NK Cell Interactions in Transplantation
NK Cell Interactions in Transplantation
批准号:
7191634
负责人:
Sheri M. Krams
金额:
$33.96万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1999
资助国家:
美国
项目状态:
已结题
起止时间:
1999-06-01 至 2010-02-28
关键词:
Activated LymphocyteActivated Natural Killer CellAddressAllograftingApoptosisApoptoticCD8B1 geneCell CommunicationCellsChimerismCytolysisDataEquilibriumFamily memberGoalsGraft RejectionGraft SurvivalGrantImmune responseImmune systemImmunosuppressive AgentsInterferonsLeadLigandsLiverMHC Class I GenesMediatingModelingMolecularNK Cell ActivationNatural Killer CellsOperative Surgical ProceduresOrgan TransplantationOutcomePathway interactionsPatternPersonal SatisfactionPlayProcessProductionProgress ReportsRattusReagentReperfusion InjuryResearch PersonnelRoleSignal TransductionSolidSourceStressStudy modelsSurfaceT-LymphocyteTestingTitleTransplantationVirusbasecell typechemokinecytokinecytotoxicityfunctional outcomesgraft functionkillingsliver allograftliver transplantationneoplastic cellnovelnovel strategiespreventprogramsreceptorresearch study
中文摘要
描述(由申请人提供):最近的证据表明,在实体器官移植中,先天性免疫系统在移植物排斥反应和诱导耐受中的重要性。然而,参与这些过程的先天免疫系统的特定细胞类型和分子尚未确定。我们已经开始在实体器官移植的背景下定义自然杀伤(NK)细胞的激活。我们已经证明,移植后早期NK细胞占肝脏浸润性细胞的大部分。这些NK细胞功能活跃,能产生大量的干扰素。此外,NK细胞的耗尽会导致干扰素水平降低。并延长移植物存活时间。基于这些数据,我们建议了一种模型,在该模型中,手术应激和缺血/再灌注损伤刺激同种异体肝移植,以诱导几种趋化因子的早期表达,这些趋化因子引导受体来源的NK细胞在移植后早期招募到同种异体移植物中。干扰素-?由NK细胞产生的淋巴细胞进一步诱导活化的淋巴细胞向移植物募集,从而增强效应器功能和移植物损伤。我们假设先天免疫系统,特别是NK细胞的激活,影响移植后的移植结果。这一假说将通过大鼠原位肝移植模型进行验证,以检验NK细胞在移植物排斥反应和移植物长期存活中的作用。在第一个具体目标中,我们将确定NK细胞在肝移植后移植结果中的作用。我们将:1)分析移植后NK细胞的作用;2)测定NK细胞耗竭对趋化因子和干扰素的影响。移植后的产生和细胞毒作用,3)分析在没有NK细胞的情况下混合嵌合体的建立,4)确定免疫抑制剂对NK细胞效应功能的影响。第二个特定目标的目标是确定特定NK细胞受体在移植结果中的功能意义。我们开发和组装的独特试剂将被用于在实体器官移植的背景下专门研究大鼠NK细胞受体的表达和功能意义。具体地说,我们将:1)确定移植后NK细胞激活受体的表达模式,2)确定通过NK细胞受体传递的信号是否诱导细胞因子的产生和细胞毒作用,3)检测阻断NK细胞受体在移植模型中的功能结果。我们的研究将明确NK细胞在同种异体移植排斥和接受中的功能意义,并将导致诱导同种异体肝移植耐受的新方法。
英文摘要
DESCRIPTION (provided by applicant): Recent evidence indicates the importance of the innate immune system in both graft rejection and the induction of tolerance in solid organ transplantation. However, the specific cell types and molecules of the innate immune system involved in these processes have not been determined. We have begun to define natural killer (NK) cell activation in the context of solid organ transplantation. We have shown that NK cells comprise the majority of liver infiltrating cells early post-transplantation. These NK cells are functionally active and producing substantial amounts of IFN-?. Furthermore, depletion of NK cells results in decreased levels of IFN-? and prolonged graft survival. Based on these data we suggest a model in which surgical stress and ischemia/reperfusion injury stimulate the liver allograft to induce the early expression of several chemokines that direct the recruitment of recipient-derived NK cells into the allograft early after transplantation. IFN-? produced by NK cells further induces the recruitment of activated lymphocytes to the graft thereby augmenting effector function and graft damage. We hypothesize that the innate immune system, specifically the activation of NK cells, influences graft outcome post transplantation. This hypothesis will be tested using a rat orthotopic liver transplant model to examine the role of NK cells during graft rejection and long term graft survival. In the first Specific Aim we will determine the role of NK cells in graft outcome following liver transplantation. We will: 1) analyze the role of NK cells post-transplant, 2) determine the effect of NK cell depletion on chemokine and IFN-? production and cytotoxicity post-transplant, 