Novel vaccines for otitis media
Novel vaccines for otitis media
批准号:
7933803
负责人:
Elaine I Tuomanen
金额:
$40.08万
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:
2009-09-17 至 2012-08-31
关键词:
AcuteAddressAdverse effectsAnimal ModelAnimalsAntibiotic TherapyAntibioticsAntibodiesAntibody FormationApplications GrantsAreaAttentionAttenuatedAttenuated Live Virus VaccineB-LymphocytesCD4 Positive T LymphocytesCellsChildChildhoodClinicClinicalClinical DataClinical ResearchConjugate VaccinesDataDevelopmentDiseaseDrug resistanceEconomic BurdenEffectivenessFerretsFundingGrantHelper-Inducer T-LymphocyteImmuneImmune responseImmunobiologyImmunoglobulin Class SwitchingImmunologyInfectionInfection preventionKnowledgeLifeLinkMediatingMedicalMembrane ProteinsMethodsModelingMucosal Immune ResponsesMucosal ImmunityMusOtitis MediaPatient observationPhysiciansPneumococcal InfectionsPneumococcal vaccinePneumoniaPopulationPreventionPrevnarRecommendationRecoveryRelative (related person)ResistanceRisk FactorsRunningSerotypingStreptococcus pneumoniaeT cell responseTestingVaccinatedVaccinationVaccinesVisitWorkcapsulecostmeetingsnovelnovel vaccinespre-clinicalpreventprotective efficacypublic health relevanceresponsestemvaccination strategyvaccine candidate
中文摘要
描述(申请人提供):这项建议符合临床研究中两个主要挑战领域的要求,即“预防中耳炎”(04-DC101)和“发展新方法和解决粘膜免疫学的关键问题”(04-AI-101)。
肺炎链球菌引起的中耳炎给儿童带来了巨大的医疗负担。虽然肺炎球菌多价结合疫苗Prevnar的问世总体上减轻了肺炎球菌疾病的负担,但事实证明,次优的粘膜免疫反应在获得有效保护方面存在问题。即使接种了疫苗,急性中耳炎也是儿科医生就诊的主要原因,也是给幼儿开出的大部分抗生素的原因。这强调了开发新的疫苗接种策略和更好地了解宿主粘膜免疫的重要性。为此,鼻腔接种作为一种替代策略最近受到了相当大的关注,因为它在诱导强大的粘膜免疫反应方面具有潜在的有效性。我们建议使用新描述的强大的动物模型来评估两种新的针对中耳炎的新型减毒肺炎球菌活疫苗的免疫应答和保护效果。这些数据有望扩大我们对中耳炎粘膜免疫的了解,并为将新型疫苗推向临床提供有用的临床前数据。
公共卫生相关性:由肺炎链球菌引起的中耳炎是儿童的重大医疗负担。虽然肺炎球菌多价结合疫苗Prevnar的问世总体上减轻了肺炎球菌疾病的负担,但事实证明,次优的粘膜免疫反应在获得有效保护方面存在问题。即使接种了疫苗,急性中耳炎也是儿科医生就诊的主要原因,也是给幼儿开出的大部分抗生素的原因。这强调了
开发新的疫苗接种策略和更好地了解宿主粘膜免疫的重要性。为此,鼻腔接种作为一种替代策略最近受到了相当大的关注,因为它在诱导强大的粘膜免疫反应方面具有潜在的有效性。我们建议评估两种新的针对中耳炎的新型减毒肺炎球菌活疫苗的免疫应答和保护效果。
健壮的动物模型。这些数据有望扩大我们对中耳炎粘膜免疫的了解,并为将新型疫苗推向临床提供有用的临床前数据。
英文摘要
DESCRIPTION (provided by applicant): This proposal meets the requirements of two major Challenge Areas within Clinical Research, "Prevention of otitis media" (04-DC101), and "Develop novel methods and address key questions in mucosal immunology" (04-AI-101).
Otitis media caused by Streptococcus pneumoniae represents a significant medical burden in children. While the advent of the pneumococcal polyvalent conjugate vaccine Prevnar has decreased the burden of pneumococcal disease overall, the suboptimal mucosal immune response has proved problematic in eliciting effective protection. Even with vaccination, acute otitis media is the leading cause of pediatric physician visits and is responsible for a majority of the antibiotics prescribed to young children. This underscores the importance of development of new vaccination strategies and a greater understanding of host mucosal immunity. To this end, intranasal vaccination has recently gained considerable attention as an alternative strategy due to potential effectiveness at inducing a robust mucosal immune response. We propose to evaluate the immune responses and protective efficacy of two novel live, attenuated pneumococcal vaccines against otitis media using newly described, robust animal models. These data are expected to expand our knowledge of mucosal immunity to otitis media and provide pre-clinical data useful for advancing novel vaccines to the clinic.
PUBLIC HEALTH RELEVANCE: Otitis media caused by Streptococcus pneumoniae represents a significant medical burden in children. While the advent of the pneumococcal polyvalent conjugate vaccine Prevnar has decreased the burden of pneumococcal disease overall, the suboptimal mucosal immune response has proved problematic in eliciting effective protection. Even with vaccination, acute otitis media is the leading cause of pediatric physician visits and is responsible for a majority of the antibiotics prescribed to young children. This underscores
the importance of development of new vaccination strategies and a greater understanding of host mucosal immunity. To this end, intranasal vaccination has recently gained considerable attention as an alternative strategy due to potential effectiveness at inducing a robust mucosal immune response. We propose to evaluate the immune responses and protective efficacy of two novel live, attenuated pneumococcal vaccines against otitis media using newly described,
robust animal models. These data are expected to expand our knowledge of mucosal immunity to otitis media and provide pre-clinical data useful for advancing novel vaccines to the clinic.
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会议论文
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Pathogenesis and Molecular Epidemiology of Pneumococcal Infection in Sickle Cell
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海外基金