Sprecher E, Becker Y
Department of Molecular Virology, Faculty of Medicine, Hebrew University, Jerusalem, Israel.
Arch Virol. 1990;110(3-4):259-69. doi: 10.1007/BF01311294.
Macrophages have been shown to play a determining role in the immune defense against herpes simplex virus-1 (HIV-1) intraperitoneal infection in the mouse. In the present study, the effect of HSV-1 infection on interleukin-1 alpha and beta gene transcription in peritoneal exudate cells was investigated. HSV-1 infection was found to induce interleukin-1 alpha and beta gene transcription in these cells. Induction of the interleukin-1 beta gene initiated 6 h postinfection (p.i.) and terminated at 48 h p.i. In contrast, interleukin-1 alpha RNA was detectable at high levels at 6h p.i. but not at 24 h p.i. Inactivation of virus prior to infection prevented HSV-1-induced IL-1 gene induction, indicating that only infectious virus is able to stimulate IL-1 gene transcription. These findings are discussed in relation to the role of macrophages in the immunological mechanisms of defense against HSV-1 infection.
巨噬细胞已被证明在小鼠抗单纯疱疹病毒1型(HSV-1)腹腔感染的免疫防御中起决定性作用。在本研究中,研究了HSV-1感染对腹腔渗出细胞中白细胞介素-1α和β基因转录的影响。发现HSV-1感染可诱导这些细胞中的白细胞介素-1α和β基因转录。白细胞介素-1β基因的诱导在感染后6小时开始,在感染后48小时终止。相比之下,白细胞介素-1αRNA在感染后6小时可高水平检测到,但在感染后24小时未检测到。感染前病毒的灭活可阻止HSV-1诱导的IL-1基因诱导,表明只有感染性病毒能够刺激IL-1基因转录。结合巨噬细胞在抗HSV-1感染免疫机制中的作用对这些发现进行了讨论。