Microbiome and immunosenescence of T cells repertoire
Microbiome and immunosenescence of T cells repertoire
批准号:
10417234
负责人:
LESZEK IGNATOWICZ
金额:
$39.0万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
未结题
起止时间:
2020-09-30 至 2025-04-30
关键词:
AgeAgingAnti-Inflammatory AgentsAntigensBacteriaCD4 Positive T LymphocytesCellsChronicCollectionDataDiseaseEcosystemElderlyEpitopesEquilibriumFOXP3 geneFunctional disorderGenomeGerm-FreeGoalsGrantHealth BenefitHomeostasisHumanImmuneImmune systemImmunityImmunizationIndividualInflammationInterleukin-10IntestinesLeadLongevityMediatingMetabolismMicrobeMucous MembraneMusOligonucleotidesPatientsPeptidesPlayProbioticsRegulatory T-LymphocyteResearchRoleSpecificityStandardizationSystemT-LymphocyteTNFRSF11B geneTestingTherapeuticTransplantationWorkage relatedbasecommensal microbescytokinedesigndysbiosisenteric pathogengut inflammationgut microbiotaimmunoregulationimmunosenescenceimprovedintestinal homeostasismicrobialmicrobiomemicrobiotamicroorganism antigennovel therapeutic interventionpathogen exposurepreventresponsetherapy designtissue injurytranscription factor
中文摘要
肠道微生物群是肠道CD 4 T细胞识别抗原的主要贡献者
细胞这些抗原如何影响CD 4 T细胞免疫衰老及其效应功能
在老年小鼠和人类中的作用尚不清楚。因此,有必要制定一个标准化的
微生物植物群,其具有可管理的大小,并且类似于当
施用于年老体弱的个体将重新平衡他们的肠道内稳态。这个目标
建议是测试这种新的寡克隆小鼠肠上皮细胞集合(寡-MM),
通过系统和基于基因组的方法来概括完整的微生物组,
帮助恢复老化的免疫系统。特别是,我们将研究寡MM微生物群如何
其主要成分Akkermasia municiphila与Cd 4 T细胞相互作用,
这些细胞从细菌中识别的抗原决定簇。在目标1中,我们将研究如何具体
肠梗阻对老年小鼠CD 4 T细胞活化和库影响在我们的目标2
我们将证明A. municiphila衍生抗原诱导幼稚CD 4Foxp 3- T细胞
转化为CD 4Foxp 3 + pT细胞,并显著增加老年小鼠中这些细胞的数量。
我们假设A. municiphila可以改善老年小鼠
耐受肠道微生物群和减少免疫衰老。总的来说,这项研究将有助于
制定基于严格控制的微生物群疗法的新策略,
老年人的炎症
英文摘要
The intestinal microbiota is a major contributor of antigens recognized by intestinal CD4 T
cells. How these antigens influence CD4 T cells immunosenescence and their effector functions
in old mice and humans remains unclear. Therefore, there is a need to develop a standardized
microbial flora that has a manageable size and resembles natural microbiome that when
administered to old, frail individuals will rebalance their intestinal homeostasis. The goal of this
proposal is to test if this new oligoclonal collection of mouse intestinal commensals (oligo-MM),
designed by system and genome-based approaches to recapitulate complete microbiome can
help revitalize an aging immune system. In particular, we will investigate how oligo-MM microbiota
and its main component Akkermasia municiphila interacts with Cd4 T cells and discover immune
epitopes that these cells recognize from this bacteria. In Aim 1 we will investigate how specific
intestinal commensals influence activation and repertoire of CD4 T cells in old mice. In our Aim 2
we will demonstrate that A. municiphila derived antigens induce naïve CD4Foxp3- T cells
conversion to CD4Foxp3+ pTregs and substantially increase the number of these cells in old mice.
We hypothesize that the therapeutic administration of A. municiphila to old mice can improve
tolerance to intestinal microbiota and reduce immunosenescence. Overall this research will help
develop new strategies based on strictly controlled microbiota-based therapies to control intestinal
inflammation in elderly.
