Williams T W, Bellanti J A
Cell Immunol. 1984 Feb;83(2):255-61. doi: 10.1016/0008-8749(84)90304-6.
In a previous study it was reported that human alpha-interferons (IFN) caused a significant enhancement of human lymphotoxin (LT)-induced in vitro killing of human target cells. This synergistic effect was dose dependent and was demonstrable on normal and tumor cell targets. The effects of IFNs from human and several animal species on human LT-induced cell killing of human, mouse, and rabbit target cells are examined. In addition to enhancement of IFN, a new finding was made showing protective effects of IFN on human LT activity. IFN-induced enhancement or protection depended on the particular IFN:target cell combination, with the highest degree of enhancement being observed in the homologous human combination. In this latter case, IFN-induced enhancement was blocked by antiserum to IFN. While a role for other soluble factors cannot be ruled out, the results suggest that, in the homologous human system, enhancement of LT activity was mediated by IFN. These results are discussed in relationship to previously observed enhancing and protective effects of IFN in natural killer cell systems.
在先前的一项研究中报告称,人α干扰素(IFN)可显著增强人淋巴毒素(LT)在体外对人靶细胞的杀伤作用。这种协同效应呈剂量依赖性,在正常细胞和肿瘤细胞靶标上均可得到证实。本文研究了来自人及几种动物物种的IFN对人LT诱导的人、小鼠和兔靶细胞杀伤作用的影响。除了增强作用外,还发现了IFN对人LT活性具有保护作用这一新现象。IFN诱导的增强或保护作用取决于特定的IFN:靶细胞组合,在同源的人组合中观察到的增强程度最高。在后一种情况下,IFN诱导的增强作用被IFN抗血清阻断。虽然不能排除其他可溶性因子的作用,但结果表明,在同源的人系统中,LT活性的增强是由IFN介导的。本文结合先前在自然杀伤细胞系统中观察到的IFN的增强和保护作用对这些结果进行了讨论。