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多替拉韦、替诺福韦、拉米夫定和依非韦伦在多个中枢神经系统区室中的死后分析

Postmortem Analysis of Dolutegravir, Tenofovir, Lamivudine, and Efavirenz Penetration in Multiple Central Nervous System Compartments.

作者信息

Wang Fan, Rademeyer Kara, Namuju Olivie C, Abdusalaamu Kizito, Fisher James, Meya David B, McRae MaryPeace, Boulware David R, Lukande Robert, Nicol Melanie R

机构信息

Department of Experimental and Clinical Pharmacology, University of Minnesota, Minneapolis, Minnesota, USA.

Department of Pharmacotherapy and Outcomes Sciences, Virginia Commonwealth University, Richmond, Virginia, USA.

出版信息

J Infect Dis. 2024 Nov 15;230(5):1215-1223. doi: 10.1093/infdis/jiae325.

Abstract

BACKGROUND

Central nervous system (CNS) compartmentalization provides opportunity for human immunodeficiency virus (HIV) persistence and resistance development. Differences between cerebrospinal fluid (CSF) and cerebral matter regarding HIV persistence are well described. However, CSF is often used as surrogate for CNS drug exposure, and knowledge from solid brain tissue is rare.

METHODS

Dolutegravir, tenofovir, lamivudine, and efavirenz concentrations were measured across 13 CNS regions plus plasma in samples collected during autopsy in 49 Ugandan decedents. Median time from death to autopsy was 8 hours (interquartile range, 5-15 hours). To evaluate postmortem redistribution, a time course study was performed in a mouse model.

RESULTS

Regions with the highest penetration ratios were choroid plexus/arachnoid (dolutegravir and tenofovir), CSF (lamivudine), and cervical spinal cord/meninges (efavirenz); the lowest were corpus callosum (dolutegravir and tenofovir), frontal lobe (lamivudine), and parietal lobe (efavirenz). On average, brain concentrations were 84%, 87%, and 76% of CSF for dolutegravir, tenofovir, and lamivudine, respectively. Postmortem redistribution was observed in the mouse model, with tenofovir and lamivudine concentration increased by 350% and efavirenz concentration decreased by 24% at 24 hours postmortem.

CONCLUSIONS

Analysis of postmortem tissue provides a unique opportunity to investigate CNS antiretroviral penetration. Regional differences were observed paving the way to identify mechanisms of viral compartmentalization and/or neurotoxicity.

摘要

背景

中枢神经系统(CNS)的分隔为人类免疫缺陷病毒(HIV)的持续存在和耐药性发展提供了机会。脑脊液(CSF)与脑实质在HIV持续存在方面的差异已有充分描述。然而,CSF常被用作中枢神经系统药物暴露的替代指标,而来自实体脑组织的知识却很少。

方法

在49名乌干达死者尸检期间采集的样本中,测量了13个中枢神经系统区域以及血浆中的多替拉韦、替诺福韦、拉米夫定和依非韦伦浓度。从死亡到尸检的中位时间为8小时(四分位间距,5 - 15小时)。为评估死后再分布,在小鼠模型中进行了一项时间进程研究。

结果

穿透率最高的区域是脉络丛/蛛网膜(多替拉韦和替诺福韦)、脑脊液(拉米夫定)和颈脊髓/脑膜(依非韦伦);最低的是胼胝体(多替拉韦和替诺福韦)、额叶(拉米夫定)和顶叶(依非韦伦)。平均而言,多替拉韦、替诺福韦和拉米夫定的脑浓度分别为脑脊液浓度的84%、87%和76%。在小鼠模型中观察到了死后再分布,死后24小时时替诺福韦和拉米夫定浓度增加了350%,依非韦伦浓度降低了24%。

结论

对死后组织的分析为研究中枢神经系统抗逆转录病毒药物的穿透提供了独特的机会。观察到的区域差异为确定病毒分隔和/或神经毒性机制铺平了道路。

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