Fleischmann W R
Tex Rep Biol Med. 1977;35:316-25.
Pretreatment of L cell cultures with low levels of mouse interferon caused a more rapid development of and a greater degree of protection with subsequent exposure to higher levels of mouse interferon than that observed for control cultures. Such priming was a specific event which required cellular RNA synthesis. Priming by mouse fibroblast interferon, mouse immune interferon, and human leukocyte interferon was directly related to the plaque reduction titer of each of the interferons on L cells.
用低水平的小鼠干扰素预处理L细胞培养物，与对照培养物相比，随后暴露于高水平的小鼠干扰素时，会导致更快的发育和更高程度的保护。这种引发是一个需要细胞RNA合成的特定事件。小鼠成纤维细胞干扰素、小鼠免疫干扰素和人白细胞干扰素的引发与每种干扰素对L细胞的蚀斑减少效价直接相关。
