Department of Pediatrics, David Geffen School of Medicine, University of California, Los Angeles.
Office of the Global AIDS Coordinator and Health Diplomacy, US Department of State, Washington D.C.
Clin Infect Dis. 2018 May 17;66(11):1770-1777. doi: 10.1093/cid/cix1104.
BACKGROUND: The presence of antiretroviral drug-associated resistance mutations (DRMs) may be particularly problematic in human immunodeficiency virus (HIV)-infected pregnant women as it can lead to mother-to-child transmission (MTCT) of resistant HIV strains. This study evaluated the prevalence and the effect of antiretroviral DRMs in previously untreated mother-infant pairs. METHODS: A case-control design of 1:4 (1 transmitter to 4 nontransmitters) was utilized to evaluate DRMs as a predictor of HIV MTCT in specimens obtained from mother-infant pairs. ViroSeq HIV-1 genotyping was performed on mother-infant specimens to assess for clinically relevant DRMs. RESULTS: One hundred forty infants acquired HIV infection; of these, 123 mother-infant pairs (88%) had specimens successfully amplified using ViroSeq and assessed for drug resistance genotyping. Additionally, 483 of 560 (86%) women who did not transmit HIV to infants also had samples evaluated for DRMs. Sixty-three of 606 (10%) women had clinically relevant DRMs; 12 (2%) had DRMs against >1 drug class. Among 123 HIV-infected infants, 13 (11%) had clinically relevant DRMs, with 3 (2%) harboring DRMs against >1 drug class. In univariate and multivariate analyses, DRMs in mothers were not associated with increased HIV MTCT (adjusted odds ratio, 0.8 [95% confidence interval, .4-1.5]). Presence of DRMs in transmitting mothers was strongly associated with DRM presence in their infants (P < .001). CONCLUSIONS: Preexisting DRMs were common in untreated HIV-infected pregnant women, but did not increase the risk of HIV MTCT. However, if women with DRMs are not virologically suppressed, they may transmit resistant mutations, thus complicating infant management.
背景:抗逆转录病毒药物相关耐药突变(DRMs)的存在可能在感染人类免疫缺陷病毒(HIV)的孕妇中尤为成问题,因为它可能导致耐药 HIV 株的母婴传播(MTCT)。本研究评估了未经治疗的母婴对 HIV 感染的耐药突变的流行率和影响。
方法:采用 1:4(1 个传播者对 4 个非传播者)的病例对照设计,评估了耐药突变作为母婴传播 HIV 的预测因子。从母婴对中获取标本,使用 ViroSeq HIV-1 基因分型来评估临床相关的耐药突变。
结果:140 名婴儿感染了 HIV;其中,123 对母婴对(88%)有标本成功使用 ViroSeq 扩增并进行了耐药基因分型评估。此外,483 名未将 HIV 传播给婴儿的女性中有 483 名(86%)也对耐药突变进行了评估。63 名女性(10%)有临床相关的耐药突变;12 名(2%)对超过 1 种药物类别有耐药突变。在 123 名 HIV 感染的婴儿中,13 名(11%)有临床相关的耐药突变,其中 3 名(2%)对超过 1 种药物类别有耐药突变。在单变量和多变量分析中,母亲的耐药突变与增加的 HIV MTCT 无关(调整后的优势比,0.8 [95%置信区间,0.4-1.5])。传播母亲的耐药突变与婴儿耐药突变的存在有很强的相关性(P <.001)。
结论:未经治疗的 HIV 感染孕妇中,预先存在的耐药突变很常见,但并未增加 HIV MTCT 的风险。然而,如果有耐药突变的女性没有病毒学抑制,她们可能会传播耐药突变,从而使婴儿的管理复杂化。
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