首页 | 本学科首页   官方微博 | 高级检索  
     

结核分枝杆菌38-KDa抗原酶联免疫测定结核抗体的方法建立
引用本文:胡忠义,郭春祥,许成文,李建林. 结核分枝杆菌38-KDa抗原酶联免疫测定结核抗体的方法建立[J]. 上海预防医学, 1998, 0(10)
作者姓名:胡忠义  郭春祥  许成文  李建林
作者单位:上海市结核病防治中心!200031(胡忠义,许成文),上海晶莹生物技术公司(郭春祥,李建林)
摘    要:目的:建立检测结核抗体的酶联免疫吸附试验,并探讨方法的最佳测定条件。方法:采用结核分枝杆菌38—KDa基因重组抗原包被固相载体进行酶联免疫测定。结果:170份血清结核抗体测定,敏感性为74.0%,特异性为95.7%;Omega试剂的敏感性为68.0%,特异性为97.1%。两种38-KDa重组抗原的测定结果差异无显著性(P>0.05)。结论:38一KDa。抗原性能达到或接近Omega产品.本法灵敏、特异,可作为结核病的辅助诊断方法之一。

关 键 词:抗原  结核分枝杆菌  基因工程  免疫测定  抗体

Establishment of enzyme-immunoassay for the detection of tubercle antibodies with 38 - KDa antigen ofM. tuberculosis
Hu Zhongyi. Establishment of enzyme-immunoassay for the detection of tubercle antibodies with 38 - KDa antigen ofM. tuberculosis[J]. Shanghai Journal of Preventive Medicine, 1998, 0(10)
Authors:Hu Zhongyi
Abstract:0bjective: Establish enzyme - immunoassay for the detection of tubercle antibodies and describeits optimal conditions. Methods:With recombinant 38 - KDa antigen of M. tuberculosis coating soid carrier.Results: The sensitivity and specificity of this method was 74. O % and 95. 7 %, while the Omega reagent was68. 0 % and 97. 1 % respectively by detection of l70 sera samples. There was no significantly differences in re-suIts by two reagents (P >0. O5). Conclusion: According to its sensitity and specificity value, this method canserve as supplementary method f0r the diagnosis of tuberculosis.
Keywords:Antigen  Mycobacterium tuberculosis  Genetic engineering  Immunoassay  Antibody
本文献已被 CNKI 等数据库收录!
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