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CTL Induction Using Cultured Dendritic Cells and Ibmor-RNA in Gastric Cancer

机译:CTL在胃癌中使用培养的树突细胞和IBMOR-RNA诱导

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CTL induction using cultured dendritic cells (DCs) and tumor-RNA derived from gastric cancer (GC) was studied. DCs were generated from an adherent fraction of peripheral blood mononuclear cells (PBMCs) in the presence of GM-CSF and IL-4. mRNA was purified from a GC cell line or caner cells from GC patients, and subjected to in vitro TV-amplification. DCs were electroporated with amplified RNA and used for stimulating PBMCs to generate tumor RNA-introduced DC-activated killer (TRiDAK) cells. Tumor RNA-introduced DCs (RNA/DCs), but not normal cell-derived RNA/DCs, could stimulate lymphocytes. TRiDAK cells showed IFN-gamma spots and killing activity against tumor cells, but not against normal cells. TRiDAK activity was observed in an RNA-specific manner. TRiDAK response against tumor cells was abrogated with anti-class I or -class II antibodies, or with anti-TCR antibody. These results suggest that TRiDAK cell generation is feasible and active in patients with GC.
机译:研究了使用培养的树突细胞(DC)和来自胃癌(GC)的肿瘤-RNA的CTL诱导。在GM-CSF和IL-4存在下,从外周血单核细胞(PBMC)的粘附部分产生DC。从GC患者的GC细胞系或Caner细胞中纯化mRNA,并进行体外电视扩增。用扩增的RNA电穿过DC,并用于刺激PBMC以产生肿瘤RNA引入的直流激活杀伤(Tridak)细胞。肿瘤RNA引入的DCS(RNA / DCS),但不是正常的细胞衍生的RNA / DCS,可以刺激淋巴细胞。 Tridak细胞显示IFN-Gamma斑点和针对肿瘤细胞的杀死活性,但不抗逆正常细胞。以RNA特异性方式观察Tridak活性。用抗级I或-Class II抗体或抗TCR抗体脱氮针对肿瘤细胞的曲线响应。这些结果表明,在GC的患者中,Tridak细胞生成是可行和活跃的。

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