首页> 外文期刊>Cellular immunology >Killing effect of interleukin-13 receptor alpha 2 (IL-13Ralpha2) sensitized DC-CTL cells on human glioblastoma U251 cells.
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Killing effect of interleukin-13 receptor alpha 2 (IL-13Ralpha2) sensitized DC-CTL cells on human glioblastoma U251 cells.

机译:白细胞介素13受体α2(IL-13Ralpha2)致敏的DC-CTL细胞对人胶质母细胞瘤U251细胞的杀伤作用。

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Recent studies show that IL-13Ralpha2, a brain tumor-associated antigen for IL-13, may play a role in immunotherapy for glioblastoma. Thus, we stimulated the lymphocyte by monocyte-derived dendritic cells (DCs). The DCs were pulsed with IL-13Ralpha2 in vitro and then co-cultured with lymphocytes. After inducing cytotoxic T cells (CTLs) and co-culturing with U251 cells for 24 h in 96 wells, Cell Count Kit-8 (CCK-8) was added to every well equally. The optical density (OD) value was detected and recorded after 2 h. The DCs efficiently presented the antigen to the CTLs, resulting in CTLs activation and proliferation. The induced CTLs showed specific cytotoxic against U251 cells (P<0.01). The results demonstrated that IL-13Ralpha2 induced CTLs could kill glioma U251 in vitro, which suggests that IL-13 Ralpha2 might have such an impact in vivo and thus recombinant IL-13Ra2 protein might be used as an anti-tumor vaccine, providing a promising new strategy for the treatment of brain malignant gliomas.
机译:最近的研究表明,IL-13Ralpha2,一种与脑瘤相关的IL-13抗原,可能在胶质母细胞瘤的免疫治疗中发挥作用。因此,我们通过单核细胞衍生的树突状细胞(DCs)刺激了淋巴细胞。将DC用IL-13Ralpha2体外脉冲,然后与淋巴细胞共培养。诱导细胞毒性T细胞(CTL)并与U251细胞在96孔中共培养24小时后,将Cell Count Kit-8(CCK-8)平均添加到每个孔中。 2小时后检测并记录光密度(OD)值。 DC有效地将抗原呈递给CTL,导致CTL活化和增殖。诱导的CTLs表现出对U251细胞的特异性细胞毒性(P <0.01)。结果表明IL-13Ralpha2诱导的CTLs可以在体外杀死神经胶质瘤U251,这表明IL-13 Ralpha2可能在体内具有这种作用,因此重组IL-13Ra2蛋白可以用作抗肿瘤疫苗,提供了有希望的治疗脑恶性神经胶质瘤的新策略。

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