Wallach D
Cell Immunol. 1983 Feb 1;75(2):390-5. doi: 10.1016/0008-8749(83)90337-4.
HeLa cells show a decrease of susceptibility to the killing by natural killer (NK) cells when treated with IFN-alpha, beta, or gamma. The concentrations at which preparations of IFN-alpha or beta induce the resistance to killing are those which also induce resistance of HeLa cells to infection by vesicular stomatitis virus (VSV). Stimulation of the killing activity of NK cells is also induced at that same range of concentrations of IFN-alpha and beta. In contrast with preparations of IFN-gamma, induction of the resistance to killing occurs at IFN concentrations which have only marginal stimulatory effect on the activity of NK cells and have no antiviral effect against VSV. IFN-gamma, produced with cloned IFN-gamma cDNA, is as effective as lymphocyte-produced IFN in inducing the resistance to natural killing. The potent effect of IFN-gamma on the target cells is, therefore, not due to the function of lymphokines which might contaminate lymphocyte-produced preparations of IFN-gamma, but a genuine property of the IFN itself.
当用α、β或γ干扰素处理时,HeLa细胞对自然杀伤(NK)细胞杀伤作用的敏感性降低。α或β干扰素制剂诱导抗杀伤作用的浓度,也是诱导HeLa细胞对水泡性口炎病毒(VSV)感染产生抗性的浓度。在相同浓度范围内的α和β干扰素也能刺激NK细胞的杀伤活性。与γ干扰素制剂相反,诱导抗杀伤作用的γ干扰素浓度对NK细胞活性只有微弱的刺激作用,且对VSV没有抗病毒作用。用克隆的γ干扰素cDNA产生的γ干扰素,在诱导抗自然杀伤方面与淋巴细胞产生的干扰素一样有效。因此,γ干扰素对靶细胞的强大作用不是由于可能污染淋巴细胞产生的γ干扰素制剂的淋巴因子的功能,而是干扰素本身的固有特性。