Corssmit E P, Heijligenberg R, Hack C E, Endert E, Sauerwein H P, Romijn J A
Department of Internal Medicine, Academic Medical Centre, University of Amsterdam, The Netherlands.
Clin Exp Immunol. 1997 Feb;107(2):359-63. doi: 10.1111/j.1365-2249.1997.269-ce1161.x.
Plasma concentrations of IFN-alpha are increased in several inflammatory conditions. Several lines of evidence indicate that IFN-alpha has anti-inflammatory properties. To study the effects of IFN-alpha on leucocyte subsets and activation and on cytokines, we administered IFN-alpha (rhIFN-alpha2b; 5 x 10(6) U/m2) to eight healthy human subjects in a randomized controlled cross-over study and analysed changes in circulating leucocytes and parameters for neutrophil and monocyte activation. After administration of IFN-alpha, neutrophil counts increased, monocyte counts decreased transiently, whereas the number of lymphocytes, basophils and eosinophils showed a sustained decrease. IFN-alpha administration was also associated with neutrophil activation, reflected in an increase in the plasma concentrations of elastase-alpha1-antitrypsin complexes and lactoferrin. Serum neopterin, a marker for monocyte activation, was significantly increased 10 h after administration of IFN-alpha. IFN-alpha significantly increased plasma concentrations of IL-6, IL-8 and IL-10. Although IL-1 and tumour necrosis factor (TNF) remained undetectable, plasma concentrations of soluble TNF receptors p55 and p75 increased after IFN-alpha administration. We conclude that IFN-alpha induces multiple alterations in the distribution and functional properties of leucocytes. IFN-alpha exerts pro- as well as anti-inflammatory effects within the cytokine network.
在多种炎症状态下,血浆中α干扰素(IFN-α)的浓度会升高。多项证据表明,IFN-α具有抗炎特性。为了研究IFN-α对白细胞亚群、激活情况以及细胞因子的影响,我们在一项随机对照交叉研究中,对8名健康人类受试者给予IFN-α(重组人IFN-α2b;5×10⁶U/m²),并分析循环白细胞的变化以及中性粒细胞和单核细胞激活的参数。给予IFN-α后,中性粒细胞计数增加,单核细胞计数短暂下降,而淋巴细胞、嗜碱性粒细胞和嗜酸性粒细胞的数量持续减少。给予IFN-α还与中性粒细胞激活有关,这表现为α1-抗胰蛋白酶-弹性蛋白酶复合物和乳铁蛋白的血浆浓度增加。血清新蝶呤是单核细胞激活的标志物,在给予IFN-α后10小时显著升高。IFN-α显著增加了IL-6、IL-8和IL-10的血浆浓度。尽管未检测到IL-1和肿瘤坏死因子(TNF),但给予IFN-α后,可溶性TNF受体p55和p75的血浆浓度升高。我们得出结论,IFN-α可诱导白细胞在分布和功能特性方面发生多种改变。IFN-α在细胞因子网络中发挥促炎和抗炎作用。