Naicker Cherise L, Mansoor Leila E, Dawood Halima, Naidoo Kogieleum, Singo Denzhe, Matten David, Williamson Carolyn, Abdool Karim Quarraisha
Centre for the AIDS Programme of Research in South Africa (CAPRISA), University of KwaZulu-Natal, Durban, South Africa.
MRC-CAPRISA HIV-TB Pathogenesis and Treatment Research Unit, University of KwaZulu-Natal, Durban, South Africa.
BMC Infect Dis. 2020 Jul 22;20(1):532. doi: 10.1186/s12879-020-05255-5.
The World Health Organisation recommends the use of tenofovir-containing pre-exposure prophylaxis (PrEP) as an additional Human Immunodeficiency Virus (HIV) prevention choice for men and women at substantial risk of HIV infection. PrEP could fill an important HIV prevention gap, especially for sexually active young women who are limited in their ability to negotiate mutual monogamy or condom use. As PrEP is scaled up in high HIV incidence settings, it is crucial to consider the importance of early identification of HIV infection during PrEP use, to allow for rapid discontinuation of PrEP to reduce the risk of antiretroviral (ARV) resistance. The purpose of this case study is to provide this critical evidence.
This report describes a 20-year-old woman in a HIV sero-discordant relationship who initiated oral PrEP (tenofovir disoproxil fumarate (TDF) and emtricitabine (FTC)) through a demonstration project (CAPRISA 084) in October 2017. Despite good adherence throughout her PrEP use, she tested HIV antibody positive at month nine of study participation. Retrospective testing showed increasing HIV viral load over time, and retrospective use of fourth-generation rapid HIV tests showed HIV detection (positive antigen/antibody) at month one. Sequencing confirmed a dominant wild type at month one with dual therapy resistance patterns emerging by month three (M184V and K65R mutations), which is suggestive of protracted PrEP use during an undetected HIV infection. The participant was referred to infectious diseases for further management of her HIV infection and was initiated on a first line, tenofovir-sparing regimen. At the time of this report (January 2020), the participant had been on ARV- therapy (ART) for 13 months and had no signs of either clinical, immunologic or virologic failure.
This case report highlights the importance of appropriate HIV screening during wider oral PrEP scale-up in high HIV incidence settings to circumvent the consequences of prolonged dual therapy in an undiagnosed HIV infection and in turn prevent ARV resistance.
世界卫生组织建议,对于感染人类免疫缺陷病毒(HIV)风险较高的男性和女性,使用含替诺福韦的暴露前预防(PrEP)作为额外的HIV预防选择。PrEP可以填补重要的HIV预防空白,特别是对于性活跃的年轻女性,她们在协商实行相互一夫一妻制或使用避孕套方面能力有限。随着PrEP在HIV高发病率地区的推广,在使用PrEP期间早期识别HIV感染至关重要,以便迅速停用PrEP以降低抗逆转录病毒(ARV)耐药性风险。本病例研究的目的是提供这一关键证据。
本报告描述了一名20岁女性,处于HIV血清学不一致关系中,她于2017年10月通过一个示范项目(CAPRISA 084)开始口服PrEP(富马酸替诺福韦二吡呋酯(TDF)和恩曲他滨(FTC))。尽管在整个PrEP使用过程中依从性良好,但在参与研究的第9个月她的HIV抗体检测呈阳性。回顾性检测显示HIV病毒载量随时间增加,回顾性使用第四代HIV快速检测显示在第1个月检测到HIV(抗原/抗体阳性)。测序证实第1个月时为优势野生型,到第3个月出现双重治疗耐药模式(M184V和K65R突变),这表明在未检测到的HIV感染期间长期使用PrEP。该参与者被转诊至传染病科进一步管理其HIV感染,并开始使用一线的不含替诺福韦的治疗方案。在本报告发布时(2020年1月),该参与者接受抗逆转录病毒治疗(ART)已13个月,没有临床、免疫或病毒学失败的迹象。
本病例报告强调了在HIV高发病率地区更广泛地推广口服PrEP期间进行适当HIV筛查的重要性,以规避在未诊断的HIV感染中延长双重治疗的后果,进而预防ARV耐药性。