首页> 外文期刊>The Pediatric infectious disease journal >Lopinavir/ritonavir-based antiretroviral therapy in human immunodeficiency virus type 1-infected naive children: rare protease inhibitor resistance mutations but high lamivudine/emtricitabine resistance at the time of virologic failure.
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Lopinavir/ritonavir-based antiretroviral therapy in human immunodeficiency virus type 1-infected naive children: rare protease inhibitor resistance mutations but high lamivudine/emtricitabine resistance at the time of virologic failure.

机译:基于罗匹那韦/利托那韦的抗逆转录病毒疗法在人类免疫缺陷病毒1型感染的纯净儿童中的应用:罕见的蛋白酶抑制剂耐药性突变,但在病毒学失败时对拉米夫定/恩曲他滨耐药性较高。

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BACKGROUND: Lopinavir/ritonavir (LPV/r) is now the protease inhibitor regimen of choice in the first-line antiretroviral therapy for children <6 years of age. METHODS: We included all the human immunodeficiency virus (HIV) type 1-infected highly active antiretroviral therapy (HAART)-naive children who started an LPV/r-based regimen between 2000 and 2009 at the Necker Hospital (Paris, France). Virologic failure (VF) was defined as an HIV-RNA >/=50 copies/mL. Resistance genotypic test was performed in case of VF. RESULTS: A total of 43 children were included at a median age of 4.8 years (1.8-8.0). Median level of HIV RNA and percentage of CD4 cell count was 5.5 log copies/mL (4.6-6) and 15% (8-27.5), respectively. HAART included LPV/r and 2 nucleoside reverse-transcriptase inhibitors, mainly lamivudine (3TC), zidovudine, and/or abacavir. The median follow-up period was 36 months (18-72). Less than 50 copies/mL of HIV RNA was observed in 46%, 67%, and 70% of the children at months 6, 9, and 12, respectively. In all, 20 children (46.5%) experienced a VF. The risk factors of primary VF were a young age and a low socioeconomic status. The genotypic resistance test, performed for 18 of 20 children with VF, revealed 1 LPV/r-resistant virus and protease inhibitor-related major mutations without LPV/r resistance in 2 other children. Of the 18 children with VF, 15 received a 3TC-based HAART: 12 of 15 (80%) harbored a 3TC-resistant virus. No virus resistant to zidovudine or abacavir was found. CONCLUSION: In all, 70% of HAART-naive children had virologic success at month 12. The selection of LPV-resistant strains was a rare event. A high rate of selection of 3TC-mutations strengthens the recommendation to prefer a first-line 3TC-sparing regimen, particularly for children with risk factors of poor adherence.
机译:背景:洛匹那韦/利托那韦(LPV / r)现在是针对6岁以下儿童的一线抗逆转录病毒疗法中首选的蛋白酶抑制剂方案。方法:我们纳入了所有感染了1型人类免疫缺陷病毒(HIV)的未曾接受过治疗的幼稚儿童,这些儿童在2000年至2009年之间在法国内克医院(法国巴黎)开始了基于LPV / r的治疗方案。病毒学衰竭(VF)定义为HIV-RNA> / = 50拷贝/ mL。在发生VF的情况下进行了耐药基因型测试。结果:总共包括43名儿童,中位年龄为4.8岁(1.8-8.0)。 HIV RNA的中位水平和CD4细胞计数的百分比分别为5.5 log拷贝/ mL(4.6-6)和15%(8-27.5)。 HAART包括LPV / r和2种核苷逆转录酶抑制剂,主要是拉米夫定(3TC),齐多夫定和/或阿巴卡韦。中位随访期为36个月(18-72)。在第6、9和12个月时,分别有46%,67%和70%的儿童观察到不足50拷贝/ mL的HIV RNA。共有20名儿童(46.5%)经历了室颤。原发性室颤的危险因素是年轻和低社会经济地位。对20名VF儿童中的18名进行了基因型耐药性测试,发现另外2名儿童中有1种LPV / r耐药性病毒和蛋白酶抑制剂相关的主要突变,而没有LPV / r耐药性。在18名VF儿童中,有15名接受了基于3TC的HAART:15名儿童中有12名(80%)携带了3TC抗药性病毒。未发现对齐多夫定或阿巴卡韦有抗药性的病毒。结论总共有70%的未接受HAART的儿童在第12个月获得病毒学成功。选择LPV耐药菌株是罕见的事件。对3TC突变的选择率很高,进一步推荐了首选一线保留3TC的方案,特别是对于依从性差的危险因素的儿童。

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