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采用肿瘤特异性细胞毒性T淋巴细胞克隆对小鼠恶性胶质瘤进行特异性过继性免疫治疗。

Specific adoptive immunotherapy with tumor-specific cytotoxic T-lymphocyte clone for murine malignant gliomas.

作者信息

Yamasaki T, Handa H, Yamashita J, Watanabe Y, Namba Y, Hanaoka M

出版信息

Cancer Res. 1984 May;44(5):1776-83.

PMID:6608988
Abstract

The efficacy of glioma-specific cytotoxic T-lymphocyte for a syngeneic murine malignant glioma (a 20-methylcholanthrene-induced ependymoblastoma, 203-glioma) was investigated. The cytotoxic clone (G-CTLL 1), established and expanded exponentially by T-cell growth factor, has retained target specificity for more than 6 months. In adoptive therapy and Winn assay, the in vivo antitumor activity of G-CTLL 1 was demonstrated against mice inoculated intracranially with 203-glioma cells. The therapeutic effects in adoptive immunotherapy were largely dependent on dose and time of i.v. administration, although the therapy was rather ineffective in condition of increased intracranial pressure due to the tumor growth. The mechanisms responsible for the in vivo protection were probably related to the killing activity of G-CTLL 1 or the tumor-specific production of immune interferon by G-CTLL 1.

摘要

研究了胶质瘤特异性细胞毒性T淋巴细胞对同基因小鼠恶性胶质瘤(一种20-甲基胆蒽诱导的室管膜母细胞瘤,203-胶质瘤)的疗效。通过T细胞生长因子建立并呈指数扩增的细胞毒性克隆(G-CTLL 1),已保持靶标特异性超过6个月。在过继性治疗和Winn试验中,证明G-CTLL 1对颅内接种203-胶质瘤细胞的小鼠具有体内抗肿瘤活性。过继性免疫治疗的疗效在很大程度上取决于静脉注射给药的剂量和时间,尽管在肿瘤生长导致颅内压升高的情况下该治疗效果不佳。体内保护的机制可能与G-CTLL 1的杀伤活性或G-CTLL 1产生肿瘤特异性免疫干扰素有关。

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