The Study of Families with Heritable Crohn's Disease to Support Rational Design of Microbiodata-Based Therapies
The Study of Families with Heritable Crohn's Disease to Support Rational Design of Microbiodata-Based Therapies
批准号:
10358898
负责人:
LEA A CHEN
金额:
$21.82万
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
已结题
起止时间:
2021-02-24 至 2024-12-31
关键词:
AddressAffectAnimal ModelAnti-Inflammatory AgentsBehaviorBiologicalCharacteristicsCluster AnalysisCouplingCrohn&aposs diseaseDataDevelopmentDimensionsDiseaseEnvironmentEnvironmental ExposureEnvironmental Risk FactorEtiologyExposure toFamilyFamily StudyFamily memberFunctional disorderFutureGenesGenetic DeterminismGenetic Predisposition to DiseaseGenetic RiskGenotypeGerm-FreeGoalsHeritabilityHistologyHumanHuman MicrobiomeImmune responseImmunosuppressionIncidenceIndividualInfectionInflammatory Bowel DiseasesInterleukin-10InterventionIntestinesLeadLeftLeukocyte L1 Antigen ComplexMalignant NeoplasmsMapsMeasuresMediatingMentorsMicrobeModelingMultiomic DataMusOnset of illnessOrganismOutcomePathogenesisPathogenicityPathway interactionsPhenotypePopulationPredisposing FactorPublishingResearch PersonnelRiskRoleSamplingSeverity of illnessSignal TransductionSystemTestingTherapeuticTissuesTrainingTransplantationcandidate identificationcareerclinical careclinical developmentcytokinedisorder riskdisorder subtypeexperiencefecal transplantationgut bacteriagut inflammationgut microbesgut microbiomehigh risk populationinsightmetabolomemetabolomicsmicrobialmicrobial signaturemicrobiomemicrobiome compositionmicrobiome researchmicrobiotamouse modelpermissivenesspersonalized medicinepolygenic risk scorepreventrational designrisk varianttranscriptomicstranslational scientist
中文摘要
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英文摘要
Project Summary/Abstract
The cause of Crohn's disease (CD) is believed to be rooted in the interactions between genetic susceptibilities
and exposures to environmental factors, such as specific gut microbes. Unfortunately, the complexity of these
interactions makes it difficult to understand what portion of CD risk is modifiable, and particularly whether gut
microbiome compositions can be altered to overcome one's underlying and fixed genetic predisposition. This
proposal will address whether individuals at high genetic risk for CD, but who never develop disease, harbor
characteristic gut microbial signatures that signal protection from CD. It will furthermore address whether
protective microbiomes can be transferred to diminish, delay, or prevent CD activity in others. Aim 1 will entail
the study of multigenerational families with multiplex CD – with the rationale that families, sharing common
living environments, meals, and behaviors, will minimize common confounders of human microbiome studies.
Individuals will be stratified by a polygenic risk score to better identify those at highest genetic risk but remain
disease-free and who are hypothesized as being most likely to harbor intestinal microbiomic and metabolomic
signatures that characterize disease protection. In Aim 2, select fecal biospecimens (collected in Aim 1)
containing putative protective microbiomes will be transplanted into a germ-free CD mouse model. These mice
will then be characterized by their phenotypic, microbial, metabolomic, and immune responses and assessed
for alterations in disease onset and severity. These studies will provide insights into microbially-mediated
modulators of CD activity; for example, clarifying the yet unknown reason why fecal transplants are very
effective for only a small portion of inflammatory bowel disease cases and why outcomes appear to be heavily
donor-dependent.
Coupling the study of an enriched human population with an animal model, to mechanistically test candidate
protective microbiomes, will streamline the scientific approach and expedite the transition of promising study
findings into clinical care. The scientific proposal and associated training plan will furthermore prepare the PI,
so that she will be well-equipped to lead future studies of host-microbe dynamics in inflammatory bowel
disease as an independent translational investigator.
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The Study of Families with Heritable Crohn's Disease to Support Rational Design of Microbiodata-Based Therapies
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批准号:10382471
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项目类别:
-
资助金额:$21.9万
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财政年份:2020
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负责人:LEA A CHEN
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依托单位:
The Study of Families with Heritable Crohn's Disease to Support Rational Design of Microbiodata-Based Therapies
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批准号:10359937
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项目类别:
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资助金额:$21.99万
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财政年份:2020
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负责人:LEA A CHEN
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依托单位:
The Study of Families with Heritable Crohn's Disease to Support Rational Design of Microbiota-based Therapies
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批准号:9892576
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项目类别:
-
资助金额:$19.74万
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财政年份:2020
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负责人:LEA A CHEN
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依托单位:
海外基金