各种因素对人白细胞培养中α -干扰素产生的影响。

D M Katschinski, P Neustock, H Klüter, H Kirchner
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引用次数: 18

摘要

已知诱导剂特异性基因位点和性别在小鼠干扰素α (ifn - α)产生的调节中发挥作用。由于对人类ifn - α系统的遗传控制知之甚少,我们通过用新城疫病毒(NDV)或仙台病毒(SDV)培养外周血,研究了468个人的ifn - α产生情况。不同供体的IFN α释放量差异很大。然而,在4个月的时间里,7个供体的ifn - α产生显示出供体特异性反应,这使我们将一些供体分为高反应和低反应。NDV诱导量与SDV诱导量呈正相关。供体的性别并没有显著改变ifn - α的产生。受试者年龄在1岁到90岁之间。ifn - α水平在儿童中最高,随后随着年龄的增长逐渐下降。使用特异性ifn - α -2酶联免疫吸附试验(ELISA)和生物测定法检测所有亚型,我们的数据显示,ifn - α的净产量随着年龄的增长而下降。为了进一步研究,我们选择了17个低生产者和17个高生产者。为了分析主要组织相容性复合体(MHC)对ifn - α产生的可能影响,我们测定了13个低产生者和12个高产生者的HLA基因型。在这里,没有检测到高或低产量与HLA基因型的相关性。
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Influence of various factors on interferon-alpha production in cultures of human leukocytes.

Inducer-specific gene loci and sex are known to play a role in the regulation of interferon-alpha (IFN-alpha) production in mice. Because little is known about the genetic control of the IFN-alpha system in man, we investigated the IFN-alpha production of 468 individuals by culturing peripheral blood with Newcastle disease virus (NDV) or Sendai virus (SDV). The IFN alpha release of different donors varied over a wide range. However, IFN-alpha production of 7 donors showed a donor-specific response over a period of 4 months, which led us to classify some donors as high and low responders. The amounts induced by NDV correlated positively to those induced by SDV. The donor's sex did not alter the IFN-alpha production significantly. The subjects were between 1 and 90 years in age. Highest IFN-alpha levels were obtained in children, followed by a gradual decline with age. Using a specific IFN-alpha-2 enzyme-linked immunosorbent assay (ELISA) and a bioassay, which detects all subtypes, our data showed that the net IFN-alpha production decreased with age. For further studies, we selected 17 low producers and 17 high producers. To analyze a possible influence of major histocompatibility complex (MHC) on IFN-alpha production, the HLA genotypes of 13 low producers and 12 high producers were determined. Here, no correlation between high or low production and HLA genotype was detectable.

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