Immunity to Cryptosporidium
Immunity to Cryptosporidium
批准号:
10063469
负责人:
CHRISTOPHER A HUNTER
金额:
$73.94万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-12-01 至 2024-11-30
关键词:
AdultAffectAgeAntigensAreaBiological ModelsBiologyBioterrorismC57BL/6 MouseCategoriesCause of DeathCell physiologyCellsChildChild DevelopmentChild MortalityCommunitiesCryptosporidiosisCryptosporidiumDataDefectDendritic CellsDevelopmentDiseaseDisease OutbreaksDropsEngineeringEnterobacteria phage P1 Cre recombinaseEnterocytesEpidemiologyEpithelial CellsEtiologyGene Expression ProfileGene Expression ProfilingGenomicsGrowthHumanHyperplasiaImmuneImmune responseImmune systemImmunityImmunocompetentImmunologicsImmunologistIncidenceIndividualInfectionInflammatoryInterferon Type IIIntestinal DiseasesKnowledgeLeadLifeLiteratureLoxP-flanked alleleMalignant - descriptorMalnutritionMediatingMethodsModelingMolecularMusOrganismOrganoidsParasite ControlParasitesPathway interactionsPlayPopulationPreventionProcessProductionReporterResearchResistanceRoleSTAT1 geneSystemT cell responseT-Cell DevelopmentT-LymphocyteTestingTranslationsVaccinesWateradaptive immunityantimicrobialasexualchlorinationdiarrheal diseaseenteric pathogenexperiencegenetic manipulationin vivointerestmouse modelneglectnovelpathogenpediatric patientspreventprogramsresistance mechanismresponsesingle-cell RNA sequencingtooltransmission processvaccine developmentvillinwaterborne illness
中文摘要
点击翻译按钮获取中文摘要
英文摘要
The apicomplexan parasite Cryptosporidium is a leading cause of death due to diarrheal disease in young
children, particularly in the context of malnutrition, milder infections often result in growth faltering. The
incidence of cryptosporidiosis drops off sharply after the age of two in areas of high transmission, yet in
regions with low transmission adults remain susceptible, as demonstrated by frequent outbreaks in the U.S.
More than 50% of waterborne disease in the U.S. is caused by this parasite which is resistant to water
chlorination and considered a category B potential bioterrorism agent. The epidemiology in children
suggests that initial infection results in long lived protective immunity, a phenomenon also observed in the
context of veterinary cryptosporidiosis. Harnessing this immunity into a vaccine could prevent the disease
and dramatically impact child mortality and development. However, there are significant gaps in our
knowledge of the mechanisms that underlie immunity to Cryptosporidium. We developed a new natural
model of Cryptosporidium infection in immunocompetent C57BL/6 mice that mirrors important aspects of
human cryptosporidiosis and in which host and parasite are genetically tractable. This proposal assembles
an interdisciplinary team of experienced parasite molecular biologist and immunologist to define how the
infected enterocyte senses infection, how it responds to and restricts infection, and how it interacts with
dendritic cells and T cells to trigger and execute a protective immune response. This research will impact
our fundamental understanding of immunity in the gut and drive translation towards prevention of an
important contributor of child mortality.
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会议论文
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