Stewart W E, De Clercq E, De Somer P
J Virol. 1972 Nov;10(5):896-901. doi: 10.1128/JVI.10.5.896-901.1972.
A system is described for assaying mouse interferon without using a viral "challenge" agent. Interferon-treated L cells were destroyed by exposure to polyriboinosinic.polyribocytidylic acid [poly(I).poly(C)], and the amount of destruction was dependent on both the concentration of interferon to which the cells were exposed and the amount of poly(I).poly(C) used as the "challenge" material. If the amount of poly(I).poly(C) was constant, the concentration of interferon could be determined by quantitating cell destruction 6 hr after addition of the double-stranded ribonucleic acid. In addition to eliminating the necessity for employing infectious virus for interferon assays, this system has the advantages of being quicker, easier, and more sensitive than other interferon assays. The sensitivity of the assay is related directly to the amount of poly(I).poly(C) applied to the cells, with each fivefold increase of poly(I).poly(C) giving about a fivefold increase of sensitivity.
描述了一种用于测定小鼠干扰素的系统,该系统不使用病毒“攻击”剂。经干扰素处理的L细胞通过暴露于聚肌苷酸·聚胞苷酸[聚(I)·聚(C)]而被破坏,破坏量取决于细胞所暴露的干扰素浓度以及用作“攻击”材料的聚(I)·聚(C)的量。如果聚(I)·聚(C)的量恒定,则可以通过在加入双链核糖核酸6小时后对细胞破坏进行定量来确定干扰素的浓度。除了消除在干扰素测定中使用感染性病毒的必要性外,该系统还具有比其他干扰素测定更快、更容易且更灵敏的优点。该测定的灵敏度与应用于细胞的聚(I)·聚(C)的量直接相关,聚(I)·聚(C)每增加五倍,灵敏度大约增加五倍。