Torsteinsdottir S, Masucci M G, Bejarano M T, Berthold W, Klein E, Klein G
Cell Immunol. 1985 Jan;90(1):65-73. doi: 10.1016/0008-8749(85)90169-8.
Recombinant human interferon alpha (IFN-alpha) and interferon gamma (IFN-gamma) were compared for their ability to influence the proliferative capacity of tumor-derived cell lines and of normal B lymphocytes infected in vitro by Epstein-Barr virus (EBV). EBV-induced B-cell proliferation was suppressed almost completely when 10(2) U/ml IFN-alpha were added to the culture medium while the same dose of IFN-gamma had significantly lower inhibitory activity. The pure IFNs differed in their ability to influence the growth of three Burkitt lymphoma-derived cell lines, Raji, Daudi, and Namalwa, depending on whether the cells were propagated in suspension or in semisolid cultures. IFN-alpha inhibited cell proliferation under both culture conditions with thresholds of sensitivity characteristics for each cell line. In contrast, IFN-gamma had no effect on the growth in suspension but it abolished the clonogenic potential of tumor cell lines in semisolid agarose. The results suggest that the two IFN types may exert their growth inhibitory activity through different mechanisms of action.
对重组人α干扰素(IFN-α)和γ干扰素(IFN-γ)影响肿瘤来源细胞系以及体外受爱泼斯坦-巴尔病毒(EBV)感染的正常B淋巴细胞增殖能力进行了比较。当向培养基中添加10² U/ml IFN-α时,EBV诱导的B细胞增殖几乎被完全抑制,而相同剂量的IFN-γ的抑制活性则显著较低。根据细胞是在悬浮培养还是半固体培养中生长,这两种纯干扰素影响三种伯基特淋巴瘤来源细胞系(拉吉、道迪和纳马瓦)生长的能力有所不同。在两种培养条件下,IFN-α均抑制细胞增殖,且每种细胞系都有其敏感性特征阈值。相比之下,IFN-γ对悬浮生长没有影响,但它消除了肿瘤细胞系在半固体琼脂糖中的克隆形成潜力。结果表明,这两种类型的干扰素可能通过不同的作用机制发挥其生长抑制活性。