A novel vaccine: botulinum neurotoxin subunit on a viral carrier.
A novel vaccine: botulinum neurotoxin subunit on a viral carrier.
批准号:
8250086
负责人:
Matthias Johannes Schnell
金额:
$81.76万
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:
2012-06-21 至 2015-05-31
关键词:
AdjuvantBacteriaBiological AssayBioterrorismBontoxilysinBotulinum Toxin Type ABotulinum ToxinsBotulismCell LineCell surfaceCellsCenters for Disease Control and Prevention (U.S.)Combined VaccinesComplementary DNAConsent FormsDataDevelopmentEngineeringEnzyme-Linked Immunosorbent AssayFrequenciesGoalsHumanImmune SeraImmune responseImmunizationIn VitroLicensingLifeMeasuresMethodsMilitary PersonnelMusNational Institute of Allergy and Infectious DiseasePhasePlasmidsPreclinical TestingPreparationProceduresProcessProductionProteinsPublic HealthRabies virusRecombinant ProteinsRecombinantsRecordsRecoveryRelative (related person)ResearchResearch Project GrantsSafetySeedsSerotypingSurfaceSystemTechnologyTestingTimeToxic effectToxinToxoidsTranslatingUnited StatesUnited States National Institutes of HealthVaccine ProductionVaccinesViralVirionanalytical methodbiodefensebotulinumbotulinum toxin type Bbotulinum toxin type Ecostemergency service responderhigh riskimmunogenicimprovedin vitro Assayin vivokillingsnext generationnovelnovel vaccinesparticlepositional cloningrabies virus glycoprotein Gresearch studyvaccine developmentvector vaccine
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): According to the NIAID fact sheet on Botulism, "the extreme toxicity of botulinum neurotoxins (BoNT) and the ease of production, transport, and delivery make this an agent of extreme bioterrorism concern." Nonetheless, although there are major vaccine development initiatives ongoing, there currently is no approved Botulinum toxin vaccine available. Advances in Botulinum research have designated the optimal target for vaccine development to be the non-toxic carboxyterminal half of the toxin heavy chain (HC50). In fact, an immediate research goal for NIAID is listed as the development of a HC50 fragment vaccine against botulinum. Building upon the encouraging data from the phase I proof of concept study of this project, the overall phase II project goal is to develop a new, trivalent botulinum vaccine against the most common serotypes A, B and E. Three Aims are proposed for the further development of this novel trivalent BoNT vaccine as follows: Specific Aim 1: Vaccine vector construction and recovery. i) plasmid constructions, ii) demonstration of cell surface expression of the BoNT HC50, and iii) re-recovery of recombinant RVs from cDNA on Vero. Specific Aim 2. Vaccine vector characterization i) purification, inactivation, and in vitro characterization of the RV virions, ii) analysis of mouse immune responses to the vaccine using ELISA, in vitro neutralization assays, and in vivo protection of mice against a single challenge with BoNT or multiple BoNT challenge dependent on the used vaccine(s) for immunization. Specific Aim 3: Development of Pilot Production and Purification Processes. The overall goal of this aim is to translate the production process of our vaccine from a research setting to one suitable for pilot scale vaccine manufacture.
PUBLIC HEALTH RELEVANCE: This research project is directly relevant to public health in that it is directed towards the development of a safe and effective vaccine for Botulinum neurotoxin. Botulinum toxin posesa major bioweapon threat because of its extreme potency andlethality and its ease of production and transport. A current investigational botulinum- toxoid vaccine requires multiple boosts to generate titers that are not very high, highlighting the need for an improved botulinum toxin vaccine. It is unclear if the current Botulinum vaccine protects at
all as indicated by the disclaimer on the CDC vaccine consent form: "..., but other personal protective measures are still required. You should think of personal protective measures as the only protective measure against any of these bacteria (sic) toxins at this time."
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