Maternal Human Immunodeficiency Virus (HIV) Drug Resistance Is Associated With Vertical Transmission and Is Prevalent in Infected Infants

母乳喂养 医学 奈韦拉平 传输(电信) 病毒载量 抗药性 母乳喂养 艾滋病毒耐药性 怀孕 免疫学 儿科 病毒学 病毒 抗逆转录病毒疗法 生物 工程类 电气工程 微生物学 遗传学
作者
Ceejay L Boyce,Tatiana Sils,Daisy Ko,Annie Wong-On-Wing,Ingrid Beck,Sheila Styrchak,Patricia DeMarrais,Camlin Tierney,Lynda Stranix‐Chibanda,Patricia M. Flynn,Taha E. Taha,Maxensia Owor,Mary Glenn Fowler,Lisa M. Frenkel,Impaact Bf Promoting Maternal,Infant Survival Everywhere Study Team
出处
期刊:Clinical Infectious Diseases [Oxford University Press]
卷期号:74 (11): 2001-2009 被引量:6
标识
DOI:10.1093/cid/ciab744
摘要

Abstract Background We aimed to assess if maternal human immunodeficiency virus (HIV) drug resistance is associated with an increased risk of HIV vertical transmission and to describe the dynamics of drug resistance in HIV-infected infants. Methods This was a case-control study of PROMISE study participants. “Cases” were mother-infant pairs with HIV vertical transmission during pregnancy or breastfeeding and “controls” were mother-infant pairs without transmission matched 1:3 by delivery date and clinical site. Genotypic HIV drug resistance analyses were performed on mothers’ and their infants’ plasma at or near the time of infant HIV diagnosis. Longitudinal analysis of genotypic resistance was assessed in available specimens from infants, from diagnosis and beyond, including antiretroviral therapy (ART) initiation and last study visits. Results Our analyses included 85 cases and 255 matched controls. Maternal HIV drug resistance, adjusted for plasma HIV RNA load at infant HIV diagnosis, enrollment CD4 count, and antepartum regimens, was not associated with in utero/peripartum HIV transmission. In contrast, both maternal plasma HIV RNA load and HIV drug resistance were independent risk factors associated with vertical transmission during breastfeeding. Furthermore, HIV drug resistance was selected across infected infants during infancy. Conclusions Maternal HIV drug resistance and maternal viral load were independent risk factors for vertical transmission during breastfeeding, suggesting that nevirapine alone may be insufficient infant prophylaxis against drug-resistant variants in maternal breast milk. These findings support efforts to achieve suppression of HIV replication during pregnancy and suggest that breastfeeding infants may benefit from prophylaxis with a greater barrier to drug resistance than nevirapine alone.

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