From the Centers for Disease Control and Prevention, Port-au-Prince, Haiti.
CARIS Foundation, Port-au-Prince, Haiti.
Pediatr Infect Dis J. 2019 May;38(5):503-507. doi: 10.1097/INF.0000000000002270.
The main objective of this study was to determine the frequency and patterns of HIV drug resistance-associated mutations among children under 18 months of age born to HIV-1-positive mothers enrolled in the prevention of mother-to-child transmission services in Haiti.
Between January 1, 2013 and December 31, 2014, HIV-positive remnant dried blood spots collected from children under 18 months of age for Early Infant Diagnosis at the National Public Health Laboratory were used for HIV-1 genotyping. HIV drug resistance mutations were analyzed using the Stanford Drug Resistance HIVdb program.
Of the 3555 dried blood spots collected for Early Infant Diagnosis, 360 (10.1%) were HIV-positive and 355 were available for genotyping. Of these, 304 (85.6%) were successfully genotyped and 217 (71.4%) had ≥1 drug resistance mutation. Mutations conferring resistance to nucleoside reverse transcriptase inhibitor (NRTIs) and non-NRTIs were present in 40.5% (123) and 69.1% (210), respectively. The most frequent mutations were K103N/S (48.0%), M184V (37.5%), G190A/S (15.1%), and Y181C/G/V (14.1%). Predicted drug resistance analysis revealed that 68.8% of the children had high-level resistance to non-NRTIs and 11.5% had intermediate to high-level resistance to abacavir.
This study showed high rates of resistance to NRTIs and non-NRTIs among newly HIV-diagnosed children in Haiti, suggesting that in the era of "Option B+" (initiation of lifelong combination antiretroviral therapy to pregnant women with HIV), the majority of children who acquire HIV infection through mother-to-child transmission of HIV have resistant HIV. These results have led the National HIV Program to revise the pediatric guidelines to include protease inhibitors in first-line regimens for all HIV-positive newborns.
本研究的主要目的是确定在海地参与母婴传播预防服务的 HIV-1 阳性母亲所生的 18 个月以下儿童中,与 HIV 耐药相关的突变的频率和模式。
2013 年 1 月 1 日至 2014 年 12 月 31 日,使用国家公共卫生实验室从 18 个月以下的早期婴儿诊断中收集的 HIV 阳性残余干血斑进行 HIV-1 基因分型。使用斯坦福药物耐药性 HIVdb 程序分析 HIV 耐药突变。
在为早期婴儿诊断收集的 3555 个干血斑中,有 360 个(10.1%)为 HIV 阳性,其中 355 个可用于基因分型。其中,304 个(85.6%)成功进行了基因分型,217 个(71.4%)有≥1 种耐药突变。核苷逆转录酶抑制剂(NRTIs)和非核苷逆转录酶抑制剂(NNRTIs)耐药相关的突变分别存在于 40.5%(123 个)和 69.1%(210 个)中。最常见的突变是 K103N/S(48.0%)、M184V(37.5%)、G190A/S(15.1%)和 Y181C/G/V(14.1%)。预测药物耐药性分析显示,68.8%的儿童对非 NRTIs 具有高水平耐药性,11.5%的儿童对阿巴卡韦具有中至高水平耐药性。
本研究表明,海地新诊断出的 HIV 儿童中存在高比例的 NRTIs 和 NNRTIs 耐药性,这表明在“B+选项”(对感染 HIV 的孕妇开始终生联合抗逆转录病毒治疗)时代,通过母婴传播感染 HIV 的大多数儿童都有耐药性 HIV。这些结果促使国家艾滋病毒规划修订儿科指南,将蛋白酶抑制剂纳入所有 HIV 阳性新生儿的一线治疗方案。