首页> 外文OA文献 >Performance of the VERSANT® HIV-1 Resistance Assays (LiPA) for detecting drug resistance in therapy-naive patients infected with different HIV-1 subtypes
【2h】

Performance of the VERSANT® HIV-1 Resistance Assays (LiPA) for detecting drug resistance in therapy-naive patients infected with different HIV-1 subtypes

机译:VERSANT®HIV-1耐药性检测方法(LiPA)在未接受过HIV-1亚型感染的初治患者中检测耐药性的性能

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

In this study we evaluated the performance of the VERSANT® HIV-1 Resistance Assays (LiPA) in detecting drug resistance in therapy-naive HIV-infected patients diagnosed in Belgium in 2000. We compared the results with population sequencing and found concordance to be in line with previous studies in treatment-experienced patients (86.87% for reverse transcriptase (RT); 92.77% for protease (PRO)). Discordance was mainly due to indeterminate reactions on LiPA (8.45% for RT; 6.85% for PRO) and minor discordances (4.13% for RT; 0.25% for PRO). Major discordances were rare (0.46% for RT; 0.12% for PRO). Indeterminate reactions were significantly associated with strains belonging to non-B subtypes. © 2003 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
机译:在这项研究中,我们评估了VERSANT®HIV-1耐药性分析(LiPA)在检测2000年在比利时诊断为未经治疗的HIV感染患者中检测耐药性的性能。我们将结果与人群测序进行了比较,发现一致性与先前有治疗经验的患者的研究一致(逆转录酶(RT)为86.87%;蛋白酶(PRO)为92.77%)。不一致主要是由于对LiPA的反应不确定(RT的为8.45%; PRO的为6.85%)和较小的不一致(RT的为4.13%; PRO的为0.25%)。重大矛盾很少见(RT为0.46%; PRO为0.12%)。不确定的反应与属于非B亚型的菌株显着相关。 ©2003欧洲微生物学会联合会。由Elsevier B.V.发布。保留所有权利。

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号