Huang Y, Zhang L, Ho D D
Aaron Diamond AIDS Research Center, New York University School of Medicine, New York 10016.
J Virol. 1995 Jan;69(1):93-100. doi: 10.1128/JVI.69.1.93-100.1995.
Studies with the simian immunodeficiency virus have shown that nef deletion results in a low level of viremia and a lack of disease progression in monkeys. Given the similarity of this clinical profile to that observed in long-term survivors of human immunodeficiency virus type 1 (HIV-1) infection, we sought to examine the nef gene in 10 patients who are clinically healthy and immunologically normal despite 12 to 15 years of infection. PCR and DNA sequencing were used to determine nef sequences in peripheral blood mononuclear cells obtained from long-term survivors. We found that there is no gross deletion within nef in the cases studied; most nef sequences (91.1%) obtained from 10 subjects contained a full-length and intact open reading frame. In addition, at the protein level, there were no discernible differences between the Nef consensus sequences derived from long-term survivors and those from patients with AIDS. We therefore conclude that deletion of or gross sequence abnormality within nef is not likely to be a common explanation for the well-being of long-term survivors of HIV-1 infection. Moreover, phylogenetic analysis of nef sequences suggests that HIV-1 strains found in our study subjects do not have a common origin.
对猿猴免疫缺陷病毒的研究表明,nef基因缺失会导致猴子体内病毒血症水平较低且疾病无进展。鉴于这种临床特征与1型人类免疫缺陷病毒(HIV-1)感染长期存活者中观察到的情况相似,我们试图检测10名患者的nef基因,这些患者尽管已感染12至15年,但临床健康且免疫功能正常。采用聚合酶链反应(PCR)和DNA测序来确定从长期存活者获取的外周血单个核细胞中的nef序列。我们发现,在所研究的病例中,nef基因没有明显缺失;从10名受试者获得的大多数nef序列(91.1%)包含全长且完整的开放阅读框。此外,在蛋白质水平上,长期存活者的Nef共有序列与艾滋病患者的Nef共有序列之间没有明显差异。因此,我们得出结论,nef基因缺失或序列严重异常不太可能是HIV-1感染长期存活者健康状况良好的常见原因。此外,nef序列的系统发育分析表明,我们研究对象中发现的HIV-1毒株没有共同起源。