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[大鼠实验性脑肿瘤的过继免疫治疗——LAK细胞的诱导及其生物学特性]

[Adoptive immunotherapy in experimental brain tumor in rats--induction of LAK cells and their biological characteristic].

作者信息

Takai N, Tanaka R, Yoshida S, Hara N, Saito T

机构信息

Department of Neurosurgery, Niigata University, Japan.

出版信息

No To Shinkei. 1987 Sep;39(9):879-84.

PMID:3500734
Abstract

We have investigated the biological characteristic of Lymphokine Activated Killer (LAK) cells induced from spleen cells (SPC) of Fischer rats. Supernatant of 48 hour culture medium (RPMI-1640, 10% FBS, 2-ME: 5 X 10(-5) M, HEPES: 10 mM) of SPC (1 X 10(6)/ml) from Wistar rats in the presence of Con A (5 micrograms/ml) was used as Interleukin 2 (IL-2). LAK cells were generated by co-cultivation of SPC (4 X 10(6)/ml) from Fischer rats with peak reactivity on the 2 nd or 3 rd day of culture. Lytic activity was observed against not only syngeneic tumor cells (T9, RSV induced brain tumor), but also allogenic (KMT-17) and xenogenic (K 562, Raji cell, G 361, YAC-1) tumor cells, while no lytic activity was observed against normal brain cells. Cell depletion test, dye exclution test and immunofluorescence method using monoclonal Antibodies (mAbs) revealed that LAK cells partially belonged to the population of activated T cell group (W 3/13, OX 4 positive) but the precursor cells did not react with any mAbs used (W 3/13, W 3/25, OX 4, OX 8). On the basis of these results, more effective and useful administration of LAK cells is now under investigations by using the rats with brain tumors.

摘要

我们研究了从Fischer大鼠脾细胞(SPC)诱导产生的淋巴因子激活杀伤细胞(LAK细胞)的生物学特性。来自Wistar大鼠的SPC(1×10⁶/ml)在伴刀豆球蛋白A(Con A,5微克/毫升)存在的情况下,48小时培养基(RPMI - 1640,10%胎牛血清,2 - 巯基乙醇:5×10⁻⁵M,羟乙基哌嗪乙磺酸:10毫摩尔)的上清液被用作白细胞介素2(IL - 2)。LAK细胞通过将培养第2天或第3天反应峰值时的Fischer大鼠的SPC(4×10⁶/ml)共同培养产生。观察到其不仅对同基因肿瘤细胞(T9,劳氏肉瘤病毒诱导的脑肿瘤)有杀伤活性,而且对异基因(KMT - 17)和异种(K562、Raji细胞、G361、YAC - 1)肿瘤细胞也有杀伤活性,而对正常脑细胞无杀伤活性。细胞清除试验、染料排除试验以及使用单克隆抗体(mAb)的免疫荧光法显示,LAK细胞部分属于活化T细胞群体(W3/13、OX4阳性),但其前体细胞不与所使用的任何mAb(W3/13、W3/25、OX4、OX8)发生反应。基于这些结果,目前正在利用患脑肿瘤的大鼠研究LAK细胞更有效和有用的给药方法。

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