Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA.
Department of Pediatrics.
J Acquir Immune Defic Syndr. 2021 Dec 1;88(4):361-365. doi: 10.1097/QAI.0000000000002771.
Pregnant women using antiretrovirals (ARVs) may have persistent vaginal viral shedding, which could be associated with sexual and perinatal HIV transmission. However, there are scant data on vaginal viral load (VVL) in pregnant women with undetectable plasma viral load (PVL).
This study was a post hoc analysis of an open-label randomized trial to evaluate the virologic response of 2 ART regimens. The participants were ART-naive women living with HIV initiating ART regimens between 20 and 36 weeks of pregnancy recruited at 19 clinical sites in 6 countries. Participants were randomized to receive 400 mg of raltegravir 2 times a day or 600 mg of efavirenz 4 times a day in addition to 150 mg of lamivudine and 300 mg of zidovudine 2 times a day. VVL and PVL tests were performed at every study visit. The primary outcome measures were HIV-1 PVL and VVL at maternal study week 4 and rates of perinatal HIV transmission.
A total of 408 were enrolled, of whom 323 had VVL samples 4 weeks after enrollment and were included in this analysis. Among women with undetectable/nonquantifiable PVL during ART, the overall rate of quantifiable VVL at week 4 was 2.54% (7/275). Of the 275 with nonquantifiable PVL, 99.1% (115/116) and 96.2% (153/159) had nonquantifiable VVL in the efavirenz and raltegravir arms, respectively. None of the 7 women with quantifiable VVL at the week 4 study visit transmitted HIV to their infants.
Detectable VVL in pregnant women with undetectable/nonquantifiable PVL while receiving ART was rare and not associated with perinatal HIV transmission.
使用抗逆转录病毒药物(ARV)的孕妇可能存在持续性阴道病毒脱落,这可能与性传播和围产期 HIV 传播有关。然而,关于血浆病毒载量(PVL)不可检测的孕妇阴道病毒载量(VVL)的数据很少。
这是一项评估两种 ART 方案病毒学反应的开放标签随机试验的事后分析。参与者为在 6 个国家的 19 个临床站点接受 HIV 治疗的、初次接受 ART 方案的妊娠 20-36 周的妇女。参与者被随机分配接受每天 2 次 400mg 拉替拉韦或每天 4 次 600mg 依非韦伦,外加每天 2 次 150mg 拉米夫定和 300mg 齐多夫定。在每次研究访视时进行 VVL 和 PVL 检测。主要结局指标为母亲研究周 4 时的 HIV-1 PVL 和 VVL 以及围产期 HIV 传播率。
共纳入 408 例患者,其中 323 例在入组后 4 周时具有 VVL 样本,纳入本分析。在 ART 期间 PVL 不可检测/无法定量的妇女中,第 4 周时可定量 VVL 的总体发生率为 2.54%(275 例中有 7 例)。在 275 例 PVL 无法定量的患者中,依非韦伦和拉替拉韦组分别有 99.1%(115/116)和 96.2%(153/159)的患者 VVL 无法定量。在第 4 周研究访视时,7 例可定量 VVL 的患者均未将 HIV 传播给婴儿。
在接受 ART 的不可检测/无法定量 PVL 的孕妇中,可检测到的 VVL 很少见,且与围产期 HIV 传播无关。