Pierson Theodore C, Kieffer Tara L, Ruff Christian T, Buck Christopher, Gange Stephen J, Siliciano Robert F
Department of Medicine, Johns Hopkins University School of Medicine, Johns Hopkins University School of Public Health, Baltimore, Maryland 21205, USA.
J Virol. 2002 Apr;76(8):4138-44. doi: 10.1128/jvi.76.8.4138-4144.2002.
The development of surrogate markers capable of detecting residual ongoing human immunodeficiency virus type 1 (HIV-1) replication in patients receiving highly active antiretroviral therapy is an important step in understanding viral dynamics and in developing new treatment strategies. In this study, we evaluated the utility of circular forms of the viral genome for the detection of recent infection of cells by HIV-1. We measured the fate of both one-long terminal repeat (1-LTR) and 2-LTR circles following in vitro infection of logarithmically growing CD4+ T cells under conditions in which cell death was not a significant contributing factor. Circular forms of the viral genome were found to be highly stable and to decrease in concentration only as a function of dilution resulting from cell division. We conclude that these DNA circles are not intrinsically unstable in all cell types and suggest that the utility of 2-LTR circle assays in measuring recent HIV-1 infection of susceptible cells in vivo needs to be reevaluated.
开发能够检测接受高效抗逆转录病毒治疗的患者中残留的持续性人类免疫缺陷病毒1型(HIV-1)复制的替代标志物,是理解病毒动力学和制定新治疗策略的重要一步。在本研究中,我们评估了病毒基因组环状形式在检测HIV-1近期细胞感染中的效用。我们在细胞死亡不是显著影响因素的条件下,对数生长的CD4+ T细胞进行体外感染后,测量了单长末端重复序列(1-LTR)和双长末端重复序列(2-LTR)环的命运。发现病毒基因组的环状形式高度稳定,且仅作为细胞分裂导致的稀释作用而浓度降低。我们得出结论,这些DNA环在所有细胞类型中并非本质上不稳定,并建议重新评估2-LTR环检测法在体内测量易感细胞近期HIV-1感染中的效用。