Antibodies and complement in ischemia reperfusion injury and regeneration
Antibodies and complement in ischemia reperfusion injury and regeneration
批准号:
9090080
负责人:
Stephen Tomlinson
金额:
$45.42万
依托单位国家:
美国
项目类别:
财政年份:
2015
资助国家:
美国
项目状态:
已结题
起止时间:
2015-07-01 至 2019-06-30
关键词:
AddressAnnexin A4AntibodiesBindingBlood VesselsBurn injuryCellsClinicalComplementComplement 1qComplement 3d ReceptorsComplement ActivationComplement InactivatorsComplement Membrane Attack ComplexDataDepositionEndothelial CellsEpitopesEquilibriumEventExcisionGoalsHealthHemorrhagic ShockHepaticHepatocyteHomeostasisHumanHypoxiaImmuneImmunoglobulin MIn VitroInflammationInflammatoryInjuryInvestigationIschemiaKupffer CellsLinkLipidsLiverLiver RegenerationMass Spectrum AnalysisMetabolic stressModelingMolecularMolecular ProfilingMusMyocardial InfarctionNatural regenerationNecrosisNeutrophil InfiltrationNormal CellOperative Surgical ProceduresOpsoninOrgan TransplantationPartial HepatectomyPathogenicityPathway interactionsPatternPattern recognition receptorPhospholipidsPlayProteinsProtocols documentationPublishingRag1 MouseReactionReagentRecoveryReperfusion InjuryRoleSepsisSerumSpecificitySterilityStressStrokeStudy modelsSystemTechniquesTherapeuticTimeTissuesTransplantationactivation productbaseclinically relevantimmunogenicimproved outcomein vivo Modelinhibitor/antagonistinjuredliver injuryliver ischemiamacrophagemouse modelnew therapeutic targetnovelprotective effectreconstitutionregenerativescreeningtargeted treatmenttherapeutic targettissue repairtool
中文摘要
英文摘要
DESCRIPTION (provided by applicant): Natural self-reactive IgM antibodies represent a class of innate pattern recognition receptors that recognize danger associated molecular patterns (DAMPS) as neoepitopes expressed on stressed or dying cells. Recognition of these neoepitopes by IgM activates complement, initiating an inflammatory reaction, which can have injurious as well as protective effects. The overall goals of this project are to better characterie the innate immunogenic alterations that occur following ischemia and stress, to fully characterize the neoepitopes that serve as DAMPs, and to understand the complement activation event and complement effector mechanisms involved in the balance between sterile inflammation and injury on the one hand, and tissue repair/regeneration on the other. Complement inhibitors will be used in mouse models as therapeutically relevant investigative tools, and the focus of the studies will be on hepatic ischemia reperfusion injury and regeneration.
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