possible strategy to reduce nicotine addiction the efficacy of existing nicotine vaccines has been disappointing, possibly attributed to their insufficient induction of nicotine-specific immunity. In this application, we propose to develop a new technology to rationally design and construct nicotine vaccines. Specifically, we will explore programmable DNA-nanostructures to assemble nicotine and other immunogenic components to enhance the immunogenicity and efficacy of the vaccines. To accomplish this, we will combine expertise from immunology, organic and DNA-structural chemistry, bioinformatics, and the pharmacology of nicotine addiction and behaviors. We will implement a three- phase plan, which is staggered and iterative between vaccine construction and assessment, and between immunogenicity and efficacy tests, as well as being guided by several quantitative benchmarks. Our objective is to identify 1 to 2 lead candidates by the end of the funding period, possibly advancing them towards an Investigational New Drug (IND) submission. It is conceivable that our approach can be expanded to the development of vaccines against any target of interest, including other drugs of abuse, infectious agents, and tumor antigens, thus providing a new paradigm in vaccine development.
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Rational design and targeted selection of DNA-scaffolded nicotine vaccines
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批准号:8650814
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Effect of VDJ Recombination on Scid B Cell Development
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Effect of VDJ Recombination on Scid B Cell Development
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