University of North Carolina HIV Cure Center, University of North Carolina Chapel Hill School of Medicine, Chapel Hill, North Carolina, USA.
Department of Medicine, University of North Carolina Chapel Hill School of Medicine, Chapel Hill, North Carolina, USA.
J Infect Dis. 2022 Mar 2;225(5):856-861. doi: 10.1093/infdis/jiab487.
We tested the combination of a broadly neutralizing HIV antibody with the latency reversal agent vorinostat (VOR). Eight participants received 2 month-long cycles of VRC07-523LS with VOR. Low-level viremia, resting CD4+ T-cell-associated HIV RNA (rca-RNA) was measured, and intact proviral DNA assay (IPDA) and quantitative viral outgrowth assay (QVOA) were performed at baseline and posttreatment. In 3 participants, IPDA and QVOA declines were accompanied by significant declines of rca-RNA. However, no IPDA or QVOA declines clearly exceeded assay variance or natural decay. Increased resistance to VRC07-523LS was not observed. This combination therapy did not reduce viremia or the HIV reservoir. Clinical Trials Registration. NCT03803605.
我们测试了广谱中和抗体 VRC07-523LS 与潜伏期逆转剂伏立诺他(VOR)的联合用药。8 名参与者接受了为期 2 个月的 VRC07-523LS 联合 VOR 治疗。在基线和治疗后,我们检测了低水平的病毒血症、静止 CD4+T 细胞相关 HIV RNA(rca-RNA),并进行了完整的前病毒 DNA 检测(IPDA)和定量病毒扩增检测(QVOA)。在 3 名参与者中,IPDA 和 QVOA 的下降伴随着 rca-RNA 的显著下降。然而,没有任何 IPDA 或 QVOA 的下降明显超过了检测的变异性或自然衰减。也没有观察到对 VRC07-523LS 的耐药性增加。这种联合治疗并没有降低病毒血症或 HIV 储存库。临床试验注册。NCT03803605。