Department of Global Health, University of Washington, 908 Jefferson Street, Seattle, WA, 98104, USA.
Department of Epidemiology, University of Washington, 3980 15th Ave NE, Seattle, WA, 98195, USA.
Curr HIV/AIDS Rep. 2024 Oct;21(5):264-281. doi: 10.1007/s11904-024-00705-0. Epub 2024 Aug 9.
Adherence-concentration-efficacy benchmarks have not been fully characterized for cisgender women using emtricitabine/tenofovir disoproxil fumarate (FTC/TDF) oral daily pre-exposure prophylaxis (PrEP) for HIV prevention.
We conducted a systematic review to investigate current evidence on the adherence-concentration-efficacy relationship of tenofovir-diphosphate (TFV-DP) derived from FTC/TDF PrEP in dried blood spots (DBS) and peripheral mononuclear cells (PBMC) in cisgender women without HIV, including during pregnancy. We searched for completed and ongoing studies published before May 2024 in PubMed, Embase, Cochrane Library, CINAHL, and clinicaltrial.gov. Overall, 11 studies assessing adherence benchmarks focusing on (n = 5) or involving (n = 6) cisgender women were included. Women-specific median steady-state TFV-DP concentration for daily dosing ranged from 17 to 51 fmol/10 in PBMC and 1389 to 1685 fmol/punch in DBS in non-pregnant women; 50 to 71 fmol/10 in PBMC and 583 to 965 fmol/punch in DBS in pregnant women; and 618 to 1406 fmol/punch in DBS in postpartum women. DBS TFV-DP levels were 14-43% lower in pregnancy versus postpartum or non-pregnant periods, but PBMC TFV-DP levels appear to be comparable. Clinical and modeling studies demonstrate effective HIV protection for women taking at least four doses/week of oral TDF-based PrEP, and emerging evidence suggests that systemic drug levels are more likely to be predictive of efficacy than local tissue levels at the site of exposure. The preponderance of emerging evidence points to comparable efficacy and similar adherence requirement for women as men among those with detectable drug levels, although there was an indication that the highest achievable efficacy may be reached at a lower adherence level in men than women. In this review, we found evidence that women-specific TFV-DP adherence benchmarks in DBS and PBMC are within range of US-based historical thresholds derived from healthy men and women. Emerging evidence suggests that imperfect but adequate adherence to oral FTC/TDF PrEP with at least four doses/week provides sufficient HIV protection in cisgender women as it does in MSM, but more data are still needed to refine intrinsic achievable efficacy estimates for cisgender women.
目前尚未充分确定使用恩曲他滨/替诺福韦二吡呋酯(FTC/TDF)口服每日暴露前预防(PrEP)进行艾滋病毒预防的顺性别女性的依从性-浓度-疗效基准。
我们进行了一项系统评价,以调查目前关于在没有艾滋病毒的顺性别女性中,从 FTC/TDF PrEP 中获得的替诺福韦二磷酸(TFV-DP)在干血斑(DBS)和外周单核细胞(PBMC)中的依从性-浓度-疗效关系的现有证据,包括在怀孕期间。我们在 PubMed、Embase、Cochrane 图书馆、CINAHL 和 clinicaltrial.gov 中搜索了截至 2024 年 5 月之前发表的已完成和正在进行的研究。总体而言,纳入了 11 项评估依从性基准的研究,这些研究主要关注(n=5)或涉及(n=6)顺性别女性。非妊娠女性中,每日剂量的 PBMC 中女性特异性稳态 TFV-DP 浓度范围为 17 至 51 fmol/10,DBS 中为 1389 至 1685 fmol/冲;妊娠女性中 PBMC 中为 50 至 71 fmol/10,DBS 中为 583 至 965 fmol/冲;产后女性中 DBS 中为 618 至 1406 fmol/冲。与产后或非妊娠期相比,妊娠期间 DBS TFV-DP 水平降低了 14-43%,但 PBMC TFV-DP 水平似乎相当。临床和建模研究表明,每周至少服用四剂口服 TDF 为基础的 PrEP 的女性具有有效的艾滋病毒保护作用,而新出现的证据表明,全身药物水平比暴露部位的局部组织水平更有可能预测疗效。越来越多的证据表明,在有可检测药物水平的人群中,女性的疗效与男性相当,且需要相似的依从性要求,尽管有迹象表明男性达到最高可实现疗效的依从性水平可能低于女性。在本综述中,我们发现证据表明,DBS 和 PBMC 中女性特异性 TFV-DP 依从性基准在基于美国的健康男性和女性中得出的历史阈值范围内。新出现的证据表明,每周至少服用四剂口服 FTC/TDF PrEP,即使依从性不完美,但仍足以在顺性别女性中提供足够的艾滋病毒保护,这与男男性行为者中的情况相同,但仍需要更多数据来细化顺性别女性的内在可实现疗效估计。