临床环境中HIV-1嗜性的基因型测定

HIV therapy Pub Date : 2010-05-04 DOI:10.2217/HIV.10.15
L. C. Swenson, R. Boehme, A. Thielen, R. McGovern, P. Harrigan
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引用次数: 4

摘要

HIV通过CD4受体和一种辅助受体(通常是CCR5或CXCR4)进入细胞。病人的病毒所使用的特定的辅助受体被称为其趋向性。在使用CCR5拮抗剂治疗之前,有必要进行趋向性检测,以排除使用cxcr4的(X4)病毒的存在,表型Trofile™检测是HIV辅助受体使用的最常用检测。基因型趋向性检测相对于表型趋向性检测和性状分析具有一定的实际优势。基因型趋向性分析通常基于对HIV环境的V3环进行测序,并使用生物信息学算法进行分析,以推断病毒可能的辅助受体使用情况。基因型方法经过多年的完善和改进,最近被用作CCR5拮抗剂治疗的回顾性(偶尔也是前瞻性)筛选工具,如马拉维洛克。基因型趋向性检测的替代方法包括异双工跟踪测定,“深度”V3测序和c…
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genotypic determination of HIV-1 tropism in the clinical setting
HIV enters cells via the CD4 receptor and a coreceptor, generally CCR5 or CXCR4. The specific coreceptor used by a patient’s virus is referred to as its tropism. Tropism testing is necessary prior to treatment with CCR5 antagonist medication to rule out the presence of CXCR4-using (X4) virus, with the phenotypic Trofile™ assay being the most commonly used test for HIV coreceptor usage. Genotypic tropism testing may offer some practical advantages to phenotypic tropism testing and Trofile. Genotypic tropism assays are typically based on sequencing the V3 loop of HIV env and analysis using bioinformatic algorithms to infer the likely coreceptor usage of the virus. Genotypic methods have been refined and improved over the years and have recently been used as retrospective (and occasionally prospective) screening tools for treatment with CCR5 antagonist medication, such as maraviroc. Alternative approaches to genotypic tropism testing include heteroduplex tracking assays, ‘deep’ V3 sequencing and testing of c...
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