The Interplay Between Host Immunity and Clostridium difficile Pathogenesis
The Interplay Between Host Immunity and Clostridium difficile Pathogenesis
批准号:
8026744
负责人:
Gary B Huffnagle
金额:
$44.17万
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:
2010-08-02 至 2015-07-31
关键词:
AddressAreaBacteriaBiological MarkersClinicalClinical TreatmentClostridium difficileComplementDendritic CellsDevelopmentDiseaseEpigenetic ProcessExposure toGeneticGenotypeHistologicHumanImmune responseImmunityIndividualInfectionInflammationInstructionIntegration Host FactorsLaboratoriesLarge IntestineLeadLesionModelingMorbidity - disease rateMusNatureOutcomePathogenesisPathologyPhenotypePseudomembranous ColitisRegulatory T-LymphocyteRelative (related person)ResearchRodentRoleSamplingSerumSeveritiesSeverity of illnessShapesSystemTestingTreatment outcomeVariantclinical phenotypecytokinehuman subjectimprovedinsightmicrobial hostmolecular markermortalitymouse modelneutrophilpathogenpreventresearch studyresponse
中文摘要
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英文摘要
PROJECT SUMMARY (See instructions):
Clostridium difficile infection (CDI) is a significant cause of morbidity and mortality. Disease related to CDI ranges from asymptomatic colonization to mild diarrheal disease to severe pseudomembranous colifis. Despite the extensive characterizafion of the histologic lesions associated with C. difficile infection, virtually nothing is known mechanistically about the contribution of host factors in disease. It is likely that some of the clinical differences encountered in infected individuals are due to variafion in host response to colonization with C. difficile. We hypothesize that variation in the host innate and adaptive responses for C. difficile are in part responsible for the different clinical phenotypes that are seen in the setting of CDI. Furthermore, we speculate that these variable responses reflect underiying genetic and possibly epigenetic differences in the host. To address these hypotheses we propose the following specific aims: In the first aim we will characterize the innate and adaptive immune response to C. difficile colonization and determine the role of this response in determining the disease manifestations. In the second aim we will identify serum fecal biomarkers and epigenetic changes that correlate distinct clinical outcomes. This aim will examine samples obtained from the Project area #1 for this purpose. The third aim will examine the interaction between host genetics/immune response and C. difficile genotype in the pathogenesis of disease. Mice with defined differences in host response will be challenged with C. difficile strains generated and characterized from the human studies in Project area #1. This will provide an examinafion ofthe relative contribution of host and pathogen factors in disease.
These experiments will increase our understanding ofthe host and microbial mechanisms of C.
d/Wc/Ve-induced colonic inflammation vs. asymptomatic colonization and identify biomarkers that can be used to improve clinical treatments and outcomes.
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