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HIV-1 Integrase Sequence Variability in Antiretroviral Naïve Patients and in Triple-Class Experienced Patients Subsequently Treated with Raltegravir

机译:HIV-1整合酶序列变异性在抗逆转录病毒初治患者和三级有经验的患者中随后接受拉格达韦治疗

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摘要

Viruses were sequenced from 75 antiretroviral therapy (ARV)-naïve and from 75 ARV-treated patients who subsequently received a raltegravir-containing regimen. No major integrase inhibitor (INI)-resistance mutations were present in the 150 integrase (IN) sequences. Four ARV-naïve (5.3%) and two ARV-treated patients (2.7%) had one of the following minor INI-resistance mutations: L74M, E157Q, G163R, and R263K but there was no association between baseline raltegravir genotype and subsequent response to raltegravir treatment. We also combined our sequences with 4170 previously published group M IN sequences from INI-naïve patients to assess IN sequence variability and compared our findings with those of a study we performed in 2008 using data from 1563 patients. The number of polymorphic IN positions increased from 40% to 41% between the two studies. However, none of the major INI-resistance mutations was found to be polymorphic in either study and there were no significant changes in the prevalence of any of the minor INI-resistance mutations.
机译:从75位未接受过抗逆转录病毒治疗(ARV)的病毒和75位接受抗逆转录病毒治疗的患者(随后接受含raltegravir的方案)中测序病毒。 150个整合酶(IN)序列中没有主要的整合酶抑制剂(INI)抗性突变。 4名初次接受ARV的患者(5.3%)和2例接受ARV的患者(2.7%)具有以下轻微的INI抵抗突变之一:L74M,E157Q,G163R和R263K,但基线拉格韦韦尔基因型与随后对raltegravir治疗。我们还将序列与来自INI初治患者的4170组先前发表的M IN序列进行了组合,以评估IN序列的变异性,并将我们的发现与2008年使用1563名患者的数据进行的研究相比较。在两项研究之间,多态IN位置的数量从40%增加到41%。但是,在任何一项研究中,没有发现主要的INI抵抗性突变是多态性的,任何次要的INI抵抗性突变的患病率也没有明显变化。

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