Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
Clin Infect Dis. 2011 Apr 15;52(8):1069-76. doi: 10.1093/cid/cir008.
The World Health Organization currently recommends initiation of highly active antiretroviral therapy (HAART) for human immunodeficiency virus (HIV)-infected lactating women with CD4+ cell counts <350 cells/μL or stage 3 or 4 disease. We analyzed antiretroviral drug resistance in HIV-infected infants in the Post Exposure Prophylaxis of Infants trial whose mothers initiated HAART postpartum (with a regimen of nevirapine [NVP], stavudine, and lamivudine). Infants in the trial received single-dose NVP and a week of zidovudine (ZDV) at birth; some infants also received extended daily NVP prophylaxis, with or without extended ZDV prophylaxis.
We analyzed drug resistance in plasma samples collected from all HIV-infected infants whose mothers started HAART in the first postpartum year. Resistance testing was performed using the first plasma sample collected within 6 months after maternal HAART initiation. Categorical variables were compared by exact or trend tests; continuous variables were compared using rank-sum tests.
Multiclass resistance (MCR) was detected in HIV from 11 (29.7%) of 37 infants. Infants were more likely to develop MCR infection if their mothers initiated HAART earlier in the postpartum period (by 14 weeks vs after 14 weeks and up to 6 months vs after 6 months, P = .0009), or if the mother was exclusively breastfeeding at the time of HAART initiation (exclusive breastfeeding vs mixed feeding vs no breastfeeding, P = .003).
Postpartum maternal HAART initiation was associated with acquisition of MCR in HIV-infected breastfeeding infants. The risk was higher among infants whose mothers initiated HAART closer to the time of delivery or were still exclusively breastfeeding when they first reported HAART use.
世界卫生组织目前建议对 CD4+ 细胞计数<350 个/μL 或处于 3 或 4 期疾病的感染人类免疫缺陷病毒(HIV)的哺乳期妇女启动高效抗逆转录病毒治疗(HAART)。我们分析了在母婴 HIV 暴露后预防试验(Post Exposure Prophylaxis of Infants trial)中接受 HAART 产后治疗(采用奈韦拉平[NVP]、司他夫定和拉米夫定方案)的 HIV 感染婴儿的抗逆转录病毒药物耐药情况。试验中的婴儿在出生时接受了单剂量 NVP 和一周的齐多夫定(ZDV);一些婴儿还接受了扩展的每日 NVP 预防,无论是否同时接受了扩展的 ZDV 预防。
我们分析了在母亲产后第一年开始接受 HAART 的所有 HIV 感染婴儿的血浆样本中药物耐药情况。耐药性检测是使用在母亲开始 HAART 后 6 个月内采集的第一份血浆样本进行的。分类变量通过确切或趋势检验进行比较;连续变量通过秩和检验进行比较。
37 例婴儿中有 11 例(29.7%)的 HIV 存在多重耐药(MCR)。如果母亲在产后更早(14 周内 vs 14 周后至 6 个月内 vs 6 个月后)开始 HAART,或者在开始 HAART 时母亲仍在进行纯母乳喂养(纯母乳喂养 vs 混合喂养 vs 非母乳喂养),婴儿更有可能发生 MCR 感染(P =.0009)。
产后母亲 HAART 启动与 HIV 感染母乳喂养婴儿获得 MCR 相关。在母亲分娩时或首次报告 HAART 使用时仍在进行纯母乳喂养的婴儿中,这种风险更高。