CD40-Induced TCR Revision: A Mechanism for Autoimmunity
CD40-Induced TCR Revision: A Mechanism for Autoimmunity
批准号:
7655274
负责人:
David H. Wagner
金额:
$27.84万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-08-01 至 2012-07-31
关键词:
AddressAffectAgeAntigensAutoimmune DiseasesAutoimmune ProcessAutoimmunityBiological AssayCD40 LigandCellsDevelopmentDiabetes MellitusDiseaseDisease modelEventGenerationsGenetic RecombinationGoalsGrantHaplotypesHumanHyperglycemiaIn VitroInbred NOD MiceInsulin-Dependent Diabetes MellitusKineticsLaboratoriesLightManuscriptsMediatingMemoryModelingMouse StrainsMusNon-Insulin-Dependent Diabetes MellitusOvalbuminPancreasPeripheralPhenotypePlayPopulationPreventionProcessReceptor CellRiskRoleSourceSpecificitySystemT-Cell ActivationT-Cell Immunologic SpecificityT-Cell ReceptorT-LymphocyteT-Lymphocyte SubsetsTNFRSF5 geneTNFSF5 geneTestingTherapeuticTransgenic MiceTranslatingdesignhuman diseasein vivoin vivo Modelinsulin dependent diabetes mellitus onsetnon-diabeticpreventreceptor expressionresearch studyresponse
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The goals of this application are to address the development of CD40+ T cells, the role that CD40 plays in T cell receptor (TCR) revision and how induced TCR revision impacts autoimmunity. CD40 has a direct role in autoimmune diseases including type 1 diabetes (T1D). We discovered that a unique subset of effector T cells, described as CD4loCD40+, are highly pathogenic in T1 D. CD40 is present on diabetogenic T cell clones and primary CD4loCD40+ T cells expand concurrently with insulitis in NOD mice. Importantly, CD4loCD40+ T cells readily transfer T1D to NOD.scid recipients. Mechanistically, CD40 induces the RAG1/RAG2 recombination machinery in T cells. Following that induction, TCR revision, induced alteration of TCR expression, occurs. Some revised primary T cells were found to be highly pathogenic. However, CD40 induced TCR revision could serve as a functional tolerance mechanism of established diabetogenic T cell clones. Specifically, CD40 engaging the diabetogenic T cell clone BDC2.5 severely ablated disease transfer ability of the clone. We showed that blocking CD40 - CD154 (the ligand for CD40) interaction in NOD mice at 3-weeks of age prevents not only T1D onset, but prevents expansion of CD4loCD40+, autoaggressive cells. In this application we will explore how CD40 affects the unique T cell population. Our hypothesis is that TCR revision directly impacts T cell tolerance. Specific Aim #1: Do CD4loCD40+ T cells comprise a unique T cell subset or represent a transient activation state within T cells? If CD40 is induced on T cells are there differences in those T cells compared to the intrinsic CD40 T cell subset? We plan experiments to address this central concern. Specific Aim #2: How does CD40 engagement affect TCR revision in CD4loCD40+ T cells? Are there differences in response to CD40 engagement between autoimmune and non-autoimmune conditions? We will explore RAG1 and RAG2 induction, kinetics of TCR revision and how different sources of CD154 in autoimmune versus non-autoimmune mice affect this process. Specific Aim #3: How does CD40 engagement affect T cell antigen specificity? We will explore how induced TCR revision affects T cell antigen specificity using in vitro and in vivo models. These proposed studies address not only the development of potential autoaggressive T cells but will provide important information as to whether induced TCR revision is pathogenic or tolerogenic.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Discovering the Mechanism of Action of a peptide drug, OPT101, that targets CD40 mediated inflammation in type 1 diabetes
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批准号:10345075
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项目类别:
-
资助金额:$44.01万
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财政年份:2022
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负责人:David H. Wagner
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依托单位:
Discovering the Mechanism of Action of a peptide drug, OPT101, that targets CD40 mediated inflammation in type 1 diabetes
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批准号:10589075
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项目类别:
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资助金额:$44.01万
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财政年份:2022
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负责人:David H. Wagner
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依托单位:
A unique approach to control the CD40/CD154 inflammatory axis in type 1 diabetes
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批准号:8508619
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项目类别:
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资助金额:$18.16万
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财政年份:2013
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负责人:David H. Wagner
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依托单位:
A unique approach to control the CD40/CD154 inflammatory axis in type 1 diabetes
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批准号:8716665
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项目类别:
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资助金额:$23.26万
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财政年份:2013
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负责人:David H. Wagner
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依托单位:
CD40-Induced TCR Revision: A Mechanism for Autoimmunity
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批准号:8000721
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项目类别:
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资助金额:$15.46万
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财政年份:2010
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负责人:David H. Wagner
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依托单位:
CD40-Induced TCR Revision: A Mechanism for Autoimmunity
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批准号:8113290
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项目类别:
-
资助金额:$27.29万
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财政年份:2007
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负责人:David H. Wagner
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依托单位:
CD40-Induced TCR Revision: A Mechanism for Autoimmunity
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批准号:7771490
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项目类别:
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资助金额:$0.15万
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财政年份:2007
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负责人:David H. Wagner
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依托单位:
CD40-Induced TCR Revision: A Mechanism for Autoimmunity
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批准号:7313568
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项目类别:
-
资助金额:$28.41万
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财政年份:2007
-
负责人:David H. Wagner
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依托单位:
CD40-Induced TCR Revision: A Mechanism for Autoimmunity
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批准号:7473258
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项目类别:
-
资助金额:$27.84万
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财政年份:2007
-
负责人:David H. Wagner
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依托单位:
海外基金