Williams T W
Lymphokine Res. 1984 Spring;3(3):113-8.
Our recent studies have demonstrated a significant enhancement of human lymphotoxin (LT) induced in vitro target cell killing by human alpha and beta interferons (IFN), including highly purified recombinant DNA-produced IFN. This synergistic effect of IFN on LT activity was dose dependent, observed with as little as 10 U/ml IFN, was demonstrable on human normal and tumor cells, and was blocked by treatment with antiserum to IFN. When IFNs and target cells from other animal species were tested, 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. These results describe a new property of IFN in lymphocyte-mediated target cell killing and are discussed in relationship to previously observed enhancing and protective effects of IFN in natural killer (NK) cell systems, as well as to the role of IFN in viral infection.
我们最近的研究表明,人α和β干扰素(IFN),包括高度纯化的重组DNA产生的IFN,可显著增强人淋巴毒素(LT)在体外诱导的靶细胞杀伤作用。IFN对LT活性的这种协同作用是剂量依赖性的,低至10 U/ml的IFN即可观察到,在人正常细胞和肿瘤细胞上均可证实,并且可被抗IFN血清处理所阻断。当测试来自其他动物物种的IFN和靶细胞时,有一项新发现表明IFN对人LT活性具有保护作用。IFN诱导的增强或保护作用取决于特定的IFN:靶细胞组合,在同源人组合中观察到的增强程度最高。这些结果描述了IFN在淋巴细胞介导的靶细胞杀伤中的一种新特性,并结合之前在自然杀伤(NK)细胞系统中观察到的IFN的增强和保护作用以及IFN在病毒感染中的作用进行了讨论。