Antibody/Fusion Protein Core
Antibody/Fusion Protein Core
批准号:
7893570
负责人:
Mohamed Oukka
金额:
$14.73万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至
关键词:
ARHGEF5 geneAgonistAntibodiesAntigen-Presenting CellsAutoimmune DiseasesBindingBiological ProcessCell LineCell Surface ProteinsCell surfaceChimeric ProteinsClinical TrialsCollaborationsComplementary DNAConsultationsDataDiseaseFamilyFutureGalactose Binding LectinGene FamilyGenerationsGenesGoalsGrantHalf-LifeHamstersHandHospitalsHumanImmunityImmunizationImmunoglobulin GIn VitroIndividualInstitute of Medicine (U.S.)IsraelLaboratoriesLigandsMalignant NeoplasmsMedical centerModelingMonoclonal AntibodiesMusNeurologicPrincipal InvestigatorProductionProtein IsoformsProteinsQualifyingQuality ControlRattusReagentRecording of previous eventsResearchResearch PersonnelResearch Project GrantsRoleSpecificitySurfaceSystemT-LymphocyteTechniquesTestingTransplantationTransplantation ToleranceWomanWorkcostcytokinehuman diseaseimmunogenicityin vivoinnovationmeetingsnovel therapeuticspolyclonal antibodyprogramsreceptorreceptor bindingtool
中文摘要
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英文摘要
We have been successful in our effort to create and characterize a panel of monoclonal antibodies and Ig
related fusion proteins. Various different techniques, including cDNA immunization have been successfully
used in Dr. Kuchroo' laboratory to make monoclonal antibodies to soluble and cell surface proteins. We
have made antibodies to mouse, human, rat and hamster proteins. In addition, Dr. Zheng has successfully
generated dozens of Ig-fusion proteins. To understand biological functions of a newly identified protein, Ig
fusion proteins have been utilized for identifying in vitro and in vivo function of the molecules. In this effort
cytokines or cell surface proteins have been fused with the heavy chain of IgG, and we have recently
established a collaborative core between Xin Xiao Zheng, Vijay Kuchroo and Terry B. Strom to build a
antibody and fusion protein Core within the Transplant Research Center at Beth Israel Deaconess Medical
Center and Center for Neurologic Diseases, Brigham and Women's Hospital. Both Centers are located in
the Harvard Institutes of Medicine. The investigators meet regularly for planned meeting for impromptu
consultation. The investigators have a long history of working together and producing monoclonal
antibodies and fusion proteins to a number of cell surface targets. The recent collaboration has led to the
generation of monoclonal antibodies and Ig fusion proteins to TIM family of molecules, a family of newly
discovered immunoregulatory molecules expressed on the surface of T cells. The antibodies against
specific proteins can be generated that can act as an agonist and activate the receptor or an antagonist
and block the function of the molecule. Ig fusion proteins, on the other hand, have an advantage of
binding to the natural ligand and can be utilized as tools to identify and molecularly clone the ligand.
Furthermore, Ig fusion proteins can act as blocking agents and interfere with the binding of receptor:ligand
interaction and therefore help in the understanding the in vivo function of the molecule. Ig proteins also
have long half-lives and minimal immunogenicity, therefore can be used successfully in vivo for
understanding the function of the newly identified molecule. The antibodies and Ig fusion proteins are
unique reagents and have been proven to be a powerful tools to facilitate innovative research in many
fields and some have proven to be potent immunomodulatory reagents to treat human autoimmune
diseases, cancer and induce transplantation tolerance.
The goals of antibody and fusion protein Core will be to provide a platform for developing monoclonal and
polyclonal antibodies and novel therapeutic Ig.fusion proteins for newly discovered molecules or genes for
PPG. Our role will be to provide antibodies and fusion proteins for newly identified proteins. While the
proteins produced by the core will not be manufactured in a GMP facility, the cell lines used for production
will meet FDA standards. Thus it will be possible to easily progress to a clinical trial in the future.
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Effector Function of Regulatory T Cells in EAE
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批准号:9470744
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项目类别:
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资助金额:$28.25万
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财政年份:2018
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负责人:Mohamed Oukka
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依托单位:
Role of Dock8 in EAE
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批准号:9125526
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资助金额:$28.94万
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财政年份:2016
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Role of Dock8 in EAE
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批准号:9324123
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资助金额:$24.11万
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财政年份:2016
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负责人:Mohamed Oukka
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依托单位:
Role of S1P1 in the function of Regulatory T cells in Autoimmune Encephalomyeliti
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批准号:8889765
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项目类别:
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资助金额:$48.5万
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财政年份:2014
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负责人:Mohamed Oukka
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依托单位:
Role of interlukin 23 and innate lymphoid cells in protective immunity
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批准号:8360975
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项目类别:
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资助金额:$29.1万
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财政年份:2012
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负责人:Mohamed Oukka
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依托单位:
Role of interlukin 23 and innate lymphoid cells in protective immunity
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批准号:8499252
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项目类别:
-
资助金额:$22.8万
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财政年份:2012
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负责人:Mohamed Oukka
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依托单位:
Trafficking and the role of myelin specific Regulatory T cells in EAE
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批准号:8105664
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项目类别:
-
资助金额:$29.25万
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财政年份:2010
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负责人:Mohamed Oukka
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依托单位:
Trafficking and the role of myelin specific Regulatory T cells in EAE
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批准号:7778249
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项目类别:
-
资助金额:$42.61万
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财政年份:2007
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负责人:Mohamed Oukka
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依托单位:
Trafficking and the role of myelin specific Regulatory T cells in EAE
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批准号:8026713
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项目类别:
-
资助金额:$5.23万
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财政年份:2007
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负责人:Mohamed Oukka
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依托单位:
Trafficking and the role of myelin specific Regulatory T cells in EAE
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批准号:7393123
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项目类别:
-
资助金额:$35.5万
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财政年份:2007
-
负责人:Mohamed Oukka
-
依托单位:
Trafficking and the role of myelin specific Regulatory T cells in EAE
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批准号:8039245
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项目类别:
-
资助金额:$42.18万
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财政年份:2007
-
负责人:Mohamed Oukka
-
依托单位:
Trafficking and the role of myelin specific Regulatory T cells in EAE
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批准号:7579016
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项目类别:
-
资助金额:$30.27万
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财政年份:2007
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负责人:Mohamed Oukka
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依托单位:
Trafficking and the role of myelin specific Regulatory T cells in EAE
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批准号:7242152
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项目类别:
-
资助金额:$36.19万
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财政年份:2007
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负责人:Mohamed Oukka
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依托单位:
Antibody/Fusion Protein Core
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批准号:8113324
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项目类别:
-
资助金额:$14.99万
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财政年份:--
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负责人:Mohamed Oukka
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依托单位:
Antibody/Fusion Protein Core
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批准号:8298450
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项目类别:
-
资助金额:$26.04万
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财政年份:--
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负责人:Mohamed Oukka
-
依托单位:
Antibody/Fusion Protein Core
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批准号:8378187
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项目类别:
-
资助金额:$21.35万
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财政年份:--
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负责人:Mohamed Oukka
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依托单位:
国内基金
海外基金
Agonist-GPR119-Gs复合物的结构生物学研究
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批准号:32000851
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项目类别:青年科学基金项目
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资助金额:24.0万元
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批准年份:2020
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负责人:乔安娜
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依托单位: