Targeting Covid-19 with a Therapeutic Interfering Particle
Targeting Covid-19 with a Therapeutic Interfering Particle
批准号:
10256845
负责人:
Raul Andino
金额:
$30.0万
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:
2021-04-05 至 2023-03-31
关键词:
2019-nCoVA549ACE2AcuteAlpha ParticlesAnimal ExperimentsAnimal ModelAntiviral AgentsBody WeightBrunhilde VirusCOVID-19COVID-19 pandemicCell Culture TechniquesCellsClinicalClinical MarkersCoronavirusCoxsackie VirusesDataDevelopmentDiseaseDrug or chemical Tissue DistributionEnterovirusEpithelial CellsFundingFutureGoalsImmune responseInfectionInfluenza A virusInnate Immune ResponseK-18 conjugateLungLung diseasesMeasuresMessenger RNAMonitorMusOrganoidsProcessProductionPublic HealthRNARhinovirusSafetyStructure of respiratory epitheliumTherapeuticToxic effectTransgenic MiceViralVirusWorkbaseefficacy evaluationefficacy testingexperimental studylipid nanoparticlemouse modelnovel strategiesnovel therapeuticsparticlepreventprogramsprophylacticrespiratoryrespiratory virustreatment response
中文摘要
点击翻译按钮获取中文摘要
英文摘要
SUMMARY
The Covid-19 pandemic caused by Severe Acute Respiratory Coronavirus 2 (SARS-CoV-2) is currently
the most important public health crisis in the world. Given the unprecedented scope of this disease, it is critical
to explore novel strategies to mitigate this crisis. Aleph Therapeutics and UCSF have jointly developed eTIP1,
a Therapeutic Interfering Particle. eTIP1 was developed under a DARPA-funded program and shows potent
broad-spectrum activity across enteroviruses (Poliovirus Type 1 and 3, EVA71, and Coxsackievirus B3) as well
as respiratory viruses EV-D68/HRV-87, Rhinovirus A16 and A1B, and Influenza A. Recently we have shown
that eTIP1 significantly inhibits replication of SARS-CoV-2 both in cell culture and in K18-ACE2 mice. Given
these results, it is critical to thoroughly evaluate eTIP1 as a potential agent against SARS-CoV-2. This work
could be the starting point for a potential therapy or prophylactic agent against SARS-CoV-2. This would also
represent a significant breakthrough for the development of a broad-spectrum antiviral agent that could
potentially target current and future viral threats.
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Mapping spatiotemporal dynamics during enterovirus infection across cells and tissues
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Role of Protein Homeostasis in Enterovirus Population Diversity, Evolution and Pa
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依托单位:
Protein homeostasis mechanisms underlying enterovirus replication and evolution
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RNAi as an Intercellular Antiviral Defense Mechanism
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RNAi as an Intercellular Antiviral Defense Mechanism
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