AIDS Immunopathogenesis Unit, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Crtra. Majadahonda Pozuelo Km2, 28220, Majadahonda, Madrid, Spain.
Expert Rev Anti Infect Ther. 2013 Dec;11(12):1291-302. doi: 10.1586/14787210.2013.852469. Epub 2013 Nov 6.
Assessment of HIV coreceptor tropism assay is recommended before starting therapy with CCR5 coreceptor antagonists. So far, only maraviroc (MVC) has been approved for clinical use and a tropism assay is mandatory for patients with virological failure or patients in which MVC is considered into future treatment options. Viral tropism can be assessed with either genotypic or phenotypic methods and to this aim different techniques have been developed. However, it is unclear which assay is more appropriate for routine testing. In fact, although phenotypic assays are considered the gold standard as they directly measure the viral tropism and current versions allow detection of a lower threshold of minor CXCR4-dependent variants, the genotypic assays present major practical advantages for their use in the clinical setting.
在开始使用 CCR5 核心受体拮抗剂治疗之前,建议进行 HIV 核心受体嗜性检测。到目前为止,只有马拉维若(MVC)被批准用于临床使用,对于病毒学失败的患者或未来考虑使用 MVC 作为治疗方案的患者,必须进行嗜性检测。可以使用基因型或表型方法评估病毒嗜性,为此已经开发了不同的技术。然而,哪种检测方法更适合常规检测尚不清楚。事实上,尽管表型检测被认为是金标准,因为它们可以直接测量病毒的嗜性,并且当前的版本可以检测到较低阈值的次要 CXCR4 依赖性变体,但基因型检测在临床环境中的使用具有重要的实际优势。