Ubiquitous pollutant acrolein inhibits IFN?? antiviral signaling: relevance to HC
无处不在的污染物丙烯醛抑制干扰素??
基本信息
- 批准号:8009501
- 负责人:
- 金额:$ 13.11万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2010
- 资助国家:美国
- 起止时间:2010-01-01 至 2014-12-31
- 项目状态:已结题
- 来源:
- 关键词:AcroleinAcrylatesAir PollutantsAlcohol abuseAldehydesAlzheimer&aposs DiseaseAmino AcidsAntiviral AgentsAtherosclerosisAutomobile ExhaustBindingBiocideBiological MarkersBiological ModelsBiologyBiopsy SpecimenCell LineCessation of lifeChemical WeaponsChronicChronic DiseaseChronic Hepatitis CCirrhosisClinicalClinical ResearchCysteineDataDevelopmentDiabetes MellitusDiseaseDoseDouble-Stranded RNAEnvironmentEnvironmental ExposureEnvironmental PollutantsExposure toFDA approvedFailureFamilyFatty acid glycerol estersFoodFree RadicalsFunctional disorderFutureGene ExpressionGenesGenotypeHepatitis CHepatitis C virusHepatocyteHistidineHumanHydroxyl RadicalImidazoleIn VitroIndividualIndustrial WasteInflammationInterferonsKidney FailureLigand BindingLigaseLipid PeroxidationLiteratureLiverLiver diseasesLysineMediatingMedicineMessenger RNAMetabolismMethionineModelingModificationMolecularMusNon-Insulin-Dependent Diabetes MellitusNucleic AcidsObesityOrganic ChemicalsOutcomeOxidative StressPTPN11 genePathway interactionsPatientsPegylated Interferon AlfaPhospholipidsPhosphorylationPlasticsPlayPolyaminesPolymersPrimary carcinoma of the liver cellsProtein Phosphatase 2A Regulatory Subunit PR53Protein Tyrosine KinaseProtein phosphataseProteinsPublicationsPublishingRattusRegimenRepliconReportingResearchResearch PersonnelResistanceResponse ElementsRibavirinRoleSTAT proteinSTAT1 geneSTAT2 geneSerumSideSignal TransductionSmokeSmokerSmokingSourceSpecimenStagingSystemTYK2TestingTherapeuticTissuesTranscriptional ActivationTreatment outcomeUnited StatesUnited States Environmental Protection AgencyUrineVaccinesViralWaterWater PollutantsWood materialadductamino groupanti-hepatitis Cbasecigarette smokingcigarette smokingcofactorcookingeIF-2 Kinaseefficacy testingglobal healthimprovedin vivoinsightliver biopsymouse modelnon-smokernovel therapeutic interventionoligoadenylatepollutantprotein activationpublic health relevancereceptorreceptor internalizationresponsestandard of caretherapy outcome
项目摘要
DESCRIPTION (provided by applicant): Chronic Hepatitis C virus (HCV) infection remains a global health concern with nearly 200 million carriers worldwide. It can be a precursor to cirrhosis, hepatocellular carcinoma and end-stage liver disease. In the absence of a vaccine, the current FDA approved standard of care for chronic hepatitis C is a combination of pegylated interferon-alpha (IFN1) and ribavirin. Unfortunately, this regimen is only effective in about 50% of patients, emphasizing the need for studies defining the molecular mechanisms underlying resistance to IFN1. Clinical studies have identified several potential cofactors that may contribute to