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首页> 外文期刊>Genetics and Molecular Research >Enhancement of dendritic cells with melanoma-associated antigen 3 for inducing cytotoxicity by cytotoxic T lymphocytes on bladder cancer BIU-87 cells
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Enhancement of dendritic cells with melanoma-associated antigen 3 for inducing cytotoxicity by cytotoxic T lymphocytes on bladder cancer BIU-87 cells

机译:黑色素瘤相关抗原3增强树突状细胞,以通过细胞毒性T淋巴细胞诱导膀胱癌BIU-87细胞发生细胞毒性

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To determine the cytotoxic effect of lymphocytes activated by melanoma-associated antigen 3 (MAGE-3)-sensitized dendritic cells (DCs) on BIU-87 tumor cells, and to evaluate the possibility of MAGE-3-peptide-pulsed DCs as a vaccine in bladder cancer immunotherapy, the proliferation of T cells and the activity of cytotoxic T lymphocytes (CTLs) were examined by the MTT method. CTLs were induced by MAGE-3-sensitized DCs, or by ovalbumin (OVA) peptide and non-sensitized DCs as controls, respectively. The results indicated that MAGE-3-sensitized DCs have the ability to promote the proliferation of T cells as well as the cytotoxic activity of CTLs on bladder cancer cells in comparison with OVA peptide and non-sensitized DCs. In other words, DCs sensitized by the MAGE-3 antigen peptide could obviously upregulate the proliferation of T cells, which resulted in the growth inhibition of bladder cancer BIU-87 cells. In addition, MAGE-3-sensitized DCs played an important role in inhibiting the growth of human BIU-87 tumor xenografts in nude mice.
机译:确定由黑色素瘤相关抗原3(MAGE-3)致敏的树突状细胞(DC)激活的淋巴细胞对BIU-87肿瘤细胞的细胞毒作用,并评估MAGE-3肽脉冲DC作为疫苗的可能性在膀胱癌免疫疗法中,MTT法检测了T细胞的增殖和细胞毒性T淋巴细胞(CTL)的活性。 CTL由MAGE-3致敏的DC诱导,或由卵清蛋白(OVA)肽和非致敏的DC诱导作为对照。结果表明,与OVA肽和未敏化的DC相比,MAGE-3敏化的DC具有促进T细胞增殖以及CTL对膀胱癌细胞的细胞毒活性的能力。换句话说,MAGE-3抗原肽致敏的DCs明显上调T细胞的增殖,从而导致膀胱癌BIU-87细胞的生长受到抑制。此外,MAGE-3敏感的DC在抑制裸鼠中人BIU-87肿瘤异种移植的生长中起着重要作用。

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