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用牛分枝杆菌卡介苗的脱氧核糖核酸组分体外增强自然杀伤细胞活性及α/β干扰素和γ干扰素的产生。

In vitro augmentation of natural killer cell activity and production of interferon-alpha/beta and -gamma with deoxyribonucleic acid fraction from Mycobacterium bovis BCG.

作者信息

Yamamoto S, Kuramoto E, Shimada S, Tokunaga T

机构信息

Department of Cellular Immunology, National Institute of Health, Tokyo.

出版信息

Jpn J Cancer Res. 1988 Jul;79(7):866-73. doi: 10.1111/j.1349-7006.1988.tb00049.x.

DOI:10.1111/j.1349-7006.1988.tb00049.x
PMID:2459094
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5917587/
Abstract

A nucleic acid-rich fraction extracted and purified from BCG (MY-1) augmented natural killer (NK) cell activity of mouse spleen cells in vitro, and produced factor(s) which showed anti-viral activity and rendered normal macrophages cytotoxic towards tumor cells. These cellular responses were induced by the MY-1 digested preliminarily with RNase, but not by the MY-1 digested with DNase, indicating that DNA contained in MY-1 was essential for the responses. The function of the factor to activate macrophages was destroyed by treatment with a small amount of anti-interferon (IFN)-gamma antiserum or under acidic conditions (pH 2), but not by treatment with anti-IFN-alpha/beta antiserum, while the anti-viral activity was destroyed almost completely by treatment with anti-IFN-alpha/beta antiserum. It appears that DNA from BCG stimulated mouse spleen cells in vitro, resulting in augmentation of NK activity and production of IFN-alpha/beta and -gamma.

摘要

从卡介苗(MY-1)中提取并纯化的富含核酸的组分,在体外增强了小鼠脾细胞的自然杀伤(NK)细胞活性,并产生了具有抗病毒活性的因子,使正常巨噬细胞对肿瘤细胞具有细胞毒性。这些细胞反应是由先用核糖核酸酶预处理的MY-1诱导的,而不是由用脱氧核糖核酸酶处理的MY-1诱导的,这表明MY-1中所含的DNA对这些反应至关重要。该因子激活巨噬细胞的功能在用少量抗干扰素(IFN)-γ抗血清处理或在酸性条件(pH 2)下被破坏,但用抗IFN-α/β抗血清处理则不会,而抗病毒活性在用抗IFN-α/β抗血清处理后几乎完全被破坏。似乎卡介苗的DNA在体外刺激小鼠脾细胞,导致NK活性增强以及IFN-α/β和 -γ的产生。

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Jpn J Cancer Res. 1986 Aug;77(8):808-16.