在临床前动物模型中,在人血浆中通过基于适配体的测量监测HIV抗逆转录病毒治疗

Jing Li, Vincent Clark, Chen-Hsu Yu, Karen Scida, Miguel Aller Pellitero, Rolando L. Albarracín Rivera, Wenrui Zhong, Erin Demek, Jeffrey Fountain, J.D. Mahlum, Richard E. Haaland, Gregory V. Carr, Jonathan Sczepanski, Netzahualcóyotl Arroyo-Currás
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引用次数: 0

摘要

监测抗逆转录病毒药物的浓度对于确保患者遵守艾滋病毒治疗和预防方案至关重要,这对药物疗效至关重要。这些工具也可用于在献血中心筛查样本,以避免潜在的新感染。目前支持抗逆转录病毒药物监测的基准方法是液相色谱-质谱联用(LC-MS),它需要配备昂贵仪器的集中设备,并且血液到结果的周转时间为数天至数周,因此无法进行有效的药物监测。为了克服这一问题,开发了抗逆转录病毒药物恩曲他滨的适体,市场上大多数抗逆转录病毒联合疗法中都有这种药物,用于感染管理和预防。该适体在生物体液中具有临床相关的敏感性,并且相对于胞嘧啶、胞苷、氟胞苷和拉米夫定(又名3TC)等相近的类似物具有高度选择性。利用该适体,开发了两种分析方法,一种用于在啮齿动物研究模型中连续、体内监测恩曲他滨,另一种用于快速、高通量筛选人血浆中恩曲他滨水平。通过盲法分析验证,该临床检测方法与基准LC-MS方法的阳性相关性为86.9%,阴性相关性为100%,总体符合率为95%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Monitoring HIV Antiretroviral Therapy via Aptamer-Based Measurements in Preclinical Animal Models, in Human Plasma

Monitoring HIV Antiretroviral Therapy via Aptamer-Based Measurements in Preclinical Animal Models, in Human Plasma

Monitoring the concentration of antiretroviral drugs is critical to ensuring patient adherence to HIV treatment and prevention regimens, which is crucial for drug efficacy. These tools may also be useful for screening samples at blood donation centers to avert potential new infections. The current benchmark method to support antiretroviral drug monitoring, liquid chromatography coupled to mass spectrometry (LC-MS), requires centralized facilities with costly instrumentation, and has blood-to-result turnaround times of days to weeks, making it impractical for effective drug monitoring. Seeking to overcome this issue, an aptamer is developed for the antiretroviral drug emtricitabine, which is present in most antiretroviral combination therapies in the market and used for both infection management and prevention. The aptamer has clinically relevant sensitivity in biofluids and is highly selective relative to close analogs such as cytosine, cytidine, fluorocytidine, and lamivudine (a.k.a. 3TC). Using this aptamer, two analytical assays are developed, one for continuous, in-vivo emtricitabine monitoring in rodent research models, and one for rapid and high-throughput screening of emtricitabine levels in human plasma. Through blinded analytical validation, this clinical assay achieved an 86.9% positive and 100% negative correlation, with an overall agreement rate of 95% relative to the benchmark LC-MS method.

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