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对于乌干达那些在围产期接受单剂量奈韦拉平治疗的婴儿,子宫内的HIV感染与奈韦拉平耐药风险增加有关。

In utero HIV infection is associated with an increased risk of nevirapine resistance in ugandan infants who were exposed to perinatal single dose nevirapine.

作者信息

Church Jessica D, Mwatha Anthony, Bagenda Danstan, Omer Saad B, Donnell Deborah, Musoke Philippa, Nakabiito Clemensia, Eure Chineta, Bakaki Paul, Matovu Flavia, Thigpen Michael C, Guay Laura A, McConnell Michelle, Fowler Mary Glenn, Jackson J Brooks, Eshleman Susan H

机构信息

Johns Hopkins University School of Medicine , Baltimore, Maryland 21205, USA.

出版信息

AIDS Res Hum Retroviruses. 2009 Jul;25(7):673-7. doi: 10.1089/aid.2009.0003.

Abstract

Use of single dose nevirapine (sdNVP) to prevent HIV mother-to-child transmission is associated with the emergence of NVP resistance in many infants who are HIV infected despite prophylaxis. We combined results from four clinical trials to analyze predictors of NVP resistance in sdNVP-exposed Ugandan infants. Samples were tested with the ViroSeq HIV Genotyping System and a sensitive point mutation assay (LigAmp, for detection of K103N, Y181C, and G190A). NVP resistance was detected at 6-8 weeks in 36 (45.0%) of 80 infants using ViroSeq and 33 (45.8%) of 72 infants using LigAmp. NVP resistance was more frequent among infants who were infected in utero than among infants who were diagnosed with HIV infection after birth by 6-8 weeks of age. Detection of NVP resistance at 6-8 weeks was not associated with HIV subtype (A vs. D), pre-NVP maternal viral load or CD4 cell count, infant viral load at 6-8 weeks, or infant sex. NVP resistance was still detected in some infants 6-12 months after sdNVP exposure. In this study, in utero HIV infection was the only factor associated with detection of NVP resistance in infants 6-8 weeks after sdNVP exposure.

摘要

使用单剂量奈韦拉平(sdNVP)预防艾滋病毒母婴传播与许多接受预防治疗但仍感染艾滋病毒的婴儿出现奈韦拉平耐药性有关。我们综合了四项临床试验的结果,以分析接触sdNVP的乌干达婴儿中奈韦拉平耐药性的预测因素。样本采用ViroSeq艾滋病毒基因分型系统和一种敏感的点突变检测方法(LigAmp,用于检测K103N、Y181C和G190A)进行检测。使用ViroSeq在80名婴儿中的36名(45.0%)以及使用LigAmp在72名婴儿中的33名(45.8%)在6 - 8周时检测到奈韦拉平耐药性。宫内感染的婴儿中奈韦拉平耐药性比出生后6 - 8周被诊断为艾滋病毒感染的婴儿更常见。在6 - 8周时检测到奈韦拉平耐药性与艾滋病毒亚型(A与D)、奈韦拉平治疗前母亲的病毒载量或CD4细胞计数以及婴儿在6 - 8周时的病毒载量或婴儿性别无关。在接触sdNVP后6 - 12个月,仍在一些婴儿中检测到奈韦拉平耐药性。在本研究中,宫内艾滋病毒感染是与sdNVP暴露后6 - 8周婴儿中检测到奈韦拉平耐药性相关的唯一因素。

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