the failure of anti-HCV therapy, including obesity, diabetes, alcohol abuse, oxidative stress, cigarette smoking and environmental pollutants. Acrolein is a ubiquitous, highly reactive environmental and industrial pollutant, and is designated by the U.S. Environmental Protection Agency (EPA) as a high priority air and water pollutant. Notably, acrolein is also formed endogenously as a byproduct of lipid peroxidation (LPO) and is, itself, known to cause oxidative stress. Moreover, acrolein is a major component of cigarette smoke and recent studies suggest that smokers with chronic hepatitis C have a lower response rate to IFN1 compared to non-smokers. We have convincing preliminary data showing that non-toxic concentrations of acrolein significantly down-regulate IFN1 signaling and antiviral gene expression in vitro (cultured human hepatic cells) and in vivo (mice). Published literature and our own compelling data strongly support our hypothesis that acrolein adversely influences IFN1 therapy outcomes by inhibiting or disrupting IFN1 mediated signaling and antiviral gene expression in hepatocytes, and that high acrolein exposure (environmental and/or endogenous) will correlate with poor IFN1 response in HCV infected individuals. Our hypotheses will be tested by examining the effects of acrolein on early IFN1-mediated signaling (including components of the Jak/STAT pathway) and antiviral gene expression using well established in vitro and in vivo experimental systems, as well as an HCV replicon that directly reports on HCV viral replication. Additionally, the investigators will establish a clinical/translational aspect of our hypothesis by conducting a retrospective analysis using banked serum, urine and/or liver biopsy samples from healthy, uninfected individuals and HCV-infected patients (responders and non-responders). This analysis will explore a possible correlation between acrolein exposure and poor IFN1 response (lack of sustained virologic response, SVR). The investigators expect their studies will elucidate critical mechanisms underlying resistance to IFN1 treatment and will identify potential targets for novel therapeutic intervention.
Public Health Relevance: Acrolein is one of the major reactive aldehydes ubiquitously present in foods, water and in the environment. It is a major constituent of cigarette smoke. Recent data suggest that HCV- infected smokers have worse IFN1 therapeutic outcomes compared with non-smokers. Acrolein is also generated endogenously due to cellular metabolism, and this may constitute a significant source of intracellular acrolein in situations of oxidative stress and inflammation. Elevated acrolein adducts have been detected in several disease conditions that are also known to be associated with failure of IFN therapy. Hence, based on available literature and the investigators' own compelling preliminary results, they have opted to use acrolein as the model compound for this study. The aim of the study is to determine the contribution of acrolein to the mechanisms of IFN1 resistance. The investigators have preliminary evidence to demonstrate that acrolein, at nontoxic concentrations, significantly down-regulates IFN1 signaling and antiviral/anti-HCV gene expression.
