Functional Interaction Between T-cell and B-cell Immune Pathways in Neuro- inflammatory Disorders
Functional Interaction Between T-cell and B-cell Immune Pathways in Neuro- inflammatory Disorders
批准号:
9332909
负责人:
Robert C Axtell
金额:
$64.61万
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-09-01 至 2018-08-31
关键词:
AddressAffectAnimal ExperimentsAnimal ModelAntibodiesAutoimmune DiseasesAutoimmunityAutologousAutomobile DrivingB Cell ProliferationB-Lymphocyte SubsetsB-LymphocytesBindingBiologicalCD3 AntigensCD4 Positive T LymphocytesCXCL1 geneCXCL13 geneCell CommunicationCell Culture TechniquesCell physiologyCellsCentral Nervous System DiseasesClinicalClinical TrialsCoculture TechniquesCollaborationsComorbidityDNADataDiseaseExperimental Autoimmune EncephalomyelitisFDA approvedGoalsHealthHelper-Inducer T-LymphocyteIL8 geneIL8RB geneImmuneImmune systemIndividualInfiltrationInflammationInflammatoryInterferon-betaInterferonsInterleukin-1 betaInterleukin-17Interleukin-6Knockout MiceLesionLettersLupusMediatingMedicineModelingMultiple SclerosisMusNeuraxisNeurologistNeurologyNeuromyelitis OpticaOptic NerveOptic NeuritisPathologic ProcessesPathway interactionsPatientsPlasmaPlayPropertyProteomicsPublishingReactive Oxygen SpeciesRecruitment ActivityRegulationRelapseResearchRodentRoleSerineSerumSeverity of illnessSorting - Cell MovementSourceSpinalSpinal CordSumSupporting CellSystemic Lupus ErythematosusSystems BiologyT cell differentiationT memory cellT-LymphocyteTestingTimeTissuesTranslationsUniversitiesWhole Bloodaquaporin 4basecell typechemokinecytokinedesignhealthy volunteerhuman subjectinsightinterleukin-23multiple sclerosis patientneutrophilpatient populationpersonalized approachprofessorreconstitutionresponserituximabtraffickingtranscriptome sequencingtranscriptomics
中文摘要
英文摘要
DESCRIPTION (provided by applicant): Neuromyelitis optica (NMO) is a rare but devastating inflammatory disorder of the central nervous system (CNS) that primarily affects the optic nerves and spinal cord. NMO was initially characterized as a subset of multiple sclerosis (MS), but is now considered a distinct disease. Currently, there are no FDA approved therapies for NMO. In fact, many MS therapies, most notably interferon-beta (IFN-β), worsens NMO. The limited therapies for NMO demonstrate that this disease has clear unmet needs in neurology. The goal of this project is to understand the immune pathways that initiate disease activity in NMO. The aims of this proposal will address three connected but distinct issues that will have an impact NMO patients. Aim 1 will determine the immune pathways that are present in patients with MS and NMO. This will be achieved by proteomic analysis of plasma and transcriptomic analysis of CD4+ T-cells and B-cells from patients. Aim 2 will assess the direct interaction between B-cell subsets and T helper cells from NMO and healthy volunteers by utilizing cell culturing techniques. Aim 3 will utilize the animal models we have developed to understand the mechanisms underlying the effects BAFF and APRIL have on T cells, neutrophil and B-cells interactions in neuro- autoimmune disease. The first two aims of this proposal will be a highly translation collaboration between Drs. Axtell, Lessard, Pardo (the director of OMRF's MS Center of Excellence), Anaya (Professor of Medicine at Rosario University, Director of the Autoimmune Diseases Research Center) and the Accelerated Cure Project (ACP). The clinical expertise and large patient population Drs. Pardo, Anaya and the ACP will provide to this project will enable these aims to be accomplished. The third aim utilizes our strength in animal models of neuro-autoimmunity that will give insight into the biological mechanisms behind NMO. The combination of research on human subject and the mechanistic animal experiments outlined in this proposal have the potential to give deep insight into pathological processes that underlie and NMO.
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专著(0)
科研奖励(0)
会议论文
Understanding the roles type I Interferon and TH17 play in Neuromyelitis Optica and other autoimmune diseases.
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批准号:10215451
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项目类别:
-
资助金额:$70.08万
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财政年份:2018
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负责人:Robert C Axtell
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依托单位:
Understanding the roles type I Interferon and TH17 play in Neuromyelitis Optica and other autoimmune diseases.
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批准号:9751758
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项目类别:
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资助金额:$70.08万
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财政年份:2018
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负责人:Robert C Axtell
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依托单位:
Pathogenic B cell and T helper cell interactions in Neuromyelitis Optica
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批准号:10178030
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项目类别:
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资助金额:$42.32万
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财政年份:2017
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负责人:Robert C Axtell
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依托单位:
Pathogenic B cell and T helper cell interactions in Neuromyelitis Optica
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批准号:9216116
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项目类别:
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资助金额:$43.63万
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财政年份:2017
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负责人:Robert C Axtell
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依托单位:
Molecular Stratification of Multiple Sclerosis and Associated Neuro-autoimmune Di
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批准号:8734968
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项目类别:
-
资助金额:$24.65万
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财政年份:2013
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负责人:Robert C Axtell
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依托单位:
Molecular Stratification of Multiple Sclerosis and Associated Neuro-autoimmune Di
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批准号:8726564
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项目类别:
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资助金额:$24.9万
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财政年份:2013
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负责人:Robert C Axtell
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依托单位:
Molecular Stratification of Multiple Sclerosis and Associated Neuro-autoimmune Di
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批准号:8262668
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项目类别:
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资助金额:$8.93万
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财政年份:2011
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负责人:Robert C Axtell
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依托单位:
Molecular Stratification of Multiple Sclerosis and Associated Neuro-autoimmune Di
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批准号:8165160
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项目类别:
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资助金额:$8.96万
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财政年份:2011
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负责人:Robert C Axtell
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依托单位:
海外基金