Lutton J D, Levere R D
J Lab Clin Med. 1980 Aug;96(2):328-33.
The suppressive effect of two types of human interferon (fibroblast and leukocyte types) on bone marrow and peripheral blood erythroid colony formation by cells from patients with various disorders of erythropoiesis was studied. Bone marrow or peripheral blood mononuclear cells were isolated and cultured in plasma clots with Epo, and benzidine-positive erythroid colonies counted after 7 to 14 days' incubation. Specimens included cells from patients with thalassemia, sickle cell anemia, secondary polycythemia, nutritional anemia, hemolytic anemia, refractory anemia, and normal controls. Results show that with the exception of nutritional anemia cells, erythroid colony formation by all specimens was significantly inhibited (84% to 100%) by 100 to 200 U of either interferon type per milliliter. Erythroid colony formation by nutritional anemia bone marrow cells ws inhibited only 30% to 40% by 200 U/ml fibroblast or leukocyte interferon, and 100 U/ml were ineffective. Sickle cell peripheral blood mononuclear cells and refractory anemia bone marrow demonstrated marked inhibition of colony formation (86% to 97%) with 50 U/ml fibroblast or leukocyte interferon. Inhibition of colony formation by sickle cell peripheral blood mononuclear cells was completely abolished by addition of anti-interferon. Colony formation by refractory anemia bone marrow was inhibited 46% to 51% by as little as 10 U/ml fibroblast or leukocyte interferon. This concentration of interferon was ineffective with cells from thalassemia, secondary polycythemia, nutritional anemia, hemolytic anemia, and controls. Mouse bone marrow colony formation was not suppressed by 200 U/ml leukocyte interferon. These results demonstrate that fibroblast or leukocyte interferons inhibit in vitro erythroid colony formation by human bone marrow or peripheral blood mononuclear cells, the effect is abolished by anti-interferon, and inhibition may be species-specific. These studies reveal that cells obtained from certan patients are particularly sensitive to the cytoxic effects of interferon, and it may be useful to monitor the erythropoietic state of the patient during interferon chemotherapy.
研究了两种类型的人干扰素(成纤维细胞型和白细胞型)对患有各种红细胞生成障碍疾病患者的骨髓及外周血红细胞集落形成的抑制作用。分离骨髓或外周血单个核细胞,与促红细胞生成素(Epo)一起在血浆凝块中培养,孵育7至14天后计数联苯胺阳性红细胞集落。标本包括来自地中海贫血、镰状细胞贫血、继发性红细胞增多症、营养性贫血、溶血性贫血、难治性贫血患者的细胞以及正常对照。结果显示,除营养性贫血细胞外,每毫升100至200单位的任何一种干扰素均可显著抑制(84%至100%)所有标本的红细胞集落形成。200单位/毫升的成纤维细胞或白细胞干扰素仅抑制营养性贫血骨髓细胞的红细胞集落形成30%至40%,100单位/毫升则无效。50单位/毫升的成纤维细胞或白细胞干扰素可显著抑制镰状细胞外周血单个核细胞和难治性贫血骨髓的集落形成(86%至97%)。加入抗干扰素后,镰状细胞外周血单个核细胞的集落形成抑制作用完全消除。低至10单位/毫升的成纤维细胞或白细胞干扰素可抑制难治性贫血骨髓的集落形成46%至51%。该浓度的干扰素对来自地中海贫血、继发性红细胞增多症、营养性贫血、溶血性贫血患者的细胞及对照无效。200单位/毫升的白细胞干扰素不抑制小鼠骨髓集落形成。这些结果表明,成纤维细胞或白细胞干扰素可抑制人骨髓或外周血单个核细胞的体外红细胞集落形成,抗干扰素可消除该作用,且抑制作用可能具有种属特异性。这些研究表明,某些患者的细胞对干扰素的细胞毒性作用特别敏感,在干扰素化疗期间监测患者的红细胞生成状态可能有用。