The effect of dendritic cells on proliferation and anti-tumor activity against leukemia of cytokine induced killer cells
Xiaoyun Lian
Abstract
Xiaoyun Lian
Abstract
Objective The purpose was to investigate the effect of dendritic cells(DC) on proliferation,phenotype,secretory cytokines and anti-tumor activity against leukemia cells of cytokine-induced killer cells(CIK).Methods DC and CIK were prepared from healthy human peripheral blood mononuclear cells.They were co-cultured.CIK cells were cultured alone as control.Increased number of cells were counted by tapan-blue staining,killing activity was detected by MTT assay,cells phenotypes were analyzed by flow cytometry,secretions of INF-γ,IL-12 were determined by ELISA.Results The proliferation activity of DC-CIK cells was significantly higher than that of CIK cells(P0.05);Under the same condition,the rate of CD3+CD56+ and CD3+CD8+ double positive cells in CIK cells were significantly enhanced by co-cultured with DC(P0.05);In DC-CIK cells,the level of IL-12,INF-γ in culture supernatants were all increased noticeably on day 3 compared to CIK cells which were cultured alone(P0.01,P0.05);At the effector-target ratio from 5:1 to 40:1,the anti-tumor effect of DC-CIK cells was much higher than that of CIK cells(P0.05),and this effect was positive related with the effector-target ratio.Conclusion The proliferation activity,anti-tumor effects against leukemia cells of DC-CIK cells were significantly higher than that of CIK cells.DC-CIK is promising as an immuno-therapeutic strategy for patients leukemia.
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Objective The purpose was to investigate the effect of dendritic cells(DC) on proliferation,phenotype,secretory cytokines and anti-tumor activity against leukemia cells of cytokine-induced killer cells(CIK).Methods DC and CIK were prepared from healthy human peripheral blood mononuclear cells.They were co-cultured.CIK cells were cultured alone as control.Increased number of cells were counted by tapan-blue staining,killing activity was detected by MTT assay,cells phenotypes were analyzed by flow cytometry,secretions of INF-γ,IL-12 were determined by ELISA.Results The proliferation activity of DC-CIK cells was significantly higher than that of CIK cells(P0.05);Under the same condition,the rate of CD3+CD56+ and CD3+CD8+ double positive cells in CIK cells were significantly enhanced by co-cultured with DC(P0.05);In DC-CIK cells,the level of IL-12,INF-γ in culture supernatants were all increased noticeably on day 3 compared to CIK cells which were cultured alone(P0.01,P0.05);At the effector-target ratio from 5:1 to 40:1,the anti-tumor effect of DC-CIK cells was much higher than that of CIK cells(P0.05),and this effect was positive related with the effector-target ratio.Conclusion The proliferation activity,anti-tumor effects against leukemia cells of DC-CIK cells were significantly higher than that of CIK cells.DC-CIK is promising as an immuno-therapeutic strategy for patients leukemia.
Key concepts: Cytokine-induced killer cell, Flow cytometry, K562 cells, Leukemia, Peripheral blood mononuclear cell, MTT assay, Cytokine, CD8