Laboratory of Experimental Virology, Department of Medical Microbiology, and.
Department of Internal Medicine, Amsterdam UMC, University of Amsterdam, Amsterdam, Netherlands.
JCI Insight. 2020 Mar 26;5(6):134196. doi: 10.1172/jci.insight.134196.
Plasma viral load (VL) and CD4+ T cell count are widely used as biomarkers of HIV type 1 (HIV-1) replication, pathogenesis, and response to antiretroviral therapy (ART). However, the clinical potential of cell-associated (CA) HIV-1 molecular markers is much less understood. Here, we measured CA HIV-1 RNA and DNA in HIV-infected individuals treated with temporary ART initiated during primary HIV-1 infection. We demonstrate substantial predictive value of CA RNA for (a) the virological and immunological response to early ART, (b) the magnitude and time to viral rebound after discontinuation of early ART, and (c) disease progression in the absence of treatment. Remarkably, when adjusted for CA RNA, plasma VL no longer appeared as an independent predictor of any clinical endpoint in this cohort. The potential of CA RNA as an HIV-1 clinical marker, in particular as a predictive biomarker of virological control after stopping ART, should be explored in the context of HIV-1 curative interventions.
血浆病毒载量(VL)和 CD4+T 细胞计数被广泛用作 HIV 型 1(HIV-1)复制、发病机制和抗逆转录病毒治疗(ART)反应的生物标志物。然而,细胞相关(CA)HIV-1 分子标志物的临床潜力还不太了解。在这里,我们测量了在原发性 HIV-1 感染期间接受临时 ART 治疗的 HIV 感染者的 CA HIV-1 RNA 和 DNA。我们证明 CA RNA 具有很大的预测价值,可预测(a)早期 ART 的病毒学和免疫学反应,(b)早期 ART 停止后病毒反弹的程度和时间,以及(c)无治疗时的疾病进展。值得注意的是,当根据 CA RNA 进行调整时,血浆 VL 不再作为该队列中任何临床终点的独立预测因子。CA RNA 作为 HIV-1 临床标志物的潜力,特别是作为停止 ART 后病毒学控制的预测生物标志物,应在 HIV-1 治愈干预的背景下进行探索。