首页> 美国卫生研究院文献>Retrovirology >Interferon-α (IFN-α) suppresses HTLV-1 gene expression and cell cycling while IFN-α combined with zidovudin induces p53 signaling and apoptosis in HTLV-1-infected cells
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Interferon-α (IFN-α) suppresses HTLV-1 gene expression and cell cycling while IFN-α combined with zidovudin induces p53 signaling and apoptosis in HTLV-1-infected cells

机译:干扰素-α(IFN-α)抑制HTLV-1基因表达和细胞周期而干扰素-α与齐多夫定联合诱导HTLV-1感染细胞中p53信号传导和凋亡

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摘要

BackgroundHuman T-cell leukemia virus type-1 (HTLV-1) is the causative retrovirus of adult T-cell leukemia/lymphoma (ATL) and HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP). HTLV-1 gene expression is maintained at low levels in vivo by unknown mechanisms. A combination therapy of interferon-α (IFN-α) and zidovudin (AZT) shows therapeutic effects in ATL patients, although its mechanism is also obscure. We previously found that viral gene expression in IL-2-dependent HTLV-1-infected T-cells (ILTs) derived from ATL patients was markedly suppressed by stromal cells through a type I IFN response. Here, we investigated the effects of IFN-α with or without AZT on viral gene expression and cell growth in ILTs.
机译:背景人类1型T细胞白血病病毒(HTLV-1)是成人T细胞白血病/淋巴瘤(ATL)和HTLV-1相关性脊髓病/热带痉挛性轻瘫(HAM / TSP)的病原性逆转录病毒。 HTLV-1基因表达在体内通过未知机制维持在较低水平。干扰素-α(IFN-α)和齐多夫定(AZT)的联合疗法在ATL患者中显示出治疗效果,尽管其机理也不清楚。我们以前发现,来自ATL患者的IL-2依赖性HTLV-1感染的T细胞(ILT)中的病毒基因表达被基质细胞通过I型IFN应答显着抑制。在这里,我们调查了有或没有AZT的IFN-α对ILTs中病毒基因表达和细胞生长的影响。

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