Keystone Symposia Meetings on NK and NKT Cell Biology and Innate Immunity
Keystone Symposia Meetings on NK and NKT Cell Biology and Innate Immunity
批准号:
7407677
负责人:
ANDREW D ROBERTSON
金额:
$1.0万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-01-15 至 2008-12-31
关键词:
AreaAutoimmunityB-LymphocytesBiologyCellsCellular biologyCollaborationsColoradoDataDiagnosticDiseaseFamilyFosteringHost DefenseImmuneImmune responseInfectionInflammatoryLeadMediatingMolecularNatural ImmunityNatural Killer CellsNaturePathogenesisPlayProtein KinaseProteinsResearchResearch PersonnelRoleShapesSignal TransductionT-LymphocyteTimeToll-like receptorsTumor ImmunityWorkabstractingadapter proteinbasecell typedefense responsedrug developmentimmunopathologyinsightinterestmicrobialpathogenpreventreceptorresponsesymposiumtranscription factortumor
中文摘要
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英文摘要
ABSTRACT
This proposal is to request support for a pair of concurrent 2008 Keystone Symposia meetings entitled "NK and
NKT Cell Biology" (organized by Michael B. Brenner and Lewis L. Lanier), and "Innate Immunity: Signaling
Mechanisms" (organized by Luke A.J. O'Neill, J¿rg Tschopp and Shizuo Akira), which will be held in Keystone,
Colorado from February 24 - 29, 2008. NK cells and NKT cells play a central role in orchestrating and
amplifying the innate response - and in shaping the nature of the adaptive response of T cells and B cells.
The NK and NKT Cell Biology meeting will bring together, for the first time, researchers focusing on NK cells
and NKT cells. This should initiate discussions, foster collaborations and lead to a better understanding how
these cells use independent recognition mechanisms to achieve common effector functions and work
coordinately to mediate immune responses against tumors and pathogens, as well as influence autoimmunity.
With regard to the meeting on Innate Immunity: Signaling Mechanisms, the past 5 years has seen remarkable
progress in our understanding of the molecular basis for innate immunity. New families of receptors have been
discovered that sense microbial products, including Toll-like receptors (TLRs), NOD-like receptors (NLRs) and
RIG-I-like receptors. In addition, signaling mechanisms activated by these receptor families have been
described, with new adapter proteins, protein kinases and transcription factors being found. Breakthroughs in
our understanding of signaling mechanisms is a key aspect for this field, with much excitement and insight
being generated. This Keystone Symposia meeting will assemble the world's leading investigators in cell
signaling during innate immunity, to present recent data and discuss the importance of signaling in the more
general context of innate immunity. We can expect a compelling and informative meeting that will bring
together basic researchers in the area but also those more generally interested in leading edge research in
innate immunity. The pairing of these two Keystone Symposia meetings will stimulate productive interactions
between experts in the areas of NK/NKT biology and innate immunity.
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