Weldingh Karin, Rosenkrands Ida, Okkels Limei Meng, Doherty T Mark, Andersen Peter
Department of Infectious Disease Immunology, Statens Serum Institut, Artillerivej 5, DK-2300 Copenhagen S, Denmark.
J Clin Microbiol. 2005 Jan;43(1):57-65. doi: 10.1128/JCM.43.1.57-65.2005.
Improved diagnostic reagents are needed for the detection of Mycobacterium tuberculosis infections, and the development of a serodiagnostic test would complement presently available diagnostic methods. The aim of the present study was to identify novel serological targets for use for the future serodiagnosis of tuberculosis (TB). We cloned and expressed 35 M. tuberculosis proteins as recombinant proteins in Escherichia coli and analyzed their serodiagnostic potentials. By a two-step selection process, four superior seroantigens, TB9.7, TB15.3, TB16.3, and TB51, were identified, none of which has been described before. The four novel antigens were tested with panels of sera from smear-positive and smear-negative TB patients from areas both where TB is endemic and where TB is not endemic, with recognition frequencies ranging from 31 to 93% and with a specificity of at least 97%. The single most potent antigen was TB16.3, which had a sensitivity of 48 to 55% with samples from Danish resident TB patients and a sensitivity of 88 to 98% with samples from African TB patients. Importantly, the TB16.3 and the TB9.7 antigens were recognized by more than 85% of the samples from TB patients coinfected with human immunodeficiency virus, a patient group for which it is in general difficult to detect M. tuberculosis-specific antibodies.
检测结核分枝杆菌感染需要改进诊断试剂,而开发血清学诊断试验将补充现有的诊断方法。本研究的目的是鉴定用于未来结核病血清学诊断的新型血清学靶点。我们在大肠杆菌中克隆并表达了35种结核分枝杆菌蛋白作为重组蛋白,并分析了它们的血清学诊断潜力。通过两步筛选过程,鉴定出四种优质血清抗原,即TB9.7、TB15.3、TB16.3和TB51,之前均未被描述过。用来自结核病流行地区和非流行地区的涂片阳性和涂片阴性结核病患者的血清样本对这四种新型抗原进行检测,识别频率在31%至93%之间,特异性至少为97%。最有效的单一抗原是TB16.3,丹麦住院结核病患者样本的敏感性为48%至55%,非洲结核病患者样本的敏感性为88%至98%。重要的是,超过85%的人类免疫缺陷病毒合并感染结核病患者的样本识别出了TB16.3和TB9.7抗原,而这一患者群体通常很难检测到结核分枝杆菌特异性抗体。