Immune Profile and Network Analysis of Malaria Infection and Vaccination
Immune Profile and Network Analysis of Malaria Infection and Vaccination
批准号:
9129262
负责人:
Margaret Juliana McElrath
金额:
$24.63万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-09-29 至 2017-08-31
关键词:
AdultAffectAfricanAntibody ResponseAntigensAntimalarialsBiometryBreedingCharacteristicsChildClinicalClinical TrialsCommunitiesCountryDNADataDevelopmentFoundationsGenetic TranscriptionGoalsGrantImmuneImmune responseImmune systemImmunityImmunizationImmunologyInfectionInformaticsInstitutionIntegration Host FactorsLaboratoriesLeadLeukocytesLifeMalariaMalaria VaccinesMethodologyMolecular ProfilingNatural ImmunityParasitesPathway AnalysisPhasePhenotypePlasmodium falciparumPopulationPopulation StudyProcessResearchResearch DesignResearch PersonnelSamplingSpecificitySterilityStrategic PlanningSystems BiologyTechnologyTimeVaccinationVaccinescell typechemokinecytokinedesignimmune functionimprovedinsightprogramsresponsetrial designvaccine developmentvaccine efficacyvaccine trial
中文摘要
描述(由申请人提供):这是疟疾疫苗的一个合适的时机(开发疫苗效力的第一个迹象,并承诺在正在进行的试验中非常有效的疫苗,计划在明年进行,并准备在赠款期间进入1/2a期临床试验。一个由来自强大机构并具有疟疾、免疫学、系统生物学、疫苗和生物统计学互补专长的专家组成的联盟已经聚集起来,使用现有的试验样本,以详细描述抗疟免疫应答及其与免疫保护的关系。这一机会吸引了正在进行疫苗试验和将提供临床样品的人的热情参与。这些试验的设计支持全面的免疫分析和网络分析评估。将在接种疫苗和攻毒或自然感染之前和之后从研究人群中采集样本,这些人群包括从未患过疟疾的成人至生活在流行地区的儿童和成人。恶性疟原虫的范围从充分表征的临床分离株(例如NF 54)到几个非洲国家的生物多样性自然种群。该项目将使用广泛的最佳方法来表征广泛的免疫反应和免疫细胞类型。这包括对疟疾特异性白细胞表型、细胞因子和趋化因子谱、抗体反应以及转录和宿主DNA分析的多参数评估。这被设计为生成免疫应答的概况,其可以在系统生物学方法中与免疫状态和机制相关,并识别与免疫保护相关的功能网络。该研究旨在深入了解疟疾的保护性免疫机制,以改进抗疟疾疫苗,并为改进疫苗开发奠定基础,以便与社区共享。
相关性:一个拥有互补专业知识的研究人员联盟,跨越了广泛的高端实验室和信息技术,已经联合起来全面描述了对疟疾感染的免疫反应和免疫力的发展。该项目的总体目标是阐明疟疾免疫保护机制,以加速开发广泛有效的疟疾疫苗,并推动疫苗开发的总体进程。
英文摘要
DESCRIPTION (provided by applicant): It Is an opportune time for malaria vaccine (development with the first indication of vaccine efficacy and the promise of very effective vaccines in trials that are underway, planned for the coming year, and poised to enter phase 1/2a clinical trials during the grant period. A consortium of committed experts from strong institutions and with complementary expertise in malaria, immunology, systems biology, vaccines, and biostatistics has assembled to use the available trial samples in order to characterize in detail antimalarial immune responses and their relationship to immune protection. This opportunity attracted the enthusiastic participation of those who are conducting vaccine trials and who will provide the clinical samples. The design of these trials supports comprehensive immune profiling and network analysis assessment. Samples will be obtained prior to and following vaccination and challenge or natural infection from study populations that span malaria-naive adults to children and adults living in endemic regions. The P. falciparum parasites range from well characterized clinical isolates (e.g. NF54) to biodiverse natural populations in several African countries. The project will use a wide range of best-of-breed methodologies to characterize a wide range of immune responses and immune cell types. This includes multi-parametric assessments of malaria specific leukocyte phenotypes, cytokine and chemokine profiles, antibody responses, and transcriptional and host DNA analyses. This is designed to generate a profiles of immune responses that can in a systems biology approach be correlated with immune status and mechanisms and identify functional networks associated with immune protection. The study is designed to provide insight into protective immune mechanisms to malaria in order to improve anti-malarial vaccines and also to lay a foundation for improved vaccine development in general that can be shared with the community.
RELEVANCE: A consortium of investigators with complementary expertise that span a wide range of high-end laboratory and informatic technologies have joined forces to comprehensively profile immune responses to malaria infection and the development of immunity. The overall goal of this project is to elucidate the mechanisms of immune protection to malaria in order to accelerate development of a broadly effective malaria vaccine and to advance the process of vaccine development in general.
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