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首页> 外文期刊>Journal of Clinical Microbiology >Polymorphism of the Human Immunodeficiency Virus Type 1 (HIV-1) Protease Gene and Response of HIV-1-Infected Patients to a Protease Inhibitor
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Polymorphism of the Human Immunodeficiency Virus Type 1 (HIV-1) Protease Gene and Response of HIV-1-Infected Patients to a Protease Inhibitor

机译:人类免疫缺陷病毒1型(HIV-1)蛋白酶基因的多态性和HIV-1感染患者对蛋白酶抑制剂的反应。

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In order to analyze the impact of protease gene polymorphism on response to regimens containing a protease inhibitor, the entire protease coding domain from 58 human immunodeficiency virus type 1 (HIV-1)-infected patients who were protease inhibitor naive was sequenced before therapy was started. Plasma HIV-1 RNA levels were measured at baseline and at month 3 and month 6 after treatment. All patients were treated with a combination of two reverse transcriptase inhibitors and a protease inhibitor (saquinavir EOF [n = 28], ritonavir [n = 16], or indinavir [n = 14]). Before treatment, 30 different positions whose codons differed from the subtype B consensus sequence were observed. Major mutations associated with protease inhibitor resistance were not observed. No statistical correlation between the number of amino acid differences and the treatment efficacy at month 3 (?2.4 log) or month 6 (?2.7 log) was observed. At baseline, genotypic analysis of the HIV-1 protease gene of patients who have never received a protease inhibitor does not allow prediction of the efficacy of regimens containing a protease inhibitor.
机译:为了分析蛋白酶基因多态性对含有蛋白酶抑制剂的治疗方案反应的影响,在开始治疗之前对来自58名人类免疫缺陷病毒1型(HIV-1)感染的蛋白酶抑制剂天真的患者的整个蛋白酶编码域进行了测序。 。在基线以及治疗后第3个月和第6个月测量血浆HIV-1 RNA水平。所有患者均接受了两种逆转录酶抑制剂和蛋白酶抑制剂(沙奎那韦EOF [ n = 28],利托那韦[ n = 16]或茚地那韦[< em> n = 14])。在治疗之前,观察到30个密码子不同于B亚型共有序列的不同位置。没有观察到与蛋白酶抑制剂抗性相关的主要突变。在第3个月(≤2.4log)或第6个月(≤2.7log)时,未观察到氨基酸差异数量与治疗功效之间的统计相关性。在基线时,从未接受过蛋白酶抑制剂的患者的HIV-1蛋白酶基因的基因型分析无法预测含有蛋白酶抑制剂的治疗方案的疗效。

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