Jiang Weimin, Shao Lingyun, Zhang Ying, Zhang Shu, Meng Chengyan, Xu Yunya, Huang Lingli, Wang Yun, Wang Ying, Weng Xinhua, Zhang Wenhong
Department of Infectious Diseases, Huashan Hospital, Fudan University, Shanghai 200040, PR China.
BMC Immunol. 2009 May 28;10:31. doi: 10.1186/1471-2172-10-31.
An accurate test for Mycobacterium tuberculosis infection is urgently needed in immunosuppressed populations. The aim of this study was to investigate the diagnostic power of enzyme-linked immunospot (ELISPOT)-based IFN-gamma release assay in detecting active and latent tuberculosis in HIV-infected population in bacillus Calmette-Guerin (BCG)-vaccinated area. A total of 100 HIV-infected individuals including 32 active tuberculosis patients were recruited. An ELISPOT-based IFN-gamma release assay, T-SPOT.TB, was used to evaluate the M. tuberculosis ESAT-6 and CFP-10 specific IFN-gamma response. Tuberculin skin test (TST) was performed for all recruited subjects.
The subjects were divided into group HIV+ATB (HIV-infected individuals with active tuberculosis, n = 32), group HIV+LTB (HIV-infected individuals with positive results of T-SPOT.TB assay, n = 46) and group HIV only (HIV-infected individuals with negative results of T-SPOT.TB assay and without evidence of tuberculosis infection, n = 22). In group HIV+ATB and HIV+LTB, T-SPOT.TB positive rate in subjects with TST <5 mm were 50% (16/32) and 41.3% (19/46), respectively. Individuals in group HIV+ATB and HIV+LTB with CD4+ T cells <500/microl, T-SPOT.TB showed a higher sensitivity than TST (64.5% vs. 22.6% and 62.2% vs. 29.7%, respectively, both P < 0.0001). In addition, the sensitivity of T-SPOT.TB assay in group HIV+ATB increased to >85% in patients with TB treatment for less than 1 month and CD4+ T cells > or = 200/microl, while for patients treated for more than 3 months and CD4+ T cells <200/microl, the sensitivity was decreased to only 33.3%. Furthermore, the results could be generated by T-SPOT.TB assay within 24 hours, which was more rapid than TST with 48-72 hours.
ELISPOT-based IFN-gamma release assay is more sensitive and rapid for the diagnosis of TB infection in Chinese HIV-infected individuals with history of BCG vaccination, and could be an effective tool for guiding preventive treatment with isoniazid in latently infected people and for TB control in China.
免疫抑制人群迫切需要一种准确检测结核分枝杆菌感染的方法。本研究旨在探讨基于酶联免疫斑点(ELISPOT)的γ-干扰素释放试验在卡介苗(BCG)接种地区检测HIV感染人群活动性和潜伏性结核的诊断效能。共招募了100名HIV感染者,其中包括32例活动性结核患者。采用基于ELISPOT的γ-干扰素释放试验(T-SPOT.TB)评估结核分枝杆菌早期分泌性抗原靶6(ESAT-6)和培养滤液蛋白10(CFP-10)特异性γ-干扰素反应。对所有招募的受试者进行结核菌素皮肤试验(TST)。
受试者分为HIV+ATB组(HIV感染的活动性结核患者,n = 32)、HIV+LTB组(T-SPOT.TB试验结果为阳性的HIV感染个体,n = 46)和单纯HIV组(T-SPOT.TB试验结果为阴性且无结核感染证据的HIV感染个体,n = 22)。在HIV+ATB组和HIV+LTB组中,TST<5 mm的受试者T-SPOT.TB阳性率分别为50%(16/32)和41.3%(19/46)。HIV+ATB组和HIV+LTB组中CD4+T细胞<500/μl的个体,T-SPOT.TB的敏感性高于TST(分别为64.5%对22.6%和62.2%对29.7%,P均<0.0001)。此外,HIV+ATB组中结核治疗时间少于1个月且CD4+T细胞≥200/μl的患者,T-SPOT.TB试验的敏感性增至>85%,而治疗时间超过3个月且CD4+T细胞<200/μl的患者,敏感性降至仅33.3%。此外,T-SPOT.TB试验可在24小时内得出结果,比48 - 72小时的TST更快。
基于ELISPOT的γ-干扰素释放试验对有卡介苗接种史的中国HIV感染个体的结核感染诊断更敏感、快速,可为潜伏感染人群的异烟肼预防性治疗及中国的结核病防控提供有效工具。