咪喹莫特及其羟基化代谢物R-842体外诱导人血细胞中干扰素和其他细胞因子的研究

C E Weeks, S J Gibson
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引用次数: 107

摘要

低分子量免疫调节剂候选药物咪喹莫特(R-837)及其羟基化代谢物R-842在体外测试中浓度为0.5微克/毫升或更高时,可诱导人血细胞中的干扰素- α (ifn - α)。发现ifn - α的量随孵育时间的增加而增加,从2-6小时到24-48小时,并且依赖于细胞数量和药物浓度。这两种化学物质在人外周血单核细胞(PBMC)培养中产生的ifn - α比平行测试的其他已知诱导剂更多。他们还在体外培养的人PBMC中诱导了可检测量的白细胞介素(IL)-1、IL-6、IL-8和肿瘤坏死因子- α。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Induction of interferon and other cytokines by imiquimod and its hydroxylated metabolite R-842 in human blood cells in vitro.

The low-molecular-weight immunomodulator drug candidate, imiquimod (R-837), and its hydroxylated metabolite R-842, induce interferon-alpha (IFN-alpha) in human blood cells in vitro when tested in concentrations of 0.5 microgram/ml or more. The amounts of IFN-alpha found increased with time from 2-6 h of incubation up to 24-48 h, and were dependent on cell number and drug concentration. These two chemicals yielded more IFN-alpha in human peripheral blood mononuclear cell (PBMC) cultures than other known inducers tested in parallel. They also induced detectable amounts of interleukin (IL)-1, IL-6, IL-8, and tumor necrosis factor-alpha in human PBMC cultures in vitro.

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