Walters Magdalene K, Bulterys Michelle A, Barry Michael, Hicks Sarah, Richey Ann, Sabin Margalit, Louden Diana, Mahy Mary, Stover John, Glaubius Robert, Kyu Hmwe H, Boily Marie-Claude, Mofenson Lynne, Powis Kathleen, Imai-Eaton Jeffrey W
MRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.
Department of Epidemiology, School of Public Health, University of Washington, Seattle, WA, USA; Herbert Wertheim School of Public Health, University of California San Diego, La Jolla, CA, USA.
Lancet HIV. 2025 Sep;12(9):e638-e648. doi: 10.1016/S2352-3018(25)00132-8. Epub 2025 Jul 31.
Eliminating HIV vertical transmission is a global priority and monitored by estimating paediatric HIV infections with the UNAIDS-supported Spectrum AIDS Impact Module (Spectrum-AIM). Recent innovations in antiretroviral therapy (ART) service-delivery models and first-line regimens aimed to reduce vertical transmission probabilities. We did a systematic review and meta-analysis to estimate vertical transmission probabilities by maternal immunological and treatment status.
In this systematic review and meta-regression, we combined an updated systematic review with previous data in meta-regression models to estimate vertical transmission probabilities and determinants. We searched PubMed, Embase, the Global Health Database, WHO Global Index Medicus, CINAHL Complete, and Cochrane CENTRAL for peer-reviewed English-language studies from all regions published between Jan 1, 2018 and Feb 8, 2024, with search term domains mentioning "HIV", "transmission", "perinatal", and "breastfeeding periods", and "infants born to women living with HIV" or related terms from randomised trials, cohort studies, or observational studies. Four meta-regression models estimated vertical transmission probabilities. We assessed model sensitivity and compared estimates to Spectrum-AIM's previous results. Finally, we fit a meta-regression model to assess the association of ART class and initiation timing on viral load suppression (VLS) at delivery.
Of 12 588 potential studies, we identified 24 new studies, which along with the 86 from previous reviews yielded 110 total studies included in meta-regression analysis. For women not receiving ART, higher CD4 count was associated with lower odds of perinatal vertical transmission (odds ratio [OR] 0·80, 95% CI 0·75-0·84, per 100 cells per μL increase). For pregnant women on ART, each additional week on ART before delivery reduced odds of vertical transmission by 5·6% (95% CI 4·2-7·0). The OR of perinatal vertical transmission among pregnant women initiating integrase inhibitor-based ART 20 weeks before delivery was 0·36 (0·14-0·94) compared with those initiating non-nucleoside reverse transcriptase inhibitor (NNRTI)-based ART. This association was confounded by study region. Odds of VLS were lower when ART was initiated late in pregnancy (OR 0·37, 0·21-0·68) for the reference regimen [NNRTI]), without significant difference by ART regimen.
Vertical transmission probability varies by maternal immunological stage, treatment regimen, and timing of treatment initiation. These estimates have been incorporated into Spectrum-AIM for UNAIDS 2025 HIV estimates. Earlier ART initiation is associated with higher odds of VLS at delivery. Further evidence is needed on the effects of recent ART innovations on vertical transmission outcomes.
National Institutes of Health, UNAIDS, and UK Research and Innovation.
消除艾滋病毒垂直传播是一项全球优先事项,通过使用联合国艾滋病规划署支持的“频谱艾滋病影响模块”(Spectrum - AIM)估计儿童艾滋病毒感染情况进行监测。抗逆转录病毒疗法(ART)服务提供模式和一线治疗方案的最新创新旨在降低垂直传播概率。我们进行了一项系统评价和荟萃分析,以根据孕产妇免疫和治疗状况估计垂直传播概率。
在这项系统评价和荟萃回归中,我们将更新后的系统评价与荟萃回归模型中的先前数据相结合,以估计垂直传播概率及其决定因素。我们在PubMed、Embase、全球卫生数据库、世界卫生组织全球医学索引、CINAHL Complete和Cochrane CENTRAL中检索了2018年1月1日至2024年2月8日期间所有地区发表的经同行评审的英文研究,检索词领域提及“艾滋病毒”“传播”“围产期”“哺乳期”以及“感染艾滋病毒的妇女所生婴儿”或来自随机试验、队列研究或观察性研究的相关术语。四个荟萃回归模型估计垂直传播概率。我们评估了模型敏感性,并将估计结果与Spectrum - AIM的先前结果进行比较。最后,我们拟合了一个荟萃回归模型,以评估ART类别和开始时间与分娩时病毒载量抑制(VLS)之间的关联。
在12588项潜在研究中,我们确定了24项新研究,这些研究与先前综述中的86项研究一起,共有110项研究纳入荟萃回归分析。对于未接受ART的女性,较高的CD4细胞计数与围产期垂直传播几率较低相关(比值比[OR]为0.80,95%置信区间为0.75 - 0.84,每增加100个细胞/μL)。对于接受ART的孕妇,分娩前每多接受一周ART,垂直传播几率降低5.6%(95%置信区间为4.2 - 7.0)。与开始基于非核苷类逆转录酶抑制剂(NNRTI)的ART的孕妇相比,在分娩前20周开始基于整合酶抑制剂的ART的孕妇围产期垂直传播的OR为0.36(0.14 - 0.94)。这种关联受研究地区的影响。对于参考治疗方案[NNRTI]),在妊娠晚期开始ART时VLS的几率较低(OR为0.37,0.21 - 0.68),不同ART方案之间无显著差异。
垂直传播概率因孕产妇免疫阶段、治疗方案和治疗开始时间而异。这些估计值已纳入Spectrum - AIM,用于联合国艾滋病规划署2025年艾滋病毒估计。更早开始ART与分娩时VLS几率较高相关。需要更多证据证明近期ART创新对垂直传播结果的影响。
美国国立卫生研究院、联合国艾滋病规划署和英国研究与创新署