Transplantation and Clinical Virology, Department of Biomedicine, University of Basel, Switzerland.
Transplantation and Clinical Virology, Department of Biomedicine, University of Basel, Switzerland / Clinical Virology, Laboratory Medicine, University Hospital Basel, Switzerland.
Swiss Med Wkly. 2019 Apr 4;149:w20059. doi: 10.4414/smw.2019.20059. eCollection 2019 Mar 25.
Combination antiretroviral therapy (cART) has reduced mother-to-child transmissions (MTCT) and improved the prognosis of HIV-infected newborns. However, drug resistance mutations (DRM) in HIV-infected children, either transmitted by MTCT (HIV-tDRM) or selected by suboptimal adherence and drug levels (HIV-sDRM), remain a concern. We sought to determine the rate of HIV-tDRM and HIV-sDRM in MTCT pairs in Switzerland.
We performed a retrospective analysis of prospectively collected clinical data and available stored samples from MTCT pairs participating in the Swiss Mother-Child HIV (MoCHIV) cohort.
We identified 22 HIV-infected mother-child pairs with delivery between 1989 and 2009 who had 15 years of follow-up (33% white ethnicity). Twenty-one women (96%) were treatment-naïve before pregnancy, 8 (36%) had an unknown HIV status and delivered vaginally, 2 were diagnosed but not treated, and 11 (50%) received antiretrovirals during pregnancy or at delivery, of whom only 6 cases (27%) had cART. HIV subtypes were concordant in all mother-child pairs (subtype B 13/22 [59%]). Using stored plasma (n = 66) and mononuclear cell (n = 43) samples from the children, HIV-tDRM (M184V) was identified in 1 of 22 (4.5%) mothers (1/11 treated, 9%) and was followed by HIV-sDRM at 10 months of age. HIV-sDRM (M184V 23%; K103N 4.5%; D67N 13.6%) occurred in 16/22 (73%) after 4 years, half of whom were treatment naïve. HIV-sDRM were associated with a lower CD4 T-cell nadir (p <0.05) and tended to have higher viral loads and more frequent cART changes.
HIV-tDRM were low in this Swiss MoCHIV cohort, making them a minor yet preventable complication of prenatal HIV care, whereas HIV-sDRM are a significant challenge in paediatric HIV care.
联合抗逆转录病毒疗法(cART)降低了母婴传播(MTCT)的风险,并改善了 HIV 感染新生儿的预后。然而,HIV 感染儿童中存在的耐药突变(DRM),无论是通过 MTCT 传播(HIV-tDRM)还是由于不适当的依从性和药物水平选择(HIV-sDRM)而产生的,仍然令人担忧。我们旨在确定瑞士 MTCT 对中 HIV-tDRM 和 HIV-sDRM 的发生率。
我们对参与瑞士母婴 HIV(MoCHIV)队列的前瞻性收集的临床数据和可用的存储样本进行了回顾性分析。
我们确定了 22 例在 1989 年至 2009 年期间分娩的 HIV 感染母婴对,这些母婴对有 15 年的随访(33%为白种人)。21 名妇女(96%)在怀孕前未接受过治疗,8 名(36%)阴道分娩时 HIV 状态未知,2 名被诊断但未治疗,11 名(50%)在怀孕期间或分娩时接受了抗逆转录病毒治疗,其中只有 6 例(27%)接受了 cART。所有母婴对的 HIV 亚型均一致(亚型 B 13/22 [59%])。使用儿童的储存血浆(n=66)和单核细胞(n=43)样本,在 22 名母亲中的 1 名(11 名治疗者中的 1 名,9%)中发现了 HIV-tDRM(M184V),并在 10 个月龄时出现了 HIV-sDRM。在 4 年后,16/22(73%)名儿童出现了 HIV-sDRM(M184V 23%;K103N 4.5%;D67N 13.6%),其中一半为未经治疗的儿童。HIV-sDRM 与 CD4 T 细胞最低点较低(p <0.05)相关,且病毒载量较高,更频繁地进行 cART 改变。
在瑞士 MoCHIV 队列中,HIV-tDRM 较低,这是产前 HIV 护理中可预防的小并发症,而 HIV-sDRM 是儿科 HIV 护理中的重大挑战。