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体外和体内药物对细胞介导的细胞毒性作用的比较研究。

Comparative study of in vitro and in vivo drug effects on cell-mediated cytotoxicity.

作者信息

Borel J F

出版信息

Immunology. 1976 Oct;31(4):631-41.

PMID:824198
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1445361/
Abstract

Cell-mediated cytolysis (CMC) was assayed in a system using spleen cells from mice (C57BL/6) sensitized with allogeneic tumour cells (DBA/2 mastocytoma P-815). Anti-inflammatory drugs, immunosuppressives, inhibitors of cell division and other agents were investigated for their capacity to inhibit CMC in three different ways. First, inhibition of CMC after in vitro addition of drug was observed with corticosteroids, some immunosuppressives and inhibitors of cell division. Secondly, suppression of CMC after a single drug administration to sensitized mice shortly before being killed was found with corticosteroids, several immunosuppressives and irradiation. Thirdly, prevention of development of CMC by repeated drug treatment (immunosuppressive schedule) was achieved with most immunosuppressives and cytostatic drugs. Non-steroidal anti-inflammatory drugs were inactive in these tests. Correlation of effects between the three procedures was very poor and it is suggested that various mechanisms may be involved in the different assays.

摘要

在一个系统中检测细胞介导的细胞溶解作用(CMC),该系统使用用同种异体肿瘤细胞(DBA/2肥大细胞瘤P-815)致敏的小鼠(C57BL/6)的脾细胞。研究了抗炎药、免疫抑制剂、细胞分裂抑制剂和其他药物以三种不同方式抑制CMC的能力。首先,观察到皮质类固醇、一些免疫抑制剂和细胞分裂抑制剂在体外添加药物后对CMC有抑制作用。其次,在用皮质类固醇、几种免疫抑制剂和辐射处理致敏小鼠后,在处死前不久单次给药可抑制CMC。第三,大多数免疫抑制剂和细胞抑制药物通过重复药物治疗(免疫抑制方案)可预防CMC的发展。非甾体抗炎药在这些试验中无活性。这三种方法之间的效应相关性很差,提示不同的检测方法可能涉及多种机制。

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本文引用的文献

1
Studies on the mechanism of the cytolytic effect of sensitized lymphocytes.致敏淋巴细胞细胞溶解作用机制的研究。
J Immunol. 1966 Jan;96(1):80-4.
2
Lymphocyte in vitro cytotoxicity: mechanisms of immune and non-immune small lymphocyte mediated target L cell destruction.淋巴细胞体外细胞毒性:免疫和非免疫性小淋巴细胞介导的靶L细胞破坏机制。
J Immunol. 1968 Jul;101(1):111-20.
3
Glucocorticoids and cellular immunity in vitro. Facilitation of the sensitization phase and inhibition of the effector phase of a lymphocyte anti-fibroblast reaction.糖皮质激素与体外细胞免疫。淋巴细胞抗成纤维细胞反应致敏阶段的促进作用及效应阶段的抑制作用。
J Exp Med. 1970 Dec 1;132(6):1055-70. doi: 10.1084/jem.132.6.1055.
4
Properties of colchicine binding protein from chick embryo brain. Interactions with vinca alkaloids and podophyllotoxin.鸡胚脑秋水仙碱结合蛋白的特性。与长春花生物碱和鬼臼毒素的相互作用。
Biochemistry. 1970 Dec 8;9(25):4999-5007. doi: 10.1021/bi00827a026.
5
Studies of allograft immunity in mice. II. Mechanism of target cell inactivation in vitro by sensitized lymphocytes.小鼠同种异体移植免疫研究。II. 致敏淋巴细胞在体外使靶细胞失活的机制。
Immunology. 1970 Apr;18(4):517-35.
6
Studies of allograft immunity in mice. I. Induction, development and in vitro assay of cellular immunity.小鼠同种异体移植免疫研究。I. 细胞免疫的诱导、发展及体外检测
Immunology. 1970 Apr;18(4):501-15.
7
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Immunology. 1968 Feb;14(2):181-96.
8
Inhibition of the lymphocyte-mediated cytotoxic reaction by anti-inflammatory drugs.抗炎药物对淋巴细胞介导的细胞毒性反应的抑制作用。
J Reticuloendothel Soc. 1974 Feb;15(2):112-7.
9
Evaluation of the effects of cytochalasin B on lymphocyte-mediated cytolysis.细胞松弛素B对淋巴细胞介导的细胞溶解作用的评估。
Transplantation. 1973 Dec;16(6):684-6. doi: 10.1097/00007890-197312000-00027.
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Schedule dependency of the antileukemic activity of the podophyllotoxin-derivative VP 16-213 (NSC-141540) in L1210 leukemia.鬼臼毒素衍生物VP 16 - 213(NSC - 141540)对L1210白血病抗白血病活性的时间依赖性
Acta Pathol Microbiol Scand A. 1973 Sep;81(5):715-24. doi: 10.1111/j.1699-0463.1973.tb03564.x.