Johnson C S, Thurlow S M, Marcelletti J F, Furmanski P
Cancer Res. 1986 Aug;46(8):3896-902.
The acute erythroleukemia induced in mice by the anemia-inducing strain of the Friend virus complex is caused to regress by normal macrophages. We examined the possibility that reversal of leukemia is related to a macrophage regulatory function in erythropoiesis. We found that the ability of macrophages to induce leukemia regression correlates with nonimmunological, in vivo suppression of normal and susceptible leukemic erythroid progenitors. The macrophage effect on erythropoiesis appears to be due to changes in a humoral regulator, related to but independent of erythropoietin. The results suggest a novel regulatory system for erythropoiesis, operative in vivo, and involving macrophages as accessory or suppressor cells. This regulation appears to be disrupted in erythroleukemic mice, but can be restored, and the disease can be made to regress by treatment with normal macrophages.
由弗瑞德病毒复合体的致贫血菌株在小鼠中诱发的急性红白血病,可被正常巨噬细胞诱导消退。我们研究了白血病逆转与巨噬细胞在红细胞生成中的调节功能相关的可能性。我们发现,巨噬细胞诱导白血病消退的能力与非免疫性的、体内对正常和易感白血病红系祖细胞的抑制作用相关。巨噬细胞对红细胞生成的影响似乎是由于一种体液调节因子的变化,该调节因子与促红细胞生成素相关但独立于促红细胞生成素。结果提示了一种新的红细胞生成调节系统,在体内发挥作用,且涉及巨噬细胞作为辅助或抑制细胞。这种调节在红白血病小鼠中似乎被破坏了,但可以恢复,并且通过用正常巨噬细胞治疗可使疾病消退。