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重组牛型结核分枝杆菌卡介苗分泌人白细胞介素2

Secretion of human interleukin 2 by recombinant Mycobacterium bovis BCG.

作者信息

Kong D, Kunimoto D Y

机构信息

Department of Medical Microbiology and Infectious Diseases, University of Alberta, Edmonton, Canada.

出版信息

Infect Immun. 1995 Mar;63(3):799-803. doi: 10.1128/iai.63.3.799-803.1995.

Abstract

The human interleukin 2 (huIL-2) gene was introduced into Mycobacterium bovis BCG by using the integrative vector pMV306. To express and secrete huIL-2 from BCG, two different plasmids, CI and CII, were made. In CI, the huIL-2-encoding region was under the control of the alpha-antigen promoter of BCG; in CII, the expression of huIL-2 was regulated by the heat shock protein 60 promoter. A signal peptide sequence isolated from the naturally secreted alpha-antigen of BCG was inserted between the promoter and huIL-2-encoding region to facilitate secretion. Both huIL-2 expression plasmids were integrated into the BCG genome when introduced into the BCG Pasteur strain by electroporation. Approximately 150 U of huIL-2 was secreted into the medium of a BCG-CII culture, while the BCG-CI cells secreted approximately one-sixth of that amount. When the IL-2-expressing BCG strain BCG-CII was injected intravenously into BALB/c mice, the number of BCG cells in the spleens of these mice was significantly less than the number in the control mice. The decreased number of IL-2-expressing BCG cells is likely due to the augmentation of the host immune response by the secreted huIL-2, although the exact mechanism is not known.

摘要

通过使用整合载体pMV306,将人白细胞介素2(huIL-2)基因导入牛分枝杆菌卡介苗(Mycobacterium bovis BCG)。为了使卡介苗表达并分泌huIL-2,构建了两种不同的质粒,即CI和CII。在CI中,huIL-2编码区受卡介苗α抗原启动子的控制;在CII中,huIL-2的表达由热休克蛋白60启动子调控。在启动子和huIL-2编码区之间插入了一个从卡介苗天然分泌的α抗原中分离出的信号肽序列,以促进分泌。当通过电穿孔将这两种huIL-2表达质粒导入卡介苗巴斯德菌株时,它们都整合到了卡介苗基因组中。在卡介苗-CII培养物的培养基中分泌了约150 U的huIL-2,而卡介苗-CI细胞分泌的量约为其六分之一。当将表达IL-2的卡介苗菌株BCG-CII静脉注射到BALB/c小鼠体内时,这些小鼠脾脏中的卡介苗细胞数量明显少于对照小鼠。表达IL-2的卡介苗细胞数量减少可能是由于分泌的huIL-2增强了宿主免疫反应,尽管确切机制尚不清楚。

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