Bishop Marley D, Korutaro Violet, Boyce Ceejay L, Beck Ingrid A, Styrchak Sheila M, Knowles Kevin, Ziemba Lauren, Brummel Sean S, Coletti Anne, Jean-Philippe Patrick, Chakhtoura Nahida, Vhembo Tichaona, Cassim Haseena, Owor Maxensia, Fairlie Lee, Moyo Sikhulile, Chinula Lameck, Lockman Shahin, Frenkel Lisa M
Department of Global Infectious Diseases, Seattle Children's Research Institute, 307 Westlake Ave N, Seattle, 98109, Washington, USA.
Children's Foundation Uganda, Baylor College of Medicine, Block 5 Mulago Hospital, P. O. BOX 72052, Kampala 72052, Kamutarpala Uganda.
J Acquir Immune Defic Syndr. 2024 Aug;96(4):385-392. doi: 10.1097/qai.0000000000003435.
VESTED (NCT03048422) compared the safety and efficacy of three antiretroviral treatment () regimens in pregnant and postpartum women: dolutegravir+emtricitabine/tenofovir alafenamide fumarate; dolutegravir+emtricitabine/tenofovir disoproxil fumarate (); efavirenz/emtricitabine/TDF. Vertical HIV transmission () occurred to 4/617 (0.60%) live-born infants, who were evaluated for HIV drug resistance () and other risk factors.
In 2018-2020, pregnant (weeks-14-28) women living with HIV and ≤14 days of ART were enrolled at 22 international sites and followed with their infants through 50 weeks postpartum.
HIV sequences derived by single genome amplification () from longitudinally collected specimens were assessed from VT Cases for HIVDR in protease, reverse transcriptase, integrase, and the 3'polypurine tract ().
The four Case mothers were prescribed efavirenz-based-ART for 1-7 days prior to randomization to study ART. Their infants received postnatal nevirapine+/-zidovudine prophylaxis and were breastfed. A total of 833 SGA sequences were derived. The "major" (Stanford HIVDR Score ≥60) non-nucleoside reverse transcriptase inhibitor () mutation (K103N) was detected persistently in one viremic mother, and likely contributed to VT of HIVDR. Major NNRTI HIVDR mutations were detected in all three surviving infants. No integrase, nor high frequencies of 3'PPT mutations conferring dolutegravir HIVDR were detected. The timing of HIV infant diagnosis, plasma HIV RNA levels and HIVDR suggests one , one peripartum, one early, and one late breastfeeding transmission.
VT was rare. New-onset NNRTI HIVDR in Case mothers was likely from efavirenz-ART prescribed prior to study dolutegravir-ART, and in one case appeared transmitted to the infant despite nevirapine prophylaxis.
VESTED(NCT03048422)比较了三种抗逆转录病毒治疗(ART)方案在孕妇和产后妇女中的安全性和有效性:多替拉韦+恩曲他滨/替诺福韦艾拉酚胺富马酸盐;多替拉韦+恩曲他滨/替诺福韦酯(TDF);依非韦伦/恩曲他滨/替诺福韦(TDF)。617名活产婴儿中有4名(0.60%)发生了垂直HIV传播(VPT),对这些婴儿进行了HIV耐药性(HIVDR)及其他风险因素评估。
2018年至2020年,HIV感染孕妇(孕周14 - 28周)且接受抗逆转录病毒治疗(ART)≤14天,在22个国际研究点入组,并对其婴儿随访至产后50周。
通过单基因组扩增(SGA)从纵向采集的标本中获得HIV序列,对VPT病例的蛋白酶、逆转录酶、整合酶及3'多聚嘌呤区(3'PPT)进行HIV耐药性(HIVDR)评估。
4例病例的母亲在随机分组接受研究性ART治疗前1 - 7天接受基于依非韦伦的ART治疗。她们的婴儿接受了产后奈韦拉平+/-齐多夫定预防治疗并进行母乳喂养。共获得833条SGA序列。在1例病毒血症母亲中持续检测到“主要”(斯坦福HIVDR评分≥60)非核苷类逆转录酶抑制剂(NNRTI)突变(K103N),这可能导致了HIVDR的VPT。在所有3名存活婴儿中均检测到主要的NNRTI HIVDR突变。未检测到整合酶突变,也未检测到导致多替拉韦HIVDR的高频率3'PPT突变。HIV婴儿诊断时间、血浆HIV RNA水平及HIVDR提示1例为宫内感染,1例为围产期感染,1例为早期感染,1例为晚期母乳喂养感染。
VPT罕见。病例母亲中新发的NNRTI HIVDR可能源于在研究性多替拉韦ART治疗前使用的依非韦伦ART治疗,且在1例病例中,尽管婴儿接受了奈韦拉平预防治疗,但仍出现了母婴传播。