Keating Sheila M, Pilcher Christopher D, Jain Vivek, Lebedeva Mila, Hampton Dylan, Abdel-Mohsen Mohamed, Deng Xutao, Murphy Gary, Welte Alex, Facente Shelley N, Hecht Frederick, Deeks Steven G, Pillai Satish K, Busch Michael P
Blood Systems Research Institute.
Department of Laboratory Medicine.
J Infect Dis. 2017 Jul 1;216(1):72-81. doi: 10.1093/infdis/jix225.
Human immunodeficiency virus (HIV) antibodies are generated and maintained by ongoing systemic expression of HIV antigen. We investigated whether HIV antibody responses as measured by high-throughput quantitative and qualitative assays could be used to indirectly measure persistent HIV replication in individuals receiving antiretroviral therapy (ART).
HIV antibody responses were measured over time in the presence or absence of suppressive ART and were compared to the HIV reservoir size and expression of antiviral restriction factors.
Among untreated individuals, including both elite controllers (ie, persons with a viral load of ≤40 copies/mL) and noncontrollers, antibody parameters were stable over time and correlated with the individual viral load. Viral suppression with ART led to a progressive decline in antibody responses after treatment induction that persisted for 5-7 years. Higher levels of HIV antibodies during suppressive therapy were associated with later initiation of ART after infection, with higher DNA and cell-associated RNA levels, and with lower expression of multiple anti-HIV host restriction factors.
These findings suggest that declining antibody levels during ART reflect lower levels of antigen production and/or viral replication in the persistent HIV reservoir. Results of relatively inexpensive and quantitative HIV antibody assays may be useful indirect markers that enable efficient monitoring of the viral reservoir and suppression during functional-cure interventions.
人类免疫缺陷病毒(HIV)抗体通过HIV抗原的持续全身表达产生并维持。我们研究了通过高通量定量和定性检测所测得的HIV抗体反应是否可用于间接测量接受抗逆转录病毒治疗(ART)的个体中持续的HIV复制。
在有或没有抑制性ART的情况下,随时间测量HIV抗体反应,并将其与HIV储存库大小和抗病毒限制因子的表达进行比较。
在未经治疗的个体中,包括精英控制者(即病毒载量≤40拷贝/毫升的人)和非控制者,抗体参数随时间稳定,且与个体病毒载量相关。ART导致的病毒抑制在治疗开始后使抗体反应逐渐下降,并持续5至7年。抑制性治疗期间较高水平的HIV抗体与感染后较晚开始ART、较高的DNA和细胞相关RNA水平以及多种抗HIV宿主限制因子的较低表达有关。
这些发现表明,ART期间抗体水平下降反映了持续的HIV储存库中抗原产生和/或病毒复制水平较低。相对廉价的定量HIV抗体检测结果可能是有用的间接标志物,可用于在功能性治愈干预期间有效监测病毒储存库和抑制情况。