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Sci Transl Med. 2019 Aug 7;11(504). doi: 10.1126/scitranslmed.aav5685.
2
Predictions of time to HIV viral rebound following ART suspension that incorporate personal biomarkers.预测 ART 停药后 HIV 病毒反弹的时间,需要纳入个人生物标志物。
PLoS Comput Biol. 2019 Jul 24;15(7):e1007229. doi: 10.1371/journal.pcbi.1007229. eCollection 2019 Jul.
3
Recommendations for analytical antiretroviral treatment interruptions in HIV research trials-report of a consensus meeting.抗逆转录病毒治疗中断分析在 HIV 研究试验中的建议——共识会议报告。
Lancet HIV. 2019 Apr;6(4):e259-e268. doi: 10.1016/S2352-3018(19)30052-9. Epub 2019 Mar 15.
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Antibody and TLR7 agonist delay viral rebound in SHIV-infected monkeys.抗体和 TLR7 激动剂可延缓感染 SHIV 的猴子体内病毒反弹。
Nature. 2018 Nov;563(7731):360-364. doi: 10.1038/s41586-018-0600-6. Epub 2018 Oct 3.
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The size of the expressed HIV reservoir predicts timing of viral rebound after treatment interruption.所表达的HIV储存库的大小可预测治疗中断后病毒反弹的时间。
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Immunological biomarkers predict HIV-1 viral rebound after treatment interruption.免疫生物标志物可预测治疗中断后HIV-1病毒反弹。
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The need for treatment interruption studies and biomarker identification in the search for an HIV cure.在寻找治愈艾滋病方法的过程中进行治疗中断研究和生物标志物识别的必要性。
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Proc Natl Acad Sci U S A. 2015 Mar 10;112(10):E1126-34. doi: 10.1073/pnas.1414926112. Epub 2015 Feb 23.
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Posttreatment controllers: what do they tell us?治疗后病情控制者:他们能告诉我们什么?
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一种用于治疗中断后HIV病毒载量反弹的灵活非线性混合效应模型。

A flexible nonlinear mixed effects model for HIV viral load rebound after treatment interruption.

作者信息

Wang Rui, Bing Ante, Wang Cathy, Hu Yuchen, Bosch Ronald J, DeGruttola Victor

机构信息

Department of Population Medicine, Harvard Pilgrim Health Care Institute and Harvard Medical School, Boston, Massachusetts, USA.

Department of Biostatistics, Harvard T. H. Chan School of Public Health, Boston, Massachusetts, USA.

出版信息

Stat Med. 2020 Jul 10;39(15):2051-2066. doi: 10.1002/sim.8529. Epub 2020 Apr 15.

DOI:10.1002/sim.8529
PMID:32293756
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8081565/
Abstract

Characterization of HIV viral rebound after the discontinuation of antiretroviral therapy is central to HIV cure research. We propose a parametric nonlinear mixed effects model for the viral rebound trajectory, which often has a rapid rise to a peak value followed by a decrease to a viral load set point. We choose a flexible functional form that captures the shapes of viral rebound trajectories and can also provide biological insights regarding the rebound process. Each parameter can incorporate a random effect to allow for variation in parameters across individuals. Key features of viral rebound trajectories such as viral set points are represented by the parameters in the model, which facilitates assessment of intervention effects and identification of important pretreatment interruption predictors for these features. We employ a stochastic expectation-maximization (StEM) algorithm to incorporate HIV-1 RNA values that are below the lower limit of assay quantification. We evaluate the performance of our model in simulation studies and apply the proposed model to longitudinal HIV-1 viral load data from five AIDS Clinical Trials Group treatment interruption studies.

摘要

抗逆转录病毒治疗中断后HIV病毒反弹的特征描述是HIV治愈研究的核心。我们提出了一种用于病毒反弹轨迹的参数化非线性混合效应模型,该轨迹通常会迅速上升至峰值,随后下降至病毒载量设定点。我们选择了一种灵活的函数形式,它能够捕捉病毒反弹轨迹的形状,还能提供有关反弹过程的生物学见解。每个参数都可以纳入随机效应,以考虑个体间参数的变化。病毒反弹轨迹的关键特征(如病毒设定点)由模型中的参数表示,这有助于评估干预效果,并识别这些特征的重要治疗前中断预测因素。我们采用随机期望最大化(StEM)算法来纳入低于检测定量下限的HIV-1 RNA值。我们在模拟研究中评估了模型的性能,并将所提出的模型应用于来自五项艾滋病临床试验组治疗中断研究的纵向HIV-1病毒载量数据。