首页> 外文期刊>Japanese Journal of Cancer Research >Successful induction of tumor-specific cytotoxic T lymphocytes from patients with non-small cell lung cancer using CD80-transfected autologous tumor cells.
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Successful induction of tumor-specific cytotoxic T lymphocytes from patients with non-small cell lung cancer using CD80-transfected autologous tumor cells.

机译:使用CD80转染的自体肿瘤细胞成功诱导非小细胞肺癌患者的肿瘤特异性细胞毒性T淋巴细胞。

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Cytotoxic T lymphocytes (CTL) against human lung cancer cells are difficult to induce by a conventional method using tumor cell stimulation probably due to an insufficiency of tumor antigens (TA) or costimulatory molecules such as CD80. We, therefore, investigated the potential of CD80-transfected tumor cells as stimulators of the in vitro induction of autologous tumor-specific CTL from regional lymph node lymphocytes in patients with lung cancer. Five non-small cell lung cancer cell lines (two adenocarcinomas, 1 squamous cell carcinoma, 1 large cell carcinoma and 1 adenosquamous cell carcinoma) were established from surgical specimens and were successfully transduced with a plasmid constructed with expression vector pBj and human CD80 cDNA, using a lipofection method. CD80-transfected tumor cells (CD80-AT) significantly augmented the proliferation of autologous lymphocytes from all cases as compared with non-transfected tumor cells (AT). AT-stimulated lymphocytes from 4 out of 5 cases did not show any cytotoxicity against AT; however, lymphocytes stimulated with CD80-AT exhibited substantial cytotoxicity against parental AT in all 5 cases tested. AT-stimulated lymphocytes derived from only one out of 5 cases showed major histocompatibility complex (MHC)-class I-restricted cytokine production in response to AT, while the MHC-class I-restricted responses were found in CD80-AT-stimulated lymphocytes from 4 out of 5 cases. These results indicate that CD80 on tumor cells could be a beneficial costimulatory molecule to elicit CTL against lung cancer, and also show that TA recognized by CTL was frequently expressed on lung cancer cells.
机译:通过使用肿瘤细胞刺激的常规方法难以诱导针对人肺癌细胞的细胞毒性T淋巴细胞(CTL),这可能是由于肿瘤抗原(TA)或诸如CD80之类的共刺激分子不足所致。因此,我们研究了CD80转染的肿瘤细胞作为从肺癌患者的区域淋巴结淋巴细胞体外诱导自体肿瘤特异性CTL的刺激物的潜力。从手术标本中建立了五个非小细胞肺癌细胞系(两个腺癌,1个鳞状细胞癌,1个大细胞癌和1个腺鳞癌),并成功地用表达载体pBj和人CD80 cDNA构建的质粒进行了转导,使用脂质转染法。与未转染的肿瘤细胞(AT)相比,CD80转染的肿瘤细胞(CD80-AT)显着增强了所有病例的自体淋巴细胞的增殖。 5例患者中有4例受AT刺激的淋巴细胞未表现出对AT的任何细胞毒性。然而,用CD80-AT刺激的淋巴细胞在所有5例受测病例中均表现出对亲本AT的实质性细胞毒性。 5例中只有1例受AT刺激的淋巴细胞表现出对AT的主要组织相容性复合物(MHC)I类限制性细胞因子生成,而CD80-AT刺激的淋巴细胞中MHC I类限制性应答被发现。 5例中有4例。这些结果表明,肿瘤细胞上的CD80可能是引发CTL对抗肺癌的有益共刺激分子,并且还表明CTL识别的TA经常在肺癌细胞上表达。

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