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首页> 外文期刊>Human gene therapy >A Bicistronic Adenoviral Vector Carrying Cytosine Deaminase and Granulocyte-Macrophage Colony-Stimulating Factor Increases the Therapeutic Efficacy of Cancer Gene Therapy
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A Bicistronic Adenoviral Vector Carrying Cytosine Deaminase and Granulocyte-Macrophage Colony-Stimulating Factor Increases the Therapeutic Efficacy of Cancer Gene Therapy

机译:携带胞嘧啶脱氨酶和粒细胞 - 巨噬细胞殖民地刺激因子的双顺列腺病毒载体增加了癌症基因治疗的治疗效果

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摘要

The combination of cytotoxic treatment modalities, including oncolytic viral gene therapies and immunotherapy, usually yields a synergistic effect. In the current study, a bicistronic adenoviral vector, Ad-CD-GMCSF, carrying the cytosine deaminase (CD) and granulocyte-macrophage colony-stimulating factor (GM-CSF) transcription units driven by a cytomegalovirus promoter was constructed, and the in vitro efficacy of the vector was tested in tumor cell lines and a syngeneic mouse model of colon cancer. The tumor cells infected with Ad-CD-GMCSF vector were found to produce a substantial amount of GM-CSF in tumor cell lines. Accordingly, the vector carrying CD and GM-CSF transcription units together induced a potent antitumor immunity with a significantly increased number of tumor-specific T cells and tumor-specific T-cell cytotoxicity (p?
机译:细胞毒性治疗方式的组合,包括溶解病毒基因疗法和免疫疗法,通常产生协同效应。在目前的研究中,构建了由胞嘧啶脱蛋白酶(CD)和粒细胞 - 巨噬细胞群刺激因子(GM-CSF)转录的胞嘧啶腺嘌呤血管载体,患有胞嘧啶末端酶(CD)和粒细胞 - 巨噬细胞刺激单元的刺激单元,并体外载体的疗效在肿瘤细胞系和结肠癌的同联小鼠模型中测试。发现用Ad-CD-GMCSF载体感染的肿瘤细胞在肿瘤细胞系中产生大量的GM-CSF。因此,携带CD和GM-CSF转录单元的载体一起诱导有效的抗肿瘤免疫力,具有显着增加的肿瘤特异性T细胞和肿瘤特异性T细胞细胞毒性(P?<0.001)。与对照和仅携带CD转录单元的对照和腺病毒载体相比,Ad-CD-GMCSF处理小鼠的肿瘤生长速率显着降低(ad-CD;p≤0.05)。同样,AD-CD-GMCSF载体组的中位数总存活率显着高于对照和AD-CD组(34.0?±12.8〜14.0?±0.5和23.0?±2.8天; p?<?0.001)。总之,随着其细胞毒性效应,双顺逆型AD-CD-GMCSF载体的高免疫刺激作用具有优异的癌症潜力。

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