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中国防痨杂志 ›› 2013, Vol. 35 ›› Issue (9): 643-648.

• 论著 • 上一篇    下一篇

结核分枝杆菌融合抗原38F和64F诊断活动性肺结核的价值

郄霜 张立 戴振华 赵平 杨锡琴 郭兰芹 修冰水 陈堃 王国华 张贺秋 冯晓燕   

  1. 100085  北京,军事医学科学院基础医学研究所 生物诊断研究室[郄霜(研究生,现在063000 唐山,河北联合大学免疫学教研室)、戴振华、杨锡琴、修冰水、陈堃、王国华、张贺秋、冯晓燕];天津海河医院检验科(张立);北京市朝阳区疾病预防控制中心检验科(赵平);华北石油总医院社区卫生服务中心(郭兰芹)
  • 收稿日期:2013-06-09 出版日期:2013-09-10 发布日期:2013-09-08
  • 通信作者: 冯晓燕 E-mail:xyfeng2002@126.com
  • 基金资助:

    国家自然科学基金(30772067);“十一五”国家科技重大专项(2009ZX10004-718)

The value of Mycobacterium tuberculosis fusion antigen 38F and 64F in the diagnosis of active tuberculosis

QIE Shuang,ZHANG Li, DAI Zhen-hua,ZHAO Ping,YANG Xi-qin,GUO Lan-qin,XIU Bing-shui, CHEN Kun, WANG Guo-hua, ZHANG He-qiu, FENG Xiao-yan   

  1. Biological Diagnostic Laboratory,Institute of Basic Medical Sciences, Academy of Military Medical Sciences, Beijing 100085, China (Master Degree Candidate,Now in: Department of Immunology,Hebei United University,Tangshan 063000,China)
  • Received:2013-06-09 Online:2013-09-10 Published:2013-09-08
  • Contact: FENG Xiao-yan E-mail:xyfeng2002@126.com

摘要: 目的  探讨结核分枝杆菌融合抗原38F和64F对活动性肺结核患者血清中IgG、IgM和IgA抗体检测的诊断价值。 方法  利用结核分枝杆菌抗原优势肽段融合抗原38F和64F,通过ELISA法对223例活动性肺结核患者进行结核分枝杆菌特异性IgG、IgM和IgA抗体水平检测。223例活动性肺结核患者分为三组,第一组为涂片和培养共同阳性组(86例),第二组为涂片阴性且培养阳性组(51例),第三组为涂片和培养共同阴性组(86例)。 结果 223例活动性肺结核病患者,第一组IgG、IgM和IgA的联合检出率为79.07%(68/86);第二组IgG、IgM和IgA的联合检出率为62.75%(32/51);第三组IgG、IgM和IgA的联合检出率为69.77%(60/86)。全部样本血清学方法的检出率为71.75%(160/223)。结论  结核分枝杆菌融合抗原38F和64F对于活动性肺结核具有较高的辅助诊断价值,并且IgG、IgM和IgA抗体联合检测可以提高检出率。

关键词: 结核, 肺/诊断, 抗体, 细菌, 细菌蛋白质类, 血清学试验

Abstract: Objective To explore the diagnostic value of Mycobacterium tuberculosis fusion antigen 38F and 64F in detecting IgG, IgM and IgA antibody in serum of patients with active pulmonary tuberculosis. Methods By using enzyme-linked immuno sorbent assay (ELISA) method, IgG, IgM and IgA antibody levels in serum of 223 patients with active pulmonary tuberculosis were detected with the Mycobacterium tuberculosis seven immune-dominat peptide fusion antigen 38F and 64F. Patients with active pulmonary tuberculosis were divided into three groups. The first group was co-positive cases of smear and culture examination (n=86). The second group was smear-negative and culture-positive (n=51). The third group was co-negative cases of smear and culture examination (n=86). Results The joint detection rate of IgG, IgM and IgA was 79.07% (68/86) for the first group, 62.75% (32/51) for the second group and 69.77% (60/86) for the third group. The detection rate of all samples by serological method was 71.75% (160/223). Conclusion Mycobacterium tuberculosis fusion antigen 38F and 64F have high assistant diagnostic values to active pulmonary tuberculosis, and the detection rate is increased significantly through joint detection of IgG, IgM and IgA antibody.

Key words: Tuberculosis, pulmonary/diagnosis, Antibodies, bacterial, Bacterial protein, Serologic tests