首页 | 本学科首页   官方微博 | 高级检索  
     检索      

表达HBHA和hIL-12融合蛋白的重组耻垢分枝杆菌对结核分枝杆菌感染小鼠的免疫治疗作用
引用本文:赵善民,师长宏.表达HBHA和hIL-12融合蛋白的重组耻垢分枝杆菌对结核分枝杆菌感染小鼠的免疫治疗作用[J].科学技术与工程,2012,12(2):415-417.
作者姓名:赵善民  师长宏
作者单位:1. 第四军医大学实验动物中心,西安,710032
2. 第四军医大学微生物学教研室,西安,710032
基金项目:国家"863"专项课题,国家自然科学基金,陕西省自然科学基金
摘    要:评价表达HBHA和hIL12融合蛋白的重组耻垢分枝杆菌用于结核分枝杆菌感染小鼠的免疫治疗效果.结核分枝杆菌H37Rv感染小鼠4周后,用表达HBHA和hIL12融合蛋白的重组耻垢分枝杆菌免疫治疗,检测免疫小鼠肺部荷菌量和组织病理变化.重组耻垢分枝杆菌可有效控制感染小鼠肺部结核分枝杆菌的荷菌量,减轻病理损伤.但在降低肺部荷菌量方面不如化疗药物.表达HBHA和hIL12融合蛋白的重组耻垢分枝杆菌可有效控制结核分枝杆菌在小鼠体内的增殖,可能成为联合化疗药物控制结核病的有效候选疫苗.

关 键 词:重组耻垢分枝杆菌  结核分枝杆菌  HBHA  hIL-12
收稿时间:2011/10/31 0:00:00
修稿时间:2011/11/8 0:00:00

Therapeutic efficacy of a recombinant Mycobacterium smegmatis expressing an HBHA and hIL12 fusion protein against Mycobacterium tuberculosis infection induced in mice
zhaoshanmin and shichanghong.Therapeutic efficacy of a recombinant Mycobacterium smegmatis expressing an HBHA and hIL12 fusion protein against Mycobacterium tuberculosis infection induced in mice[J].Science Technology and Engineering,2012,12(2):415-417.
Authors:zhaoshanmin and shichanghong
Institution:2 (Laboratory Animals Center1,Department of Microbiology2,Fourth Military Medical University,Xi’an 710032,P.R.China)
Abstract:We tried to investigate whether the HBHA-hIL12-rMS constructed could be effective as treatment against established infection. Mice were infected with the H37Rv strain via the tail vein. Four weeks after infection, the mice were were treated with HBHA-hIL12-rMS. Determination of bacterial burden and histopathology were performed at 8 weeks post-infection. The HBHA-hIL12-rMS decreased lung bacterial load in lungs and reduced lung damage compared to the saline, although cannot achieve therapeutic drug levels. The HBHA-hIL12-rMS could be effective as treatment against established infection. It may be a useful vaccine candidate combined treatment with the therapeutic drugs.
Keywords:Recombinant M  smegmatis  M  tuberculosis  HBHA  hIL-12
本文献已被 CNKI 万方数据 等数据库收录!
点击此处可从《科学技术与工程》浏览原始摘要信息
点击此处可从《科学技术与工程》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号