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在对拉替拉韦耐药性降低的临床标本中,雅培实时 HIV-1 病毒载量检测所针对的 HIV-1 整合酶区域的序列变异最小。

Minimal sequence variability of the region of HIV-1 integrase targeted by the Abbott RealTime HIV-1 viral load assay in clinical specimens with reduced susceptibility to raltegravir.

机构信息

Abbott Molecular, Des Plaines, IL USA; University of California San Francisco, Department of Community Health, San Francisco, CA, USA.

出版信息

J Virol Methods. 2013 Nov;193(2):693-6. doi: 10.1016/j.jviromet.2013.07.028. Epub 2013 Jul 25.

DOI:10.1016/j.jviromet.2013.07.028
PMID:23892128
Abstract

The Abbott RealTime (ART) HIV-1 assay targets the integrase region and is designed to tolerate mismatches. Variability in integrase sequences comprising the assay target regions from >1000 clinical specimens submitted for phenotypic and genotypic raltegravir resistance testing were analyzed. In this large collection of sequences from clinical specimens, the number and location of raltegravir resistance associated mutations did not differ from those tested previously and shown not to result in under-estimation of viral loads.

摘要

雅培实时(ART)HIV-1 检测法针对整合酶区域,旨在容忍错配。对提交进行表型和基因型拉替拉韦耐药性检测的 >1000 个临床标本中,检测目标区域的整合酶序列的变异性进行了分析。在该临床标本的大型序列集中,拉替拉韦耐药相关突变的数量和位置与之前测试的结果一致,且不会导致病毒载量的低估。

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Minimal sequence variability of the region of HIV-1 integrase targeted by the Abbott RealTime HIV-1 viral load assay in clinical specimens with reduced susceptibility to raltegravir.在对拉替拉韦耐药性降低的临床标本中,雅培实时 HIV-1 病毒载量检测所针对的 HIV-1 整合酶区域的序列变异最小。
J Virol Methods. 2013 Nov;193(2):693-6. doi: 10.1016/j.jviromet.2013.07.028. Epub 2013 Jul 25.
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Performance of the Abbott RealTime HIV-1 viral load assay is not impacted by integrase inhibitor resistance-associated mutations.Abbott RealTime HIV-1 病毒载量测定法的性能不受整合酶抑制剂耐药相关突变的影响。
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Evolution patterns of raltegravir-resistant mutations after integrase inhibitor interruption.整合酶抑制剂中断治疗后拉替拉韦耐药突变的进化模式。
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Genotypic/phenotypic patterns of HIV-1 integrase resistance to raltegravir.HIV-1 整合酶对拉替拉韦耐药的基因/表型模式。
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The HIV-1 integrase G118R mutation confers raltegravir resistance to the CRF02_AG HIV-1 subtype.HIV-1 整合酶 G118R 突变使 CRF02_AG 型 HIV-1 对拉替拉韦产生耐药性。
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Mutation N155H in HIV-2 integrase confers high phenotypic resistance to raltegravir and impairs replication capacity.HIV-2整合酶中的N155H突变赋予对raltegravir的高表型耐药性并损害复制能力。
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The HIV-1 integrase genotype strongly predicts raltegravir susceptibility but not viral fitness of primary virus isolates.HIV-1 整合酶基因型强烈预测拉替拉韦的敏感性,但不能预测原发性病毒分离物的病毒适应性。
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No residual activity of raltegravir after development of 148 complex mutations in vivo.在体内出现148种复合突变后,拉替拉韦无残留活性。
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Primary mutations selected in vitro with raltegravir confer large fold changes in susceptibility to first-generation integrase inhibitors, but minor fold changes to inhibitors with second-generation resistance profiles.体外使用拉替拉韦选择的原发性突变可导致对第一代整合酶抑制剂的敏感性发生大幅度变化,但对具有第二代耐药谱的抑制剂仅有较小的变化倍数。
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HIV-1 integrase variability and relationship with drug resistance in antiretroviral-naive and -experienced patients with different HIV-1 subtypes.不同HIV-1亚型的初治和经治患者中HIV-1整合酶的变异性及其与耐药性的关系
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