Yek Christina, Massanella Marta, Peling Tashi, Lednovich Kristen, Nair Sangeetha V, Worlock Andrew, Vargas Milenka, Gianella Sara, Ellis Ronald J, Strain Matthew C, Busch Michael P, Nugent C Thomas, Richman Douglas D
University of California San Diego, La Jolla, California, USA.
Hologic Incorporated, San Diego, California, USA.
J Clin Microbiol. 2017 Aug;55(8):2544-2553. doi: 10.1128/JCM.00425-17. Epub 2017 Jun 7.
The search for a cure for HIV infection has highlighted the need for increasingly sensitive and precise assays to measure viral burden in various tissues and body fluids. We describe the application of a standardized assay for HIV-1 RNA in multiple specimen types. The fully automated Aptima HIV-1 Quant Dx assay (Aptima assay) is FDA cleared for blood plasma HIV-1 RNA quantitation. In this study, the Aptima assay was applied for the quantitation of HIV RNA in peripheral blood mononuclear cells (PBMCs; = 72), seminal plasma ( = 20), cerebrospinal fluid (CSF; = 36), dried blood spots (DBS; = 104), and dried plasma spots (DPS; = 104). The Aptima assay was equivalent to or better than commercial assays or validated in-house assays for the quantitation of HIV RNA in CSF and seminal plasma. For PBMC specimens, the sensitivity of the Aptima assay in the detection of HIV RNA decayed as background uninfected PBMC counts increased; proteinase K treatment demonstrated some benefit in restoring signal at higher levels of background PBMCs. Finally, the Aptima assay yielded 100% detection rates of DBS in participants with plasma HIV RNA levels of ≥35 copies/ml and 100% detection rates of DPS in participants with plasma HIV RNA levels of ≥394 copies/ml. The Aptima assay can be applied to a variety of specimens from HIV-infected subjects to measure HIV RNA for studies of viral persistence and cure strategies. It can also detect HIV in dried blood and plasma specimens, which may be of benefit in resource-limited settings.
寻找治愈HIV感染的方法凸显了对越来越灵敏和精确的检测方法的需求,以测量各种组织和体液中的病毒载量。我们描述了一种针对多种标本类型的HIV-1 RNA标准化检测方法的应用。全自动Aptima HIV-1定量Dx检测法(Aptima检测法)已获得美国食品药品监督管理局(FDA)批准,用于血浆中HIV-1 RNA定量。在本研究中,Aptima检测法被应用于外周血单个核细胞(PBMC;n = 72)、精液血浆(n = 20)、脑脊液(CSF;n = 36)、干血斑(DBS;n = 104)和干血浆斑(DPS;n = 104)中HIV RNA的定量。对于CSF和精液血浆中HIV RNA的定量,Aptima检测法等同于或优于商业检测法或经过验证的内部检测法。对于PBMC标本,随着未感染PBMC背景计数的增加,Aptima检测法检测HIV RNA的灵敏度下降;蛋白酶K处理在恢复较高背景PBMC水平下的信号方面显示出一定益处。最后,对于血浆HIV RNA水平≥35拷贝/ml的参与者,Aptima检测法对DBS的检测率为100%,对于血浆HIV RNA水平≥394拷贝/ml的参与者,对DPS的检测率为100%。Aptima检测法可应用于HIV感染受试者的多种标本,以测量HIV RNA,用于病毒持续性和治愈策略的研究。它还可以检测干血和血浆标本中的HIV,这在资源有限的环境中可能有益。