IMMUNE MODULATION OF THE FETUS BY INTRA-AMNIOTIC IL-1
IMMUNE MODULATION OF THE FETUS BY INTRA-AMNIOTIC IL-1
批准号:
8357355
负责人:
CLAIRE A CHOUGNET
金额:
$5.04万
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-05-01 至 2012-04-30
关键词:
Bronchopulmonary DysplasiaCaliforniaComplicationDevelopmentDiagnosisFetusFundingGrantInfantInterleukin-1Interleukin-17LungLung InflammationNational Center for Research ResourcesNeurodevelopmental DeficitNewborn InfantPremature InfantPrimatesPrincipal InvestigatorResearchResearch InfrastructureResourcesSourceUnited States National Institutes of HealthVery Low Birth Weight Infantcostdisabilityimmunoregulation
中文摘要
这个子项目是许多利用资源的研究子项目之一
由NIH/NCRR资助的中心拨款提供。子项目的主要支持
而子项目的主要调查员可能是由其他来源提供的,
包括其它NIH来源。 列出的子项目总成本可能
代表子项目使用的中心基础设施的估计数量,
而不是由NCRR赠款提供给子项目或子项目工作人员的直接资金。
支气管肺发育不良(BPD)是极低出生体重(VLBW)新生儿最常见的并发症,在美国约有15,000名婴儿被诊断出患有BPD,导致终身肺残疾,并与神经发育缺陷相关。IL-1/IL-17轴已被证明是参与这些VLWB早产儿肺部炎症发展的关键机制。
英文摘要
This subproject is one of many research subprojects utilizing the resources
provided by a Center grant funded by NIH/NCRR. Primary support for the subproject
and the subproject's principal investigator may have been provided by other sources,
including other NIH sources. The Total Cost listed for the subproject likely
represents the estimated amount of Center infrastructure utilized by the subproject,
not direct funding provided by the NCRR grant to the subproject or subproject staff.
Bronchopulmonary dysplasia (BPD) is the most common complication in very low birth weight (VLBW) newborns, and is diagnosed in about 15,000 infants in the U.S. BPD results in lifelong pulmonary disabilities and is associated with neurodevelopmental deficits. The IL-1/IL-17 axis has been shown to be a critical mechanism involved in the development of lung inflammation in these VLWB preterm babies.
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