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在一项用于预防母婴传播的三联抗逆转录病毒预防的单臂试验中,感染 HIV 的母亲所生的母乳喂养婴儿中 HIV-1 耐药性的出现:一项二次分析。

HIV-1 drug resistance emergence among breastfeeding infants born to HIV-infected mothers during a single-arm trial of triple-antiretroviral prophylaxis for prevention of mother-to-child transmission: a secondary analysis.

机构信息

Division of HIV/AIDS Prevention, US Centers for Disease Control and Prevention, Kisumu, Kenya.

出版信息

PLoS Med. 2011 Mar;8(3):e1000430. doi: 10.1371/journal.pmed.1000430. Epub 2011 Mar 29.


DOI:10.1371/journal.pmed.1000430
PMID:21468304
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3066134/
Abstract

BACKGROUND: Nevirapine and lamivudine given to mothers are transmitted to infants via breastfeeding in quantities sufficient to have biologic effects on the virus; this may lead to an increased risk of a breastfed infant's development of resistance to maternal antiretrovirals. The Kisumu Breastfeeding Study (KiBS), a single-arm open-label prevention of mother-to-child HIV transmission (PMTCT) trial, assessed the safety and efficacy of zidovudine, lamivudine, and either nevirapine or nelfinavir given to HIV-infected women from 34 wk gestation through 6 mo of breastfeeding. Here, we present findings from a KiBS trial secondary analysis that evaluated the emergence of maternal ARV-associated resistance among 32 HIV-infected breastfed infants. METHODS AND FINDINGS: All infants in the cohort were tested for HIV infection using DNA PCR at multiple study visits during the 24 mo of the study, and plasma RNA viral load for all HIV-PCR-positive infants was evaluated retrospectively. Specimens from mothers and infants with viral load >1,000 copies/ml were tested for HIV drug resistance mutations. Overall, 32 infants were HIV infected by 24 mo of age, and of this group, 24 (75%) infants were HIV infected by 6 mo of age. Of the 24 infants infected by 6 mo, nine were born to mothers on a nelfinavir-based regimen, whereas the remaining 15 were born to mothers on a nevirapine-based regimen. All infants were also given single-dose nevirapine within 48 hours of birth. We detected genotypic resistance mutations in none of eight infants who were HIV-PCR positive by 2 wk of age (specimens from six infants were not amplifiable), for 30% (6/20) at 6 wk, 63% (14/22) positive at 14 wk, and 67% (16/24) at 6 mo post partum. Among the 16 infants with resistance mutations by 6 mo post partum, the common mutations were M184V and K103N, conferring resistance to lamivudine and nevirapine, respectively. Genotypic resistance was detected among 9/9 (100%) and 7/15 (47%) infected infants whose mothers were on nelfinavir and nevirapine, respectively. No mutations were detected among the eight infants infected after the breastfeeding period (age 6 mo). CONCLUSIONS: Emergence of HIV drug resistance mutations in HIV-infected infants occurred between 2 wk and 6 mo post partum, most likely because of exposure to maternal ARV drugs through breast milk. Our findings may impact the choice of regimen for ARV treatment of HIV-infected breastfeeding mothers and their infected infants.

摘要

背景:通过母乳喂养,替诺福韦和拉米夫定会从母亲传播给婴儿,其数量足以对病毒产生生物学效应;这可能会增加母乳喂养婴儿对母亲抗逆转录病毒药物产生耐药性的风险。基苏木母乳喂养研究(KiBS)是一项单臂开放性预防母婴 HIV 传播(PMTCT)试验,评估了从 34 孕周至母乳喂养 6 个月期间,替诺福韦、拉米夫定和奈韦拉平或奈非那韦用于 HIV 感染妇女的安全性和疗效。在这里,我们提出了 KiBS 试验二次分析的结果,该分析评估了 32 名 HIV 感染的母乳喂养婴儿中出现的与母亲 ARV 相关的耐药性。

方法和发现:在研究的 24 个月期间,所有队列中的婴儿都在多个研究访视中使用 DNA PCR 检测 HIV 感染情况,对所有 HIV-PCR 阳性婴儿的血浆 RNA 病毒载量进行回顾性评估。对病毒载量>1000 拷贝/ml 的母亲和婴儿的标本进行 HIV 耐药突变检测。总体而言,32 名婴儿在 24 个月时感染了 HIV,其中 24 名(75%)婴儿在 6 个月时感染了 HIV。在 24 名在 6 个月时感染的婴儿中,有 9 名婴儿的母亲使用奈非那韦为基础的方案,而其余 15 名婴儿的母亲使用奈韦拉平为基础的方案。所有婴儿在出生后 48 小时内还接受了单剂量奈韦拉平治疗。在 2 周龄时,有 8 名 HIV-PCR 阳性婴儿(6 名婴儿的标本不可扩增),6 周时 30%(6/20),14 周时 63%(22/22),产后 6 个月时 67%(24/24)检测到基因型耐药突变。在产后 6 个月时具有耐药突变的 16 名婴儿中,常见的突变是 M184V 和 K103N,分别导致对拉米夫定和奈韦拉平的耐药性。在分别使用奈非那韦和奈韦拉平的母亲的 9/9(100%)和 7/15(47%)感染婴儿中检测到基因型耐药。在母乳喂养期(6 月龄)后感染的 8 名婴儿中未检测到突变。

结论:HIV 感染婴儿的 HIV 耐药突变出现在产后 2 周至 6 个月之间,最有可能是因为通过母乳接触了母亲的 ARV 药物。我们的发现可能会影响 ARV 治疗 HIV 感染的母乳喂养母亲及其感染婴儿的方案选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e91/3066134/cfcc9bad35ea/pmed.1000430.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e91/3066134/7f2dfdf10c47/pmed.1000430.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e91/3066134/cfcc9bad35ea/pmed.1000430.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e91/3066134/7f2dfdf10c47/pmed.1000430.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e91/3066134/cfcc9bad35ea/pmed.1000430.g002.jpg

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