3) analyze the establishment of mixed chimerism in the absence of NK cells and 4) determine the effect of Immunosuppressive agents on NK cell effector function. The goal of the second specific aim is to determine the functional significance of specific NK cell receptors in graft outcome. Unique reagents we have developed and assembled, will be used, to specifically address the expression and functional significance of the rat NK cell receptors in the context of solid organ transplantation. Specifically we will: 1) determine the expression pattern of NK cell activation receptors after transplant, 2) determine if signaling through NK cell receptors induces cytokine production and cytotoxicity, and 3) examine the functional outcome of blocking NK cell receptors in a transplant model. Our studies will specifically define the functional significance of NK cells in both allograft rejection and acceptance and will lead to new approaches to induce tolerance to liver allografts.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Epstein Barr Virus Driven Mechanisms of Post Transplant Lymphoproliferative Disease
-
批准号:10755055
-
项目类别:
-
资助金额:$62.79万
-
财政年份:2023
-
负责人:Sheri M. Krams
-
依托单位:
Exosomes and the Immune Response in Allograft Outcomes in Pediatric Transplant Recipients
-
批准号:10612125
-
项目类别:
-
资助金额:$75.0万
-
财政年份:2022
-
负责人:Sheri M. Krams
-
依托单位:
Exosomes and the Immune Response in Allograft Outcomes in Pediatric Transplant Recipients
-
批准号:10339207
-
项目类别:
-
资助金额:$218.88万
-
财政年份:2021
-
负责人:Sheri M. Krams
-
依托单位:
Exosomes and the Immune Response in Allograft Outcomes in Pediatric Transplant Recipients
-
批准号:10188897
-
项目类别:
-
资助金额:$103.25万
-
财政年份:2020
-
负责人:Sheri M. Krams
-
依托单位:
Plasmacytoid Dendritic Cell microRNAS in Transplantation
-
批准号:9302655
-
项目类别:
-
资助金额:$20.04万
-
财政年份:2016
-
负责人:Sheri M. Krams
-
依托单位:
Functional Roles of NKp46 in Transplantation
-
批准号:8717580
-
项目类别:
-
资助金额:$19.69万
-
财政年份:2013
-
负责人:Sheri M. Krams
-
依托单位:
Functional Roles of NKp46 in Transplantation
-
批准号:8460369
-
项目类别:
-
资助金额:$22.19万
-
财政年份:2013
-
负责人:Sheri M. Krams
-
依托单位:
Tolerance Induction and Viral Infection in Liver Transplantation
-
批准号:8084888
-
项目类别:
-
资助金额:$40.12万
-
财政年份:2010
-
负责人:Sheri M. Krams
-
依托单位:
NK Cell Interactions in Transplantation
-
批准号:7872165
-
项目类别:
-
资助金额:$22.0万
-
财政年份:2009
-
负责人:Sheri M. Krams
-
依托单位:
IMMUNE-MEDIATED BILE DUCT INJURY IN BILIARY ATRESIA
-
批准号:6091826
-
项目类别:
-
资助金额:$7.82万
-
财政年份:2000
-
负责人:Sheri M. Krams
-
依托单位:
IMMUNE-MEDIATED BILE DUCT INJURY IN BILIARY ATRESIA
-
批准号:6381830
-
项目类别:
-
资助金额:$7.82万
-
财政年份:2000
-
负责人:Sheri M. Krams
-
依托单位:
APOPTOSIS IN TRANSPLANTATION
-
批准号:6632178
-
项目类别:
-
资助金额:$28.91万
-
财政年份:1999
-
负责人:Sheri M. Krams
-
依托单位:
NK Cell Interactions in Transplantation
-
批准号:7382580
-
项目类别:
-
资助金额:$33.39万
-
财政年份:1999
-
负责人:Sheri M. Krams
-
依托单位:
APOPTOSIS IN TRANSPLANTATION
-
批准号:6170880
-
项目类别:
-
资助金额:$26.45万
-
财政年份:1999
-
负责人:Sheri M. Krams
-
依托单位:
NK Cell Interactions in Transplantation
-
批准号:7071474
-
项目类别:
-
资助金额:$34.8万
-
财政年份:1999
-
负责人:Sheri M. Krams
-
依托单位:
NK Cell Interactions in Transplantation
-
批准号:7105908
-
项目类别:
-
资助金额:$23.27万
-
财政年份:1999
-
负责人:Sheri M. Krams
-
依托单位:
APOPTOSIS IN TRANSPLANTATION
-
批准号:6374008
-
项目类别:
-
资助金额:$27.25万
-
财政年份:1999
-
负责人:Sheri M. Krams
-
依托单位:
APOPTOSIS IN TRANSPLANTATION
-
批准号:6511149
-
项目类别:
-
资助金额:$28.06万
-
财政年份:1999
-
负责人:Sheri M. Krams
-
依托单位:
NK Cell Interactions in Transplantation
-
批准号:7574496
-
项目类别:
-
资助金额:$33.46万
-
财政年份:1999
-
负责人:Sheri M. Krams
-
依托单位:
SIXTH BASIC SCIENCE SYMPOSIUM OF TRANSPLANTATION
-
批准号:2875922
-
项目类别:
-
资助金额:$0.2万
-
财政年份:1999
-
负责人:Sheri M. Krams
-
依托单位: