Novel treatment for respiratory distress due to SARS-CoV2 infection
Novel treatment for respiratory distress due to SARS-CoV2 infection
批准号:
10284733
负责人:
Cynthia Ann Derdeyn
金额:
$23.46万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
已结题
起止时间:
2021-06-11 至 2023-05-31
关键词:
2019-nCoVACE2AblationAcute Renal Failure with Renal Papillary NecrosisAdult Respiratory Distress SyndromeAffectAnimal ModelAnimalsAnticoagulationAntineoplastic AgentsArteriesAttenuatedBindingBiological MarkersBloodBlood capillariesBlood coagulationCOVID-19COVID-19 patientCOVID-19 treatmentCOVID-19/ARDSCell Cycle RegulationCell NucleusCell membraneCellsClinicClinicalClinical TreatmentClinical TrialsCoagulation ProcessCytoskeletal ModelingDNA RepairDataDepressed moodDiseaseDown-RegulationDrug TargetingEdemaEndothelial CellsEndotheliumExhibitsExtracellular MatrixExtravasationFibrin fragment DFibrin split productsFocal AdhesionsFunctional disorderGelatinase AGeneticHeart failureHemorrhageImpairmentIn VitroIndividualInfiltrationInflammationInflammatoryInflammatory ResponseInjectionsInvestigationIschemiaIschemic StrokeLaboratoriesLeukocytesLipopolysaccharidesLiquid substanceLoxP-flanked alleleLungMaintenanceMalignant NeoplasmsMatrix MetalloproteinasesMetabolicMiddle Cerebral Artery OcclusionMitochondriaMultiple Organ FailureMusNADPH OxidaseOrgan failureOutcomePathologyPathway interactionsPatientsPermeabilityPharmacologyPolymeraseProductionProteinsPseudomonas aeruginosaReactive Oxygen SpeciesRespiratory distressSARS-CoV-2 infectionStrokeStructure of parenchyma of lungTNF geneTNFSF5 geneTailTestingThrombosisThrombusTissuesToxic effectTranslatingblood-brain barrier disruptioncytokinecytokine release syndromeimprovedin vivolung injurymonocytemouse modelneutrophilnovelpreservationpreventreceptorrecruitresponseresponse to injurysevere COVID-19therapeutic target
中文摘要
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英文摘要
SUMMARY
Clinical sequelae of COVID-19 patients include not only acute respiratory distress syndrome (ARDS), but also
often acute kidney injury and heart failure. These pathologies share endothelial activation as a common
underlying early response to injury, and endothelial cells express high levels of angiotensin converting enzyme
2 (ACE2), a functional receptor for SARS-CoV-2. Activated endothelium not only attracts and promotes
leukocyte infiltration into tissues and contributes to the cytokine storm resulting in capillary leakage and edema,
but is also prothrombotic. Together, these mechanisms result in tissue inflammation and ischemia, leading to
organ failure. Our laboratory discovered that polymerase delta interacting protein 2 (Poldip2) is a novel and
important regulator of inflammation, endothelial permeability and potentially coagulation in mice. Mice
heterozygous for Poldip2 are largely protected from lipopolysaccharide (LPS)- or P. aeruginosa-induced ARDS.
Here, we hypothesize that Poldip2 may be a novel target for treatment of SARS-CoV-2-infected individuals, as
downregulation of Poldip2 not only reduces ARDS complications such as edema and the cytokine storm, but
also potentially may inhibit thrombosis. To test this hypothesis, we propose to treat SARS-CoV-2-infected mice
with an anti-cancer agent undergoing clinical trials that we have recently shown to reduce Poldip2 levels and
restore endothelial barrier function. In the first Aim, we will use this agent to downregulate Poldip2 and test its
ability to preserve endothelial barrier function and reduce inflammation in response to SARS-CoV-2 infection in
mice. The second aim will focus on determining the effect of the anticancer agent and genetic ablation of Poldip2
on basal coagulation and that induced by SARS-CoV-2 infection. We anticipate that pharmacological
downregulation of Poldip2 will represent a promising new treatment for COVID-19 patients that can be rapidly
translated to the clinic.
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会议论文
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