CCR7 Chemotaxis Regulates Memory T Cell Localization
CCR7 Chemotaxis Regulates Memory T Cell Localization
批准号:
10341145
负责人:
CHARLOTTE M VINES
金额:
$37.75万
依托单位国家:
美国
项目类别:
财政年份:
2015
资助国家:
美国
项目状态:
已结题
起止时间:
2015-07-01 至 2024-01-31
关键词:
Adoptive TransferAntibodiesAntibody FormationAntibody titer measurementAntibody-Producing CellsAntigensAutoimmune DiseasesB-Cell ActivationB-LymphocytesBiological AssayBone MarrowCC chemokine receptor 7CD4 Positive T LymphocytesCXC ChemokinesCXCL12 geneCell CompartmentationCell Surface ProteinsCell physiologyCellsChemotaxisDataDendritic CellsEventExposure toGoalsHomingHumanImmuneImmune responseImmune systemImmunityImmunoglobulin Class SwitchingImmunologic MemoryImmunosuppressionIn VitroIndividualKnockout MiceKnowledgeLifeLigandsLinkMajor Histocompatibility ComplexMeasuresMemoryMemory B-LymphocyteMigration AssayMolecularMusPathogenicityPathway interactionsPatternPattern recognition receptorPeptidesPlasmaPlayPopulationProteomicsRegulationRegulatory T-LymphocyteRoleSignal TransductionSiteSpleenT memory cellT-Cell ProliferationT-LymphocyteTissuesUp-RegulationVaccinesWorkadaptive immune responseantagonistbeta-Chemokineschemokinechemokine receptorconditional knockouteffector T cellexposed human populationfallsgamma-Chemokinesimprovedin vitro Assayin vivolymph nodesmigrationnovelpathogenpreventreceptorresponsetargeted treatmenttherapeutic targettraffickingvaccine efficacy
中文摘要
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英文摘要
ABSTRACT When humans are exposed to a substance that causes an immune response, to protect the itself,
the body generates antibodies. There is very little understood about the role of chemokines in regulating the
extent of the immune response, as measured by antibody titers and types of antibodies that are made. We
have found that C-C chemokine receptor 7 regulates the antibody titers by controlling the localization of
different populations of immune cells to the bone marrow. In this proposal our goal is to better understand the
molecular mechanisms that are employed by immune T cells to respond to C-C chemokine receptor 7
activation that regulate the targeting of T cells to the bone marrow where they regulate the isotype switching
and antibody production by immune cells. Our study is important since these antibodies protect the host when
he or she is exposed to the same substance during a secondary immune response. We hypothesize that
CCR7 regulates the migration of memory T, and regulatory T cells to the bone marrow to limit the activation of
B cells during an adaptive immune response. With the knowledge we gain we will determine if redirection of
the T cells can be applied to inhibit excessive immune responses observed during autoimmune diseases.
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