描述(申请人提供):慢性丙型肝炎病毒(丙型肝炎病毒)感染仍然是一个全球关注的健康问题,全世界有近2亿携带者。它可能是肝硬变、肝细胞癌和终末期肝病的前兆。在缺乏疫苗的情况下,目前FDA批准的慢性丙型肝炎的治疗标准是聚乙二醇化干扰素-α(IFN1)和利巴韦林的组合。不幸的是,这种方案只对大约50%的患者有效,强调需要研究确定对IFN1耐药的分子机制。临床研究已经确定了几个可能导致抗丙型肝炎病毒治疗失败的潜在辅助因素,包括肥胖、糖尿病、酗酒、氧化应激、吸烟和环境污染。丙烯醛是一种普遍存在的、高活性的环境和工业污染物,被美国环境保护局(EPA)指定为高度优先的空气和水污染物。值得注意的是,丙烯醛也是作为脂质过氧化(LPO)的副产物在体内形成的,本身就已知会导致氧化应激。此外,丙烯醛是香烟烟雾的主要成分,最近的研究表明,与不吸烟的人相比,患有慢性丙型肝炎的吸烟者对IFN1的应答率较低。我们有令人信服的初步数据表明,无毒浓度的丙烯醛在体外(培养的人肝细胞)和体内(小鼠)显著下调IFN1信号和抗病毒基因的表达。已发表的文献和我们自己令人信服的数据有力地支持了我们的假设,即丙烯醛通过抑制或干扰IFN1介导的信号和抗病毒基因在肝细胞中的表达而对IFN1治疗结果产生不利影响,并且高水平的丙烯醛暴露(环境和/或内源性)将与丙型肝炎病毒感染者较差的IFN1反应相关。我们的假设将通过使用成熟的体外和体内实验系统以及直接报告丙型肝炎病毒复制的丙型肝炎病毒复制子来检验丙烯醛对早期IFN1介导的信号传递(包括JAK/STAT途径的组件)和抗病毒基因表达的影响。此外,研究人员将通过使用来自健康、未感染的个人和感染丙型肝炎病毒的患者(应答者和无应答者)的库存血清、尿液和/或肝活检样本进行回顾分析,建立我们假设的临床/翻译方面。这项分析将探索丙烯醛暴露与IFN1反应差(缺乏持续病毒学反应,SVR)之间的可能相关性。研究人员预计,他们的研究将阐明对IFN1治疗产生耐药性的关键机制,并将确定新的治疗干预的潜在靶点。
与公共健康相关:丙烯醛是一种主要的反应性醛,广泛存在于食品、水和环境中。它是香烟烟雾的主要成分。最近的数据表明,与不吸烟的人相比,感染丙型肝炎病毒的吸烟者的IFN1治疗结果更差。丙烯醛也是由于细胞代谢而内源性产生的,这可能是氧化应激和炎症情况下细胞内丙烯醛的一个重要来源。已在几种已知与干扰素治疗失败相关的疾病中检测到丙烯醛加合物升高。因此,根据现有文献和研究人员自己令人信服的初步结果,他们选择使用丙烯醛作为本研究的模型化合物。这项研究的目的是确定丙烯醛在IFN1耐药机制中的作用。研究人员有初步证据表明,在无毒浓度下,丙烯醛显著下调IFN1信号和抗病毒/抗丙型肝炎病毒基因的表达。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Swati Joshi-Barve其他文献
Swati Joshi-Barve的其他文献
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{{ truncateString('Swati Joshi-Barve', 18)}}的其他基金
Lipid metabolites can both potentiate and treat alcoholic hepatitis
脂质代谢物可以增强和治疗酒精性肝炎
- 批准号:
9791137 - 财政年份:2018
- 资助金额:
$ 13.11万 - 项目类别:
Lipid metabolites can both potentiate and treat alcoholic hepatitis
脂质代谢物可以增强和治疗酒精性肝炎
- 批准号:
10202388 - 财政年份:2018
- 资助金额:
$ 13.11万 - 项目类别:
Lipid metabolites can both potentiate and treat alcoholic hepatitis
脂质代谢物可以增强和治疗酒精性肝炎
- 批准号:
10441376 - 财政年份:2018
- 资助金额:
$ 13.11万 - 项目类别:
Ubiquitous pollutant acrolein inhibits IFN?? antiviral signaling: relevance to HC
无处不在的污染物丙烯醛抑制干扰素??
- 批准号:
8212455 - 财政年份:2010
- 资助金额:
$ 13.11万 - 项目类别:
Ubiquitous pollutant acrolein inhibits IFN?? antiviral signaling: relevance to HC
无处不在的污染物丙烯醛抑制干扰素??
- 批准号:
8411149 - 财政年份:2010
- 资助金额:
$ 13.11万 - 项目类别:
Ubiquitous pollutant acrolein inhibits IFN?? antiviral signaling: relevance to HC
无处不在的污染物丙烯醛抑制干扰素??
- 批准号:
8599456 - 财政年份:2010
- 资助金额:
$ 13.11万 - 项目类别:
Ubiquitous pollutant acrolein inhibits IFN?? antiviral signaling: relevance to HC
无处不在的污染物丙烯醛抑制干扰素??
- 批准号:
7788500 - 财政年份:2010
- 资助金额:
$ 13.11万 - 项目类别:
Role of acrolein in hepatic ER stress adn injury in alcoholic liver disease
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10116878 - 财政年份:
- 资助金额:
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