Title: Role of Heparan sulfate in B-cell responses
Title: Role of Heparan sulfate in B-cell responses
批准号:
8501350
负责人:
LAURENT COSCOY
金额:
$16.5万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-07-01 至 2014-12-30
关键词:
AdhesionsAffectAffinityAntibodiesAntibody FormationAntigensAntiviral ResponseAutoimmunityB-LymphocytesBindingCell AdhesionCell physiologyCell surfaceCellsComplexDataDevelopmentEnsureExcisionExtracellular MatrixGrowth FactorHen Egg LysozymeHeparitin SulfateHerpesviridae InfectionsImmune responseImmune systemInfectionInfluenzaInterferonsLigandsModelingModificationMusPlayPoly CReportingRoleSeriesSignal TransductionSurfaceT-LymphocyteTestingUp-RegulationVaccinesVirusVirus DiseasesWild Type MouseWorkantigen bindingcell motilitychemokinecytokineextracellulargammaherpesvirusin vivopathogenpreventpublic health relevancereceptorresearch studyresponsesugaruptakevaccine developmentvaccinology
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Heparan sulfate (HS) influences many cellular processes including adhesion, motility, ligand-receptor interaction, and proliferation. We have recently observed that the expression of HS was tightly regulated on B-cells: whereas naive B-cells do not express heparan sulfate, all B-cells isolated from mice infected with viruses, or mice
injected with poly I:C, express heparan sulfate. Accordingly, B-cells treated ex-vivo with IFN-I alone express high level of heparan sulfate. Our preliminary data indicates that HS expression on B-cells regulates their responsiveness to cytokines as well as their motility in vivo. Here we propose experiments aimed at validating the importance of HS for mounting of an efficient antiviral response. This work might help in the understanding of B-cell responses and has strong implication for vaccine development and autoimmunity.
期刊论文(1)
专著(0)
科研奖励(0)
会议论文
DOI:
10.4049/jimmunol.1003495
发表时间:
2011-12-01
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
作者:
[Jarousse N, Trujillo DL, Wilcox-Adelman S, Coscoy L]
通讯作者:
Coscoy L
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海外基金