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在长效卡博特韦用于HIV预防背景下感染HIV者的HIV DNA水平:来自HPTN 083和084的病例分析

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.

作者信息

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

机构信息

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

出版信息

AIDS Res Hum Retroviruses. 2025 Jan;41(1):30-36. doi: 10.1089/aid.2024.0049. Epub 2024 Oct 28.

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 <LLOD; one near the LLOD (4.2 copies/10 PBMCs); in 2/4 cases, the DNA level was still <10 copies/10 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/10 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.

摘要

我们在HPTN 083和084试验中,对接受长效卡博特韦(CAB-LA)或替诺福韦酯/恩曲他滨(TDF/FTC)暴露前预防且进行了HIV DNA检测以帮助确定HIV状态的个体,评估了其HIV DNA水平。HIV DNA检测使用在研究站点获得HIV检测反应性结果后采集的外周血单个核细胞(PBMC)样本进行。使用液滴数字PCR对DNA进行定量(检测下限[LLOD]:4.09拷贝/百万PBMC)。最终的HIV状态以及首次HIV阳性就诊的时间由独立判定委员会根据实时现场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名HIV阳性(CAB-LA组7名,TDF/FTC组14名)和112名HIV阴性;每人进行1 - 6次检测]。对于HIV感染者,首次HIV阳性就诊与采集用于DNA检测的首个样本之间的时间,接受CAB-LA者的中位数为81天(范围41 - 246天),接受TDF/FTC者为11天(范围3 - 127天)。7例CAB-LA感染病例中有4例(57.1%)初始DNA结果较低[3例检测结果<LLOD;1例接近LLOD(4.2拷贝/10 PBMC);在2/4的病例中,首次HIV阳性就诊后≥40周时DNA水平仍<10拷贝/10 PBMC]。相比之下,TDF/FTC病例中只有3/14(21.4%)初始DNA检测结果较低或为阴性(1例未检测到;2例<10拷贝/10 PBMC)。在本研究中,CAB-LA病例首次HIV阳性就诊与首次DNA检测之间的时间比TDF/FTC病例更长。尽管存在这一差异,但在CAB-LA病例中更频繁地观察到低或不可检测的DNA水平。这表明CAB-LA暴露可能会在早期感染中限制HIV储存库的播种。

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