Dhawan S, Heredia A, Lal R B, Wahl L M, Epstein J S, Hewlett I K
Laboratory of Molecular Virology, Food and Drug Administration (HFM-310), Rockville, MD 20852.
Biochem Biophys Res Commun. 1994 Jun 15;201(2):756-61. doi: 10.1006/bbrc.1994.1765.
Treatment of monocytes with interferon-gamma 1 day before, or at the time of infection with human immunodeficiency virus type-1 (HIV-1) induced complete resistance in monocytes against HIV-1 infection. There was no evidence of viral RNA, proviral DNA, p24 antigen, or reverse transcriptase activity through 2 weeks after inoculation. Ultrastructural examination of these cells showed no detectable virus particles. When interferon-gamma was added to monocytes 1 to 3 days post-infection, virus integration occurred, but the viral expression was either ablated (1 day post-infection) or significantly inhibited (3 days post-infection). Treatment of monocytes with interferon-gamma before or after infection with HIV-1 produced significantly higher levels of tumor necrosis factor-alpha and interleukin-8 than untreated or uninfected monocytes. These results suggest that altered regulation of cytokines may mediate antiviral activity of interferon-gamma in monocytes.
在用1型人类免疫缺陷病毒(HIV-1)感染前1天或感染时用γ干扰素处理单核细胞,可诱导单核细胞对HIV-1感染产生完全抗性。接种后2周内均未检测到病毒RNA、前病毒DNA、p24抗原或逆转录酶活性。对这些细胞进行超微结构检查未发现可检测到的病毒颗粒。当在感染后1至3天向单核细胞中添加γ干扰素时,病毒发生整合,但病毒表达要么被消除(感染后1天),要么受到显著抑制(感染后3天)。在HIV-1感染之前或之后用γ干扰素处理单核细胞,与未处理或未感染的单核细胞相比,可产生显著更高水平的肿瘤坏死因子-α和白细胞介素-8。这些结果表明,细胞因子调节的改变可能介导了γ干扰素在单核细胞中的抗病毒活性。