Centre for Respiratory Diseases Research, Kenya Medical Research Institute, Nairobi, Kenya.
Department of Global Health, University of Washington, Seattle, Washington.
Pediatr Infect Dis J. 2024 Mar 1;43(3):250-256. doi: 10.1097/INF.0000000000004190. Epub 2023 Nov 22.
The effect of maternal HIV on infant Mycobacterium tuberculosis (Mtb) infection risk is not well-characterized.
Pregnant women with/without HIV and their infants were enrolled in a longitudinal cohort in Kenya. Mothers had interferon gamma-release assays (QFT-Plus) and tuberculin skin tests (TST) at enrollment in pregnancy; children underwent TST at 12 and 24 months of age. We estimated the incidence and correlates of infant TST-positivity using Cox proportional hazards regression.
Among 322 infants, 170 (53%) were HIV-exposed and 152 (47%) were HIV-unexposed. Median enrollment age was 6.6 weeks [interquartile range (IQR): 6.1-10.0]; most received Bacillus Calmette-Guerin (320, 99%). Thirty-nine (12%) mothers were TST-positive; 102 (32%) were QFT-Plus-positive. Among HIV-exposed infants, 154 (95%) received antiretrovirals for HIV prevention and 141 (83%) of their mothers ever received isoniazid preventive therapy (IPT). Cumulative 24-month infant Mtb infection incidence was 3.6/100 person-years (PY) [95% confidence interval (CI): 2.4-5.5/100 PY]; 5.4/100 PY in HIV-exposed infants (10%, 17/170) versus 1.7/100 PY in HIV-unexposed infants (3.3%, 5/152) [hazard ratio (HR): 3.1 (95% CI: 1.2-8.5)]. More TST conversions occurred in the first versus second year of life [5.8 vs. 2.0/100 PY; HR: 2.9 (95% CI: 1.0-10.1)]. Infant TST-positivity was associated with maternal TST-positivity [HR: 2.9 (95% CI: 1.1-7.4)], but not QFT-Plus-positivity. Among HIV-exposed children, Mtb infection incidence was similar regardless of maternal IPT.
Mtb infection incidence (by TST) by 24 months of age was ~3-fold higher among HIV-exposed children, despite high maternal IPT uptake. Overall, more TST conversions occurred in the first 12 months compared to 12-24 months of age, similar in both HIV-exposed and HIV-unexposed children.
母婴 HIV 对婴儿结核分枝杆菌(Mtb)感染风险的影响尚不清楚。
在肯尼亚的一项纵向队列中招募了有/无 HIV 的孕妇及其婴儿。母亲在妊娠时进行干扰素 γ 释放试验(QFT-Plus)和结核菌素皮肤试验(TST);儿童在 12 和 24 个月时进行 TST。我们使用 Cox 比例风险回归估计婴儿 TST 阳性的发生率和相关因素。
在 322 名婴儿中,170 名(53%)有 HIV 暴露,152 名(47%)无 HIV 暴露。中位入组年龄为 6.6 周[四分位间距(IQR):6.1-10.0];大多数婴儿接受了卡介苗(320 名,99%)。39 名母亲 TST 阳性;102 名 QFT-Plus 阳性。在 HIV 暴露的婴儿中,154 名(95%)接受了抗逆转录病毒药物预防 HIV,141 名(83%)母亲接受了异烟肼预防治疗(IPT)。累积 24 个月婴儿 Mtb 感染发生率为 3.6/100 人年(95%置信区间[CI]:2.4-5.5/100 PY);HIV 暴露婴儿为 5.4/100 PY(10%,17/170),HIV 未暴露婴儿为 1.7/100 PY(3.3%,5/152)[风险比(HR):3.1(95% CI:1.2-8.5)]。第一年与第二年相比,TST 转换更多[5.8 比 2.0/100 PY;HR:2.9(95% CI:1.0-10.1)]。婴儿 TST 阳性与母亲 TST 阳性相关[HR:2.9(95% CI:1.1-7.4)],但与 QFT-Plus 阳性无关。在 HIV 暴露的儿童中,无论母亲是否接受 IPT,Mtb 感染的发生率相似。
尽管母亲 IPT 使用率很高,但 HIV 暴露儿童在 24 个月时的 Mtb 感染发生率(通过 TST 检测)仍高出约 3 倍。总体而言,与 12-24 个月相比,12 个月内 TST 转换更多,在 HIV 暴露和未暴露的儿童中均如此。