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Microbiome and immunosenescence of T cells repertoire
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批准号:10661505
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项目类别:
-
资助金额:$39.0万
-
财政年份:2020
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负责人:LESZEK IGNATOWICZ
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依托单位:
Autoreactive CD4 T cells in healthy mice
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批准号:10170262
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项目类别:
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资助金额:$38.99万
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财政年份:2020
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负责人:LESZEK IGNATOWICZ
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依托单位:
Autoreactive CD4 T cells in healthy mice
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批准号:10621383
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项目类别:
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资助金额:$39.0万
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财政年份:2020
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负责人:LESZEK IGNATOWICZ
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依托单位:
Microbiome and immunosenescence of T cells repertoire
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批准号:10259681
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项目类别:
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资助金额:$38.98万
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财政年份:2020
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负责人:LESZEK IGNATOWICZ
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依托单位:
Autoreactive CD4 T cells in healthy mice
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批准号:10404633
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项目类别:
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资助金额:$39.0万
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财政年份:2020
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负责人:LESZEK IGNATOWICZ
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Diversity of intraepithelial CD8aa T cells that recognize antignes from commensal flora
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批准号:9413085
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项目类别:
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财政年份:2017
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负责人:LESZEK IGNATOWICZ
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依托单位:
Antigenic specificities of intestinal CD4+Foxp3+ T cells.
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批准号:9006761
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项目类别:
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资助金额:$38.0万
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财政年份:2015
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负责人:LESZEK IGNATOWICZ
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依托单位:
Role of CD4+T cells in maintenance of intestinal homeostasis
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批准号:8819131
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项目类别:
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资助金额:$33.01万
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财政年份:2014
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负责人:LESZEK IGNATOWICZ
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依托单位:
Role of CD4+T cells in maintenance of intestinal homeostasis
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批准号:9464232
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项目类别:
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资助金额:$32.95万
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财政年份:2014
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负责人:LESZEK IGNATOWICZ
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依托单位:
Role of CD4+T cells in maintenance of intestinal homeostasis
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批准号:8697992
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项目类别:
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资助金额:$32.79万
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财政年份:2014
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负责人:LESZEK IGNATOWICZ
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依托单位:
Antigenic specificities of intestinal CD4+Foxp3+ T cells.
-
批准号:8894949
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项目类别:
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资助金额:$37.75万
-
财政年份:2014
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负责人:LESZEK IGNATOWICZ
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依托单位:
Ontogeny of natural regulatory T cells.
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批准号:7735488
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项目类别:
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资助金额:$36.75万
-
财政年份:2009
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负责人:LESZEK IGNATOWICZ
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依托单位:
Ontogeny of natural regulatory T cells.
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批准号:7897828
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项目类别:
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资助金额:$36.75万
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财政年份:2009
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负责人:LESZEK IGNATOWICZ
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依托单位:
Visualization of individual Foxp3+ T cells during an onset and progression of aut
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批准号:7888322
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项目类别:
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资助金额:$36.38万
-
财政年份:2008
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负责人:LESZEK IGNATOWICZ
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依托单位:
Visualization of individual Foxp3+ T cells during an onset and progression of aut
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批准号:7646288
-
项目类别:
-
资助金额:$36.75万
-
财政年份:2008
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负责人:LESZEK IGNATOWICZ
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依托单位:
Visualization of individual Foxp3+ T cells during an onset and progression of aut
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批准号:8076741
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项目类别:
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资助金额:$36.02万
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财政年份:2008
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负责人:LESZEK IGNATOWICZ
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依托单位:
Visualization of individual Foxp3+ T cells during an onset and progression of aut
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批准号:7508212
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项目类别:
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资助金额:$36.75万
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财政年份:2008
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负责人:LESZEK IGNATOWICZ
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依托单位:
Visualization of individual Foxp3+ T cells during an onset and progression of aut
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批准号:8274807
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项目类别:
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资助金额:$36.02万
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财政年份:2008
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负责人:LESZEK IGNATOWICZ
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依托单位:
Antigen biased positive selection of CD4+ T cells
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批准号:6640229
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项目类别:
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资助金额:$25.75万
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财政年份:1997
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负责人:LESZEK IGNATOWICZ
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依托单位:
POSITIVE SELECTION BY SINGLE CLASS II MHC/PEPTIDE MOTIFS
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批准号:2669986
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项目类别:
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资助金额:$15.26万
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财政年份:1997
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负责人:LESZEK IGNATOWICZ
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依托单位:
海外基金