NK Cell Interactions in Transplantation
NK Cell Interactions in Transplantation
批准号:
7872165
负责人:
Sheri M. Krams
金额:
$22.0万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-12 至 2011-08-31
关键词:
Activated LymphocyteActivated Natural Killer CellAddressAllograftingApoptosisApoptoticCD8B1 geneCell CommunicationCellsChimerismCytolysisDataEquilibriumFamily memberGoalsGraft RejectionGraft SurvivalGrantImmune responseImmune systemImmunosuppressive AgentsLeadLigandsLiverMHC Class I GenesMediatingModelingMolecularNK Cell ActivationNatural Killer CellsOperative Surgical ProceduresOrgan TransplantationOutcomePathway interactionsPatternPlayProcessProductionProgress ReportsRattusReagentReperfusion InjuryResearch PersonnelRoleSignal TransductionSolidSourceStressStudy modelsSurfaceT-LymphocyteTestingTransplantationVirusbasecell typechemokinecytokinecytotoxicityfunctional outcomesgraft functionkillingsliver allograftliver transplantationneoplastic cellnovelnovel strategiespreventprogramsreceptorresearch study
中文摘要
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英文摘要
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-y. Furthermore, depletion of NK cells results in decreased
levels of IFN-y 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-y 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-y 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 an will lead to new approaches to induce tolerance to liver
allografts.
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DOI:
10.1002/eji.200939779
发表时间:
2010-06
期刊:
EUROPEAN JOURNAL OF IMMUNOLOGY
影响因子:
5.4
作者:
[Zhuo, Ming, Fujiki, Masato, Wang, Mouer, Piard-Ruster, Karine, Wai, Lu-En, Wei, Liang, Martinez, Olivia M., Krams, Sheri M.]
通讯作者:
Krams, Sheri M.
DOI:
10.4049/jimmunol.1002597
发表时间:
2011-01-01
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
作者:
[Wai LE, Garcia JA, Martinez OM, Krams SM]
通讯作者:
Krams SM
DOI:
10.1111/j.1399-3046.2012.01653.x
发表时间:
2012-03
期刊:
Pediatric transplantation
影响因子:
1.3
作者:
[Pham B, Piard-Ruster K, Silva R, Gallo A, Esquivel CO, Martinez OM, Krams SM]
通讯作者:
Krams SM
Natural killer cells as modulators of alloimmune responses.
自然杀伤细胞作为同种免疫反应的调节剂。
DOI:
10.1097/mot.0000000000000590
发表时间:
2019
期刊:
Current opinion in organ transplantation
影响因子:
2.2
作者:
[Mbiribindi,Berenice, Harden,JamesT, Pena,JosselynK, Krams,SheriM]
通讯作者:
Krams,SheriM
Mutations to bid cleavage sites protect hepatocytes from apoptosis after ischemia/reperfusion injury.
bid裂解位点突变可保护肝细胞在缺血/再灌注损伤后免于凋亡。
DOI:
10.1097/01.tp.0000281555.18782.2b
发表时间:
2007
期刊:
Transplantation
影响因子:
6.2
作者:
[Riddle-Taylor,Erica, Nagasaki,Kazuhito, Lopez,Joseph, Esquivel,CarlosO, Martinez,OliviaM, Krams,SheriM]
通讯作者:
Krams,SheriM
共 7 条
Epstein Barr Virus Driven Mechanisms of Post Transplant Lymphoproliferative Disease
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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:
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:
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: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:
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:7191634
-
项目类别:
-
资助金额:$33.96万
-
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: