Skin Vaccination Against Influenza in the Young And Aged
Skin Vaccination Against Influenza in the Young And Aged
批准号:
9210049
负责人:
RICHARD W COMPANS
金额:
$67.49万
依托单位:
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:
2015-02-06 至 2020-01-31
关键词:
AdultAnimal ModelAnimalsAntigen-Presenting CellsAntigensAttenuated Live Virus VaccineB-LymphocytesCaviaCellsCessation of lifeCharacteristicsChildDataElderlyExhibitsFDA approvedGoalsHospitalizationHumanImmuneImmune responseImmune systemImmunityImmunizationImmunologicsIndividualInfectionInflammatoryInfluenzaInfluenza A Virus, H1N1 SubtypeInfluenza A Virus, H7N9 SubtypeInfluenza vaccinationInnate Immune SystemIntramuscularMorbidity - disease rateMusPainlessPhenotypePopulationPopulation GroupPopulation HeterogeneityPublic HealthRecruitment ActivityResearchRiskRoleRouteSignal TransductionSiteSkinSkin AgingSubunit VaccinesSupport GroupsT cell responseTechnologyUp-RegulationVaccinationVaccine ResearchVaccinesVirusVirus Diseasesadaptive immune responseagedaging populationchemokinecytokinedesignexperienceglobal healthgroup supporthigh riskhigh risk populationimmunogenicityimmunoregulationimmunosenescenceimprovedinfluenza outbreakinfluenza virus vaccineinfluenzavirusinsightmortalitymouse modelnonhuman primatepandemic diseasepreventpublic health relevancerelative effectivenesssenescenceuptakevaccination strategyvaccine deliveryvaccine developmentvaccine efficacy
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): It is widely recognized that the young and elderly represent two population groups at high risk from influenza virus infection. Morbidity and mortality from influenza-related illness and secondary complications are highest in these groups. Although current influenza vaccines are relatively effective in eliciting protective immune
responses in adults, they only confer limited protective immunity in the young and aged. The reasons for the reduced efficacy in these groups could be a result of various factors including reduced potency/immunogenicity of split and subunit influenza vaccines, the lack of prior exposure and immaturity of the immune system observed in young individuals and the immunosenescence observed in the elderly. The current intramuscular route used to administer these vaccines may also be less effective for antigen uptake and presentation due to the reduced interaction with MHC II immune cells, thus limiting the magnitude of the immune responses. In order to improve vaccine efficacy in these high risk groups we propose to determine if delivery of influenza vaccine through the skin of the young and aged can confer improved immune responses and protection when compared to intramuscular immunization. We plan to build on our preliminary data and previous studies, and take advantage of our extensive experience with different types of microneedle designs and technologies and unique animal models to successfully complete this project. We are motivated by our findings that skin microneedle delivery of existing FDA-approved influenza vaccine formulations can enhance the immune responses in animal models and confer improved protection when compared to intramuscular immunization in the young and aged. Thus, our research has the potential to suggest new vaccination approaches and immunization strategies that will impact and improve public health globally.
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Skin Vaccination Against Influenza in the Young And Aged
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海外基金