Grovit-Ferbas K, Ferbas J, Gudeman V, Sadeghi S, Goetz M B, Giorgi J V, Chen I S, O'Brien W A
Division of Hematology-Oncology, Department of Medicine, UCLA School of Medicine and UCLA AIDS Institute, Los Angeles, California 90095-1678, USA.
J Virol. 1998 Nov;72(11):8650-8. doi: 10.1128/JVI.72.11.8650-8658.1998.
The lack of clinical progression in some individuals despite prolonged human immunodeficiency virus type 1 (HIV-1) infection may result from infection with less-pathogenic viral strains. To address this question, we examined the HIV-1 envelope protein from a donor with a low viral burden, stable CD4(+) T-lymphocyte counts, and little evidence of CD8(+) T-cell expansion, activation, or immune activity. To avoid potential changes in envelope function resulting from selection in vitro, envelope clones were constructed by using viral RNA isolated from uncultured peripheral blood mononuclear cells (PBMC). The data showed that recombinant viruses containing envelope sequences derived from RNA isolated from patient PBMC replicated poorly in primary CD4(+) T cells but demonstrated efficient growth in macrophages. The unusual phenotype of these viruses could not be explained solely by differential utilization of coreceptors since the chimeric viruses, as well as an uncloned isolate obtained from the same visit date, can utilize CCR5. In addition, the donor's own cells appeared resistant to infection with chimeric viruses containing autologous envelope sequences. Genotype analysis revealed that the donor was heterozygous for the previously described 32-bp deletion in CCR5 which may be linked with prolonged survival in HIV-1-infected individuals. These data suggest that the changes in envelope sequences confer properties of viral attenuation, which together with the CCR5 +/Delta32 genotype could account for the long-term survival of this patient.
尽管感染了人类免疫缺陷病毒1型(HIV-1)很长时间,但一些个体缺乏临床进展可能是由于感染了致病性较低的病毒株。为了解决这个问题,我们研究了一位病毒载量低、CD4(+) T淋巴细胞计数稳定且几乎没有CD8(+) T细胞扩增、激活或免疫活性证据的供体的HIV-1包膜蛋白。为避免体外选择导致包膜功能发生潜在变化,通过使用从未培养的外周血单核细胞(PBMC)中分离的病毒RNA构建包膜克隆。数据显示,含有从患者PBMC分离的RNA衍生的包膜序列的重组病毒在原代CD4(+) T细胞中复制不佳,但在巨噬细胞中显示出高效生长。这些病毒的异常表型不能仅通过共受体的差异利用来解释,因为嵌合病毒以及从同一就诊日期获得的未克隆分离株都可以利用CCR5。此外,供体自身的细胞似乎对含有自体包膜序列的嵌合病毒感染具有抗性。基因型分析显示,供体对于先前描述的CCR5中32碱基对缺失是杂合的,这可能与HIV-1感染个体的长期存活有关。这些数据表明,包膜序列的变化赋予了病毒减毒特性,这与CCR5 +/Delta32基因型一起可以解释该患者的长期存活。