Cara A, Vargas J, Keller M, Jones S, Mosoian A, Gurtman A, Cohen A, Parkas V, Wallach F, Chusid E, Gelman I H, Klotman M E
Division of Infectious Disease, Mount Sinai School of Medicine, New York, New York 10029, USA.
Virology. 2002 Jan 5;292(1):1-5. doi: 10.1006/viro.2001.1243.
Closed circular (cc) forms of extrachromosomal HIV DNA are detected in patients with high viral loads; however, it is unclear whether these forms remain if virus replication is suppressed to undetectable levels by combination antiretroviral therapy. A nested primer polymerase chain reaction amplification assay was used to detect the presence of ccDNA containing two long terminal repeat sequences (2-LTR) in PBMC of patients with low or undetectable plasma HIV RNA. Fifty percent of patients with plasma RNA levels <50 copies/ml of blood had detectable 2-LTR DNA. Sequencing of the products identified normal LTR--LTR junctions in the minority of cases with the majority containing anomalies including deletions and insertions. The persistence of HIV ccDNA in patients with no detectable plasma RNA could be consistent with ongoing de novo infection of dividing cells or with stability of this form of DNA in nondividing cells.
在病毒载量高的患者中可检测到染色体外HIV DNA的闭环(cc)形式;然而,尚不清楚如果通过联合抗逆转录病毒疗法将病毒复制抑制到无法检测的水平,这些形式是否会保留。采用巢式引物聚合酶链反应扩增试验检测血浆HIV RNA水平低或无法检测的患者外周血单核细胞中含有两个长末端重复序列(2-LTR)的ccDNA的存在情况。血浆RNA水平<50拷贝/ml血液的患者中有50%可检测到2-LTR DNA。对产物进行测序发现,少数病例中的LTR-LTR连接正常,而大多数病例存在包括缺失和插入在内的异常情况。血浆RNA无法检测的患者中HIV ccDNA的持续存在可能与正在进行的分裂细胞的从头感染或这种DNA形式在非分裂细胞中的稳定性一致。