Innate immune response to bacterial flagellins
Innate immune response to bacterial flagellins
批准号:
8890740
负责人:
STEPHEN J MCSORLEY
金额:
$38.16万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-05-16 至 2017-07-31
关键词:
Adaptor Signaling ProteinAdjuvantAnimalsAntibodiesAntigen TargetingAwardB-LymphocytesBacteriaBacterial InfectionsBacterial ProteinsBasic ScienceBindingBiological AssayCCR6 geneCD4 Positive T LymphocytesCaspaseCell Surface ReceptorsCholeraComplexDataDendritic CellsDendritic cell activationDevelopmentDiseaseEnterobacteriaceaeFlagellaFlagellinFundingGenesGoalsGrantHistocompatibility Antigens Class IIHumanImmuneImmune responseImmune systemImmunityImmunizationIn VitroInfectionInflammatoryInflammatory Bowel DiseasesInflammatory ResponseInflammatory disease of the intestineIntestinesLaboratoriesLigandsLigationMHC Class II GenesMastigophoraMicrobeModelingMonitorMyelogenousNatural ImmunityPathway interactionsPatientsPeptidesPhosphorylationPlantsPreventionProcessProductionProtein Tyrosine KinaseProteinsReceptors, Antigen, B-CellRecruitment ActivityReportingRoleShapesSignal PathwaySignal TransductionSpecificitySystemT cell responseT-Cell ReceptorT-LymphocyteTechnologyTestingToll-Like Receptor 5Translational ResearchTyphoid FeverVaccine AdjuvantVaccinesadaptive immunityarmcytokineimmunogenicin vivonovel vaccinespathogenreceptorresponsescavenger receptortargeted treatmenttraffickingvaccine development
中文摘要
描述(由申请人提供):鞭毛菌是人类的常见病原体,可引起许多重要疾病,包括伤寒和霍乱。鞭毛蛋白是许多肠道细菌感染期间以及炎症性肠道疾病患者免疫反应的主要靶抗原。因此,了解鞭毛蛋白激活先天性和适应性免疫反应的非凡能力对于肠道感染疫苗和佐剂的转化研究以及预防炎症性疾病的基础研究至关重要。
利用为期2年的ARRA资助,我们发现先天受体TLR5对于T细胞对鞭毛蛋白的强烈反应的发展至关重要,但这需要一种以前未被研究过的非常规信号通路。此外,我们现在已经开发了敏感的体外和体内检测方法来监测鞭毛蛋白特异性
树突状细胞的T细胞反应。在这次更新申请中,我们建议在ARRA资助下完成的成功研究的基础上,继续研究TLR5在鞭毛蛋白特异性免疫发展中的作用。
该分项目的具体目标是:目标1。检查TLR5下游的一个新的信号通路,以检验DCs激活鞭毛蛋白特异性T细胞所需的自噬和自噬通路组分的假设。目标二。具体目标2。检查肠道DC亚群激活鞭毛蛋白特异性T细胞的能力,以检验CCR 6 + PP DC负责对鞭毛病原体的适应性免疫反应的假设。我们的初步数据描述了最先进的技术的发展,以检查鞭毛蛋白特异性T细胞的反应,在体外和体内。我们的总体假设是TLR5作为肠道DC上的清道夫受体发挥功能,将T细胞反应集中在鞭毛蛋白上。
英文摘要
DESCRIPTION (provided by applicant): Flagellated bacteria are common pathogens of humans and cause many important diseases including typhoid and cholera. Flagellins are dominant target antigens of the immune response during many intestinal bacterial infections and also in patients suffering from inflammatory bowel disease. Understanding the extraordinary ability of flagellins to activate innate and adaptive immune responses is therefore of critical importance for translational research on vaccines and adjuvants for intestinal infections and for basic research on the prevention of inflammatory disease.
Using 2-year ARRA funding, we have found that the innate receptor TLR5 is essential for the development of a robust T cell response to flagellin, but that this requires an unconventional signaling pathway that has not previously been examined. In addition, we have now developed sensitive in vitro and in vivo assays to monitor the activation of flagellin-specific
T cell responses by dendritic cells. In this renewal application we propose to build upon our successful studies completed with ARRA funding and continue studying the role of TLR5 in the development of flagellin-specific immunity.
The specific aims of this sub-project are: Aim 1. Examine a new signaling pathway downstream of TLR5 to test the hypothesis that components of CLR and autophagic pathways are required by DCs to activate flagellin-specific T cells. Aim 2. Specific Aim 2. Examine the ability of intestinal DC subsets to activate flagellin-specific T cells, to test the hypothesis tha CCR6+ PP DCs are responsible for adaptive immune responses to flagellated pathogens. Our preliminary data describe the development of state-of-the-art technology to examine flagellin- specific T cell responses in vitro and in vivo. Our overall hypothesis is that TLR5 functions as a scavenger receptor on intestinal DCs to focus T cell responses onto flagellin.
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