首页> 外文期刊>Anticancer Research: International Journal of Cancer Research and Treatment >Ex vivo expansion of antitumor cytotoxic lymphocytes with tumor-associated antigen-loaded dendritic cells.
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Ex vivo expansion of antitumor cytotoxic lymphocytes with tumor-associated antigen-loaded dendritic cells.

机译:抗肿瘤细胞毒性淋巴细胞与肿瘤相关抗原加载的树突状细胞的离体扩增。

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摘要

Cell therapy with lymphocytes is an attractive approach for cancer immunotherapy. Methods to generate ex vivo effector cells directed against whole autologous tumor antigens are under investigation. Our procedure involved stimulation of autologous lymphocytes with antigen-pulsed dendritic cells (DC). Experimental conditions were established with DC, matured with TNFa, LPS and CD40L, from healthy donors and the M74 melanoma cell line. DC were pulsed with either irradiated, apoptotic or necrotic tumor cells or fused with tumor cells. Increase of lymphocyte cytotoxicity and IFNy production were repeatedly observed with tumor cell-loaded DC. Stimulation of tumor-associated antigen-specific lymphocytes was clearly shown. MelanA-MART1 (dominant melanoma-associated antigen) tetramer staining revealed a high frequency of specific T cells. Lymphocytes were able to efficiently lyse MelanA-MART1-pulsed T2 target and MelanA-expressing target cells (M74) after CD56+ cells depletion. We confirmed with other tumor cell lines that this DC-mediated procedure induced activation of cytolytic lymphocytes.
机译:用淋巴细胞进行细胞疗法是癌症免疫疗法的一种有吸引力的方法。正在研究产生针对整个自体肿瘤抗原的离体效应细胞的方法。我们的程序涉及用抗原脉冲树突状细胞(DC)刺激自体淋巴细胞。用来自健康供体和M74黑色素瘤细胞系的DC建立成熟的TNFa,LPS和CD40L的实验条件。用照射的,凋亡的或坏死的肿瘤细胞或与肿瘤细胞融合的脉冲DC。用载有肿瘤细胞的DC反复观察到淋巴细胞的细胞毒性和IFNγ产生的增加。清楚地显示出与肿瘤相关的抗原特异性淋巴细胞的刺激。 MelanA-MART1(主要与黑色素瘤相关的抗原)四聚体染色显示特异性T细胞的频率很高。 CD56 +细胞耗竭后,淋巴细胞能够有效裂解MelanA-MART1脉冲的T2靶标和表达MelanA的靶标细胞(M74)。我们用其他肿瘤细胞系证实了这种DC介导的过程诱导了溶细胞性淋巴细胞的激活。

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