HIV DNA Levels in Persons Who Acquired HIV in the Setting of Long-Acting Cabotegravir for HIV Prevention: Analysis of Cases from HPTN 083 and 084.

IF 1.5 4区 医学 Q4 IMMUNOLOGY
Jessica M Fogel, Deborah Persaud, Estelle Piwowar-Manning, Paul Richardson, Joseph Szewczyk, Mark A Marzinke, Zhe Wang, Xu Guo, Marybeth McCauley, Jennifer Farrior, Ha Viet Tran, Chaiwat Ungsedhapand, Carrie-Anne Mathew, Juliet Mpendo, Alex R Rinehart, James F Rooney, Myron S Cohen, Brett Hanscom, Beatriz Grinsztejn, Mina C Hosseinipour, Sinead Delany-Moretlwe, Raphael J Landovitz, Susan H Eshleman
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引用次数: 0

Abstract

We evaluated HIV DNA levels in individuals who received long-acting cabotegravir (CAB-LA) or tenofovir disoproxil fumarate/emtricitabine (TDF/FTC) pre-exposure prophylaxis in the HPTN 083 and 084 trials and had HIV DNA testing performed to help determine HIV status. HIV DNA testing was performed using peripheral blood mononuclear cell (PBMC) samples collected after a reactive HIV test was obtained at a study site. DNA was quantified using droplet digital PCR (lower limit of detection [LLOD]: 4.09 copies/million PBMCs). Final HIV status and the timing of the first HIV-positive visit were determined by an independent adjudication committee based on HIV test results from real-time site testing and retrospective testing at a centralized laboratory. HIV DNA testing was performed for 133 participants [21 HIV-positive (7 CAB-LA arm, 14 TDF/FTC arm) and 112 HIV-negative; 1-6 tests/person]. For persons with HIV, the time between the first HIV-positive visit and collection of the first sample for DNA testing was a median of 81 days for those receiving CAB-LA (range 41-246) and 11 days for those receiving TDF/FTC (range 3-127). Four (57.1%) of the seven CAB-LA cases with infection had a low initial DNA result [three detected 6 PBMCs); in 2/4 cases, the DNA level was still <10 copies/106 PBMCs ≥40 weeks after the first HIV-positive visit. In contrast, only 3/14 (21.4%) of the TDF/FTC cases had a low or negative initial DNA test result (one not detected; two <10 copies/106 PBMCs). In this study, the time between the first HIV-positive visit and the first DNA test was longer in the CAB-LA cases than the TDF/FTC cases. Despite this difference, low or undetectable DNA levels were more frequently observed in the CAB-LA cases. This suggests that CAB-LA exposure may limit seeding of the HIV reservoir in early infection.

在使用长效卡博特拉韦预防艾滋病的情况下,感染艾滋病病毒者的艾滋病毒 DNA 水平:HPTN 083 和 084 病例分析。
我们评估了在 HPTN 083 和 084 试验中接受长效卡博替拉韦(CAB-LA)或替诺福韦酯/恩曲他滨(TDF/FTC)暴露前预防治疗并进行 HIV DNA 检测以帮助确定 HIV 感染状况的患者体内的 HIV DNA 水平。HIV DNA 检测使用的是在研究机构获得反应性 HIV 检测结果后收集的外周血单核细胞 (PBMC) 样本。使用液滴数字 PCR 对 DNA 进行量化(检测下限 [LLOD]:4.09 拷贝/百万 PBMCs)。最终的 HIV 感染状况和首次 HIV 阳性就诊时间由独立评审委员会根据现场实时检测和集中实验室回顾性检测的 HIV 检测结果确定。对 133 名参与者进行了 HIV DNA 检测[21 人 HIV 阳性(7 人 CAB-LA 试验组,14 人 TDF/FTC 试验组),112 人 HIV 阴性;1-6 次检测/人]。对于 HIV 感染者,接受 CAB-LA 治疗的患者从 HIV 阳性首次就诊到 DNA 检测首次样本采集的时间中位数为 81 天(41-246 天不等),接受 TDF/FTC 治疗的患者为 11 天(3-127 天不等)。在 7 例 CAB-LA 感染病例中,有 4 例(57.1%)的初始 DNA 结果较低(3 例检测到 6 个 PBMCs);在 2/4 例病例中,在首次 HIV 阳性就诊≥40 周后,DNA 水平仍为 6 个 PBMCs。相比之下,只有 3/14 例(21.4%)TDF/FTC 病例的初始 DNA 检测结果为低或阴性(1 例未检测到;2 例检测到 6 PBMCs)。在本研究中,CAB-LA 病例从首次 HIV 阳性就诊到首次 DNA 检测的时间比 TDF/FTC 病例长。尽管存在这种差异,但在 CAB-LA 病例中更常观察到 DNA 水平较低或检测不到。这表明,CAB-LA 的暴露可能会在早期感染中限制 HIV 储库的播种。
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来源期刊
CiteScore
3.10
自引率
6.70%
发文量
201
审稿时长
3-6 weeks
期刊介绍: AIDS Research and Human Retroviruses was the very first AIDS publication in the field over 30 years ago, and today it is still the critical resource advancing research in retroviruses, including AIDS. The Journal provides the broadest coverage from molecular biology to clinical studies and outcomes research, focusing on developments in prevention science, novel therapeutics, and immune-restorative approaches. Cutting-edge papers on the latest progress and research advances through clinical trials and examination of targeted antiretroviral agents lead to improvements in translational medicine for optimal treatment outcomes. AIDS Research and Human Retroviruses coverage includes: HIV cure research HIV prevention science - Vaccine research - Systemic and Topical PreP Molecular and cell biology of HIV and SIV Developments in HIV pathogenesis and comorbidities Molecular biology, immunology, and epidemiology of HTLV Pharmacology of HIV therapy Social and behavioral science Rapid publication of emerging sequence information.
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