Li C, Yan W, Hao Y, Feng S, Qiu L, Liu H, Han J, Li X, Feng S
Institute of Hematology and Blood Diseases Hospital, CAMS and PUMC, Tianjin 300020.
Zhonghua Xue Ye Xue Za Zhi. 1997 Aug;18(8):410-2.
To evaluate the killing effect of IL-2 and IFN-alpha activated bone marrow cells on K562 cells.
Semi-solid colony assay was used.
Bone marrow from leukemia patients in remission was activated in vitro with IL-2 for 3 days. The activated bone marrow (ABM) displayed killing effects of 0.31 approximately 2.30 logs on K562 cells, this killing effects was further increased to 0. 30 approximately > 3.15 logs when IFN-alpha added with IL-2 to the marrow for activation. IL-2 alone or in combination with IFN-alpha showed no inhibition of CFU-GM and K562 cells. Compared with IL-2 or IFN-alpha alone, the combination of the two cytokines could more effectively maintain the killing effect of ABM on leukemic cells.
IFN-alpha can augment the purging effect of IL-2 ABM and combination of the two cytokines can effectively maintain the cytotoxicity of ABM.
评估白细胞介素-2(IL-2)和α干扰素(IFN-α)激活的骨髓细胞对K562细胞的杀伤作用。
采用半固体集落分析法。
白血病缓解期患者的骨髓在体外经IL-2激活3天。激活的骨髓(ABM)对K562细胞显示出0.31至约2.30对数的杀伤作用,当在骨髓激活时将IFN-α与IL-2一起添加,这种杀伤作用进一步增加至0.30至约>3.15对数。单独的IL-2或与IFN-α联合使用均未显示对CFU-GM和K562细胞有抑制作用。与单独使用IL-2或IFN-α相比,两种细胞因子联合使用能更有效地维持ABM对白血病细胞的杀伤作用。
IFN-α可增强IL-2激活的ABM的净化作用,两种细胞因子联合使用能有效维持ABM的细胞毒性。