Efficacy of antiretroviral inhibitors in HIV cell-to-cell transmission
Efficacy of antiretroviral inhibitors in HIV cell-to-cell transmission
批准号:
8599743
负责人:
WALTHER H MOTHES
金额:
$8.33万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-01-01 至 2015-04-30
关键词:
Acquired Immunodeficiency SyndromeAdherenceAdoptedAdverse effectsAffectAnti-Retroviral AgentsAntiretroviral drug resistanceAntiviral AgentsAntiviral TherapyBaltimoreBindingBinding SitesBiological AssayCapsidCellsDoseDrug resistanceEffectivenessEvaluationEvolutionExhibitsGene ExpressionGenerationsHIVHIV Entry InhibitorsHealthHighly Active Antiretroviral TherapyInfectionIntegrase InhibitorsLaboratoriesLeadLifeLightMeasuresMolecular ConformationMulti-Drug ResistanceNucleosidesPatientsPharmaceutical PreparationsProtease InhibitorProvirusesRegimenRelative (related person)ReportingResistanceShapesSiteStreamTestingViralViral GenesVirusantiretroviral therapychemotherapycompare effectivenesscompliance behaviordrug efficacyinhibitor/antagonistinsightneutralizing antibodynon-nucleoside reverse transcriptase inhibitorspublic health relevancereceptorresearch studyresponsetransmission processvirological synapse
中文摘要
描述(申请人提供):许多艾滋病患者现在可以预期长寿,因为高效抗逆转录病毒疗法(HAART)有效地将艾滋病毒复制抑制到无法检测的水平。然而,化疗伴随着严重的副作用,影响长期健康,费用非常昂贵,因此干扰了患者的依从性。因此,仍有必要开发和优化治疗方案,以减少副作用,促进更好的依从性,并提高相对药物疗效。巴尔的摩和特雷科拉的实验室最近对抗逆转录病毒疗法和艾滋病毒细胞间传播过程中的中和抗体的有效性提出了质疑。细胞间传播允许病毒通过指定的病毒学突触的细胞间接触部位进行有效传播。重要的是,它增加了受感染的靶细胞中的前病毒数量,从而导致更高的病毒基因
与无细胞艾滋病毒感染相比,其表达水平更高。更有效的局部MOI导致感染的高度多样性,这可能导致细胞间传播对抗病毒治疗的抵抗力增加。这些最近的观察需要重新评估常用的抗逆转录病毒疗法,以防止艾滋病毒细胞到细胞的传播。在这里,我们建议系统地测试多种抗逆转录病毒抑制剂对艾滋病毒细胞间传播的有效性。
我们假设,观察到的抗逆转录病毒药物耐药性取决于药物的抑制潜力。具有高抑制潜力的药物可能是最有效的抗艾滋病毒细胞间传播的药物。作为重新评估常用抗逆转录病毒抑制剂有效性的必要的第一步,我们将应用一种高度敏感的定量检测方法来测量HIV细胞间的传播。我们的实验有可能进一步优化现有的HAART方案。
英文摘要
DESCRIPTION (provided by applicant): Many AIDS patients can now expect to live a long life because highly active antiretroviral therapies (HAART) effectively suppress HIV replication to undetectable levels. However, chemotherapy is associated with severe side effects that affect long-term health, is very expensive, and as such interferes with adherence by patients. Therefore, there is a continued need to develop and optimize therapy regimens to lessen side effects, promote better adherence, and increase the relative drug efficacy. The Baltimore and the Trkola laboratories have recently questioned the effectiveness of antiretroviral therapies and neutralizing antibodies during HIV cell-to-cell transmission. Cell-to-cell transmission allows efficient viral spreading via sites of cell-cell contact designated virological synapses. Importanty, it increases the number of proviruses in infected target cells thereby leading to higher viral gene
expression as compared to infections by cell-free HIV. The higher effective local MOI leads to a high multiplicity of infection that can result in the increased resistance of cell-to-cell transmision to antiviral therapies. These recent observations require a re-evaluation of commonly used antiretroviral therapies against HIV cell-to-cell transmission. Here we propose to systematically test the effectiveness of numerous antiretroviral inhibitors against HIV cell-to-cell transmission.
We hypothesize that the observed resistance to anti-retroviral drugs depends on the inhibitory potential of the drug. Drugs with high inhibitory potential may be the most effective against cell-to-cell transmission of HIV. We will apply a highly sensitive and quantitative assay that measures HIV cell- to-cell transmission as a necessary first step to re-evaluate the efficacy of commonly used antiretroviral inhibitors. Our experiments have the potential to further optimize existing HAART regimens.
期刊论文(1)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1371/journal.ppat.1003982
发表时间:
2014-02
期刊:
PLoS pathogens
影响因子:
6.7
作者:
[Agosto LM, Zhong P, Munro J, Mothes W]
通讯作者:
Mothes W
CHEETAH Center for the Structural Biology of HIV Infection, Restriction, and Viral Dynamics
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批准号:10508319
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依托单位:
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海外基金