Analysis of Differential Resistance Emergence Risk for Differential Treatment App
Analysis of Differential Resistance Emergence Risk for Differential Treatment App
批准号:
7685982
负责人:
RYAN M ZURAKOWSKI
金额:
$20.48万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-06-05 至 2011-05-31
关键词:
AdherenceAlgorithmsAntiviral AgentsAntiviral TherapyCD4 Positive T LymphocytesCell CountCessation of lifeClinicalClinical TrialsDataDevelopmentDisease MarkerEvolutionExperimental DesignsFailureFutureGenerationsGeneticGoalsHIVImmunologic Deficiency SyndromesIncidenceInfectionInterruptionKnowledgeLaboratoriesLeadLeftLife Cycle StagesLife ExpectancyMapsMediatingMethodsModelingMulti-Drug ResistanceMutationOpportunistic InfectionsPatientsPatternPharmaceutical PreparationsPopulationPredispositionPreparationPrincipal InvestigatorProbabilityQuality of lifeRNA-Directed DNA PolymeraseRecommendationRecording of previous eventsResearchResearch Project GrantsResistanceResistance developmentRetroviridaeRiskSamplingScheduleStatistical ModelsTarget PopulationsTechniquesTimeTreatment FailureTreatment ProtocolsVariantViralViral Load resultVirusWorkbasedrug resistant virusimprovedmathematical modelpredictive modelingprogramspublic health relevanceresearch studyresistant strainsuccessvirus genetics
中文摘要
描述(由申请方提供):本项目将开发基于模型的HIV治疗转换方法,通过同时考虑病毒和前病毒基因组成以及总病毒载量对该风险的贡献,最大限度地降低后续治疗失败的风险。使用以前失败的抗病毒治疗方案的成分,患者的病毒载量将为新的抗病毒治疗方案进行“预处理”,以最大限度地提高其成功的可能性。这种方法在几个重要方面不同于以前的方法。它关注的是尚未出现多重耐药病毒的患者的治疗转换,对他们来说,潜在的成功抗病毒方案仍然存在。它不仅将已知的抗病毒药物之间的交叉耐药性发生率纳入其风险计算中,而且还将基于患者的抗病毒药物使用史的显性耐药菌株之间的遗传距离的知识纳入其中。这些治疗方法将基于艾滋病毒准种动力学的数学模型和不同治疗应用时间表期间各种病毒株之间的竞争,以及耐药性出现的数学模型。这些模型将用于开发实验室和临床实验,作为未来实施这些技术的工作。基于模型的算法治疗转换方案应通过降低引入之前存在的耐药病毒的风险,显著降低后续抗病毒治疗失败的风险。公共卫生相关性:如果成功,这项研究将提供一种方法,以减少艾滋病毒治疗失败的发生率,由于耐药病毒。这有可能延长成千上万艾滋病毒感染者的预期寿命,并改善他们的生活质量。该方法的应用还可以降低人群中多重耐药病毒的总体发生率。
英文摘要
DESCRIPTION (provided by applicant): This project will develop model-based approaches to therapy switching for HIV which minimize the risk of subsequent treatment failures by simultaneously considering the contributions of the viral and proviral genetic makeup and the total viral load to this risk. Using components of previously failed antiviral regimens, the patient's viral load will be "pre-conditioned" for the new antiviral regimen, to maximize its possibility of success. This approach differs from the previous approaches in several important ways. It focuses on therapy switches in patients who have not yet developed multi-drug resistant virus, for whom potentially successful antiviral regimens still exist. It incorporates into its calculation of risk not only the known incidences of cross-resistance between antiviral drugs, but also the knowledge of genetic distance between dominant resistant strains, based on the patient's history of antiviral use. These approaches to treatment will be based on mathematical models of HIV quasispecies dynamics and the competition between various viral strains during different treatment application schedules, as well as mathematical models of resistance emergence. These models will be used to develop laboratory and clinical experiments as future work to implement these techniques. The model- based algorithmic therapy-switching schedules should significantly reduce the risk of failure of subsequent antiviral therapy by reducing the risk of resistant virus pre-existing its introduction. PUBLIC HEALTH RELEVANCE: If successful, this research will provide a method to reduce the incidence of HIV treatment failure due to resistant virus. This has the potential to extend the life expectancy of thousands of people infected with the HIV virus, and to improve their quality of life. Application of this method may also reduce the overall incidence of multi-drug resistant virus in the population.
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专著(0)
科研奖励(0)
会议论文
HIV 2-LTR Dynamics and Cryptic Viremia
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批准号:8732302
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项目类别:
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资助金额:$21.48万
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财政年份:2014
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负责人:RYAN M ZURAKOWSKI
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依托单位:
Analysis of Differential Resistance Emergence Risk for Differential Treatment App
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批准号:7860447
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项目类别:
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资助金额:$19.13万
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财政年份:2009
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负责人:RYAN M ZURAKOWSKI
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依托单位:
海外基金