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[肿瘤坏死因子-α基因转染的淋巴因子激活的杀伤细胞对人胶质瘤细胞的增强抗肿瘤作用]

[Enhanced anti-tumor effect of lymphokine-activated killer cells transfected with tumor necrosis factor-alpha gene on human glioma cells].

作者信息

Tashiro T

机构信息

Department of Neurosurgery, Hokkaido University School of Medicine, Sapporo, Japan.

出版信息

Hokkaido Igaku Zasshi. 1994 Jul;69(4):742-9.

PMID:7959591
Abstract

Tumor necrosis factor (TNF)-alpha gene were transfected into lymphokine-activated killer (LAK) cells generated from peripheral blood lymphocytes incubated with recombinant interleukin-2 by means of novel liposomes with a positive charge on their surface. The cells secreted significant amounts of TNF-alpha into the culture medium and exhibited reinforcement of cytotoxicity toward a human glioma cell line (U251-SP), being three times more cytotoxic than nontransfected LAK cells. The mechanism for the reinforcement of cytotoxicity is considered to involve not only an increase in TNF-alpha secretion from LAK cells but also its expression on their surface. Intratumoral or intrathecal injection of LAK cells transfected with the TNF-alpha gene may be useful for the treatment of patients with malignant glioma.

摘要

通过表面带正电荷的新型脂质体,将肿瘤坏死因子(TNF)-α基因转染到由外周血淋巴细胞与重组白细胞介素-2孵育产生的淋巴因子激活的杀伤细胞(LAK细胞)中。这些细胞向培养基中分泌大量的TNF-α,并对人胶质瘤细胞系(U251-SP)表现出细胞毒性增强,其细胞毒性是非转染LAK细胞的三倍。细胞毒性增强的机制被认为不仅涉及LAK细胞TNF-α分泌的增加,还涉及其在细胞表面的表达。瘤内或鞘内注射转染了TNF-α基因的LAK细胞可能对恶性胶质瘤患者的治疗有用。

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