Martinez-Mariño Beatriz, Foster Hillary, Hao Yanling, Levy Jay A
Department of Medicine, Division Hematology/Oncology, University of California, San Francisco, CA 94143-1270, USA.
Virology. 2007 May 25;362(1):217-25. doi: 10.1016/j.virol.2006.12.007. Epub 2007 Jan 22.
CD8(+) cells from healthy HIV-1-infected individuals suppress human immunodeficiency virus (HIV) replication in infected cells by a non-cytotoxic mechanism. This activity is associated with the production of a soluble CD8(+) cell antiviral factor (CAF) that inhibits viral replication at the level of transcription. Strong CD8(+) cell non-cytotoxic anti-HIV responses (CNARs) correlate with an asymptomatic state and long-term survival of HIV-infected individuals. This antiviral activity is lost when the infected individual advances to disease. In attempts to define the gene(s) mediating CNAR we have evaluated differential gene expression between CD8(+) cells from infected subjects with high CNAR and CD8(+) cells from uninfected controls that lack this activity. The expression analysis, using the Affymetrix GeneChip Human Genome U133 Set, indicated that 18% of the genes were differentially expressed (DE) of which 9.2% were up-regulated. A total of 568 genes were up-regulated with a >2.0-fold difference in expression levels and a >50% concordance of difference call. Stringent selection criteria narrowed down the list to 52 up-regulated 'high confidence genes' (> or = 75% concordance). These genes function in a wide variety of cellular processes and include 13 associated with immunologic activity.
来自健康的HIV-1感染者的CD8(+)细胞通过一种非细胞毒性机制抑制感染细胞中的人类免疫缺陷病毒(HIV)复制。这种活性与一种可溶性CD8(+)细胞抗病毒因子(CAF)的产生有关,该因子在转录水平抑制病毒复制。强烈的CD8(+)细胞非细胞毒性抗HIV反应(CNARs)与HIV感染者的无症状状态和长期生存相关。当感染者病情进展时,这种抗病毒活性就会丧失。为了确定介导CNAR的基因,我们评估了具有高CNAR的感染受试者的CD8(+)细胞与缺乏这种活性的未感染对照的CD8(+)细胞之间的差异基因表达。使用Affymetrix GeneChip Human Genome U133 Set进行的表达分析表明,18%的基因存在差异表达(DE),其中9.2%上调。共有568个基因上调,表达水平差异>2.0倍且差异调用一致性>50%。严格的选择标准将列表缩小到52个上调的“高可信度基因”(一致性≥75%)。这些基因在多种细胞过程中发挥作用,包括13个与免疫活性相关的基因。