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Effects of cryopreservation and phenylacetate on biological characters of adherent LAK cells from patients with hepatocellular carcinoma

机译:冷冻保存和苯乙酸对肝细胞癌患者贴壁LAK细胞生物学特性的影响

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摘要

AIM: To improve the preparation of adherent lymphokine-activated killer (A-LAK) cells and to study the effects of cryopreservation and phenylacetate (PA) on biological characters of A-LAK cells.METHODS: A-LAK cells were obtained from peripheral blood mononuclear cells (PBMCs) of the patients with hepatocellular carcinoma (HCC) by using L-phenylalanine methyl ester (PME) to deplete immunosuppressive monocytes. Proliferative activity of SMMC7721 cell line after treatment with phenylacetate (PA) was observed. A-LAK cells were treated with the supernatant of SMMC7721 cells that had been pretreated with PA. The changes of proliferation, cytotoxicity and phenotype of A-LAK cells were investigated after cryopreservation.RESULTS: The expansion of A-LAK cells (96.79 ± 69.10 folds on Day 14) was significantly higher than that of non-adherent LAK (NA-LAK) cells (22.77 ± 13.20) as well as conventional LAK cells (4.64 ± 0.91). PA significantly suppressed the growth of SMMC7721 cells, and the inhibitor ratio was 46%. The supernatant of cultured tumor cells intensively suppressed the proliferation and cytotoxicity of A-LAK cells, but the suppressive effect of the supernatant was previously decreased after treatment with PA. Impairments in proliferation and cytotoxicity of A-LAK cells immediately after thawing of cryopreservation and recovery after reincubation with IL-2 were observed. The cytotoxicity of thawed A-LAK cells on Day 5 was significantly higher than that of fresh A-LAK before freezing (54.8% ± 10.2% vs 40.5% ± 6.4%). No significant change in the percentage of lymphocyte subsets was identified in frozen A-LAK cells as compared with that in the fresh control cells.CONCLUSION: A-LAK cells can be simply prepared by using PME, and showed a synergistic anti-tumor effect with the combination of PA. Cryopreservation can increase the immunoactivities of A-LAK cells from the patients with hepatocellular carcinoma.
机译:目的:为改善贴壁淋巴因子激活的杀伤(A-LAK)细胞的制备,研究冷冻保存和苯乙酸(PA)对A-LAK细胞生物学特性的影响。方法:从外周血中获得A-LAK细胞肝细胞癌(HCC)患者的单核细胞(PBMC),通过使用L-苯丙氨酸甲酯(PME)消耗免疫抑制单核细胞来实现。观察到乙酸苯酯(PA)处理后SMMC7721细胞系的增殖活性。用已经用PA预处理的SMMC7721细胞的上清液处理A-LAK细胞。结果:冷冻后A-LAK细胞的增殖,细胞毒性和表型的变化。结果:A-LAK细胞的扩增(第14天为96.79±69.10倍)明显高于非贴壁LAK(NA-LAK)。 )单元(22.77±13.20)以及常规LAK单元(4.64±0.91)。 PA显着抑制SMMC7721细胞的生长,其抑制率为46%。培养的肿瘤细胞的上清液强烈地抑制了A-LAK细胞的增殖和细胞毒性,但是在用PA处理后,上清液的抑制作用先前降低了。冷冻保存解冻后立即观察到A-LAK细胞的增殖和细胞毒性,并与IL-2重新孵育后恢复。在第5天,解冻的A-LAK细胞的细胞毒性显着高于冷冻前的新鲜A-LAK(54.8%±10.2%对40.5%±6.4%)。与新鲜的对照细胞相比,冷冻的A-LAK细胞中淋巴细胞亚群的百分比没有明显变化。结论:PME可以简单地制备A-LAK细胞,并具有协同的抗肿瘤作用。 PA的组合。冷冻保存可以提高肝细胞癌患者A-LAK细胞的免疫活性。

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