T cell subsets in inflammatory bowel disease
炎症性肠病中的 T 细胞亚群
基本信息
- 批准号:10569030
- 负责人:
- 金额:--
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2022
- 资助国家:美国
- 起止时间:2022-04-01 至 2026-03-31
- 项目状态:未结题
- 来源:
- 关键词:AbscessAddressAffectAutoimmune DiseasesBiological Response Modifier TherapyCD8-Positive T-LymphocytesCRISPR/Cas technologyCategoriesCell modelCellsChronicCrohn&aposs diseaseCytometryDevelopmentDiseaseDisease remissionExhibitsFailureFinancial HardshipFistulaFunctional disorderGastrointestinal tract structureGeneticHealthHumanIL17 geneImmuneImmune systemImmunityIndividualInflammationInflammatoryInflammatory Bowel DiseasesIntestinal DiseasesIntestinesKnock-outKnowledgeLocationLongevityMediatingMemoryModelingMolecularMorbidity - disease rateMultiple SclerosisNaturePathogenesisPathogenicityPatientsPharmaceutical PreparationsPharmacotherapyPlayProcessProtein AnalysisRectumRefractoryRegulationRelapseReportingRheumatoid ArthritisRiskRoleSystemic Lupus ErythematosusT cell differentiationT memory cellT-Lymphocyte SubsetsThyroiditisTimeTissuesUlcerative ColitisUnited StatesVeteransVeterans Health AdministrationWorkbase editingbiomarker identificationcytokinegut inflammationimmunogenicitymilitary veteranmortalitymouse modelnew therapeutic targetnovel therapeutic interventionpathogenic microbeprotein profilingrectalsingle-cell RNA sequencingtranscription factortranscriptomic profiling
项目摘要
Summary
The inflammatory bowel diseases (IBD) are chronic, incurable conditions that contribute to significant morbidity
and mortality in the Veteran population. Current therapies are effective long-term in only ~25% of patients with
IBD, suggesting that as yet unknown immune cell subsets may be involved in the initial development and
relapsing-remitting nature of IBD. We propose to elucidate T cell subsets that may play a role in the
pathophysiology of IBD; this work may ultimately lead to new therapeutic targets for IBD.
总结
炎症性肠病(IBD)是一种慢性、不可治愈的疾病,
以及退伍军人的死亡率目前的治疗方法仅对约25%的患者长期有效,
IBD,这表明迄今未知的免疫细胞亚群可能参与了最初的发展,
IBD的复发-缓解性质。我们建议阐明T细胞亚群,可能发挥作用,在
IBD的病理生理学;这项工作可能最终导致IBD的新治疗靶点。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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John T Chang其他文献
Erratum: Epigenetic landscapes reveal transcription factors that regulate CD8+ T cell differentiation
勘误表:表观遗传景观揭示了调节 CD8 T 细胞分化的转录因子
- DOI:
- 发表时间:
2017 - 期刊:
- 影响因子:30.5
- 作者:
Bingfei Yu;Kai Zhang;J. Milner;Clara Toma;Runqiang Chen;James P Scott;Renata M Pereira;Shane Crotty;John T Chang;M. Pipkin;Wei Wang;A. Goldrath - 通讯作者:
A. Goldrath
Drug Insight: antagonists of tumor-necrosis factor-α in the treatment of inflammatory bowel disease
药物洞察:肿瘤坏死因子-α拮抗剂在炎症性肠病治疗中的应用
- DOI:
10.1038/ncpgasthep0447 - 发表时间:
2006-04-01 - 期刊:
- 影响因子:51.000
- 作者:
John T Chang;Gary R Lichtenstein - 通讯作者:
Gary R Lichtenstein
John T Chang的其他文献
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{{ truncateString('John T Chang', 18)}}的其他基金
Using single-cell RNA-seq to interrogate host immunity to pathogens
使用单细胞 RNA-seq 探究宿主对病原体的免疫力
- 批准号:
9367846 - 财政年份:2017
- 资助金额:
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