Division of Pulmonary and Critical Care Medicine, University of California, San Francisco, San Francisco, USA.
BMC Infect Dis. 2010 Mar 20;10:75. doi: 10.1186/1471-2334-10-75.
T-cell interferon-gamma release assays (IGRAs) may have a role in the diagnosis of active tuberculosis when evaluating patients for whom standard microbiology has limited sensitivity. Our objective was to examine the accuracy of a commercial IGRA for diagnosis of active tuberculosis in HIV-infected persons.
We enrolled HIV-infected patients admitted to Mulago Hospital in Kampala, Uganda with cough > or = 2 weeks. All patients underwent standard medical evaluation. We collected peripheral blood specimens at enrollment and performed a commercial, ELISPOT-based IGRA according to the manufacturer's recommendations. IGRA sensitivity and specificity were determined using mycobacterial culture results as the reference standard.
Overall, 236 patients were enrolled. The median CD4+ T-lymphocyte count was 49 cells/microl and 126 (53%) patients were diagnosed with active pulmonary tuberculosis. IGRAs were not performed in 24 (10%) patients due to insufficient mononuclear cell counts. In the remaining 212 patients, results were indeterminate in 54 (25%). IGRAs were positive in 95 of 158 (60%) patients with interpretable results. The proportion of positive test results was similar across CD4+ count strata. IGRA sensitivity was 73% and specificity 54%. IGRA results did not meaningfully alter the probability of active tuberculosis in patients with negative sputum smears.
An ELISPOT-based IGRA detected a high prevalence of latent tuberculosis infection in a hospitalized population of tuberculosis suspects with advanced HIV/AIDS but had limited utility for diagnosis of active tuberculosis in a high prevalence setting. Further research is needed to identify stronger and more specific immune responses in patients with active tuberculosis.
T 细胞干扰素-γ释放检测(IGRAs)在评估标准微生物学检测敏感性有限的疑似结核病患者时,可能对诊断活动性结核病有一定作用。我们的目的是检验一种商业 IGRA 用于诊断 HIV 感染者活动性结核病的准确性。
我们招募了乌干达坎帕拉市穆拉戈医院因咳嗽 > 或 = 2 周而住院的 HIV 感染者。所有患者都接受了标准的医学评估。我们在入组时采集外周血标本,并按照制造商的建议进行商业的、基于酶联免疫斑点的 IGRA。以分枝杆菌培养结果为参考标准,确定 IGRA 的敏感性和特异性。
共纳入 236 例患者。CD4+T 淋巴细胞计数中位数为 49 个/微升,126 例(53%)患者诊断为活动性肺结核。由于单核细胞计数不足,有 24 例(10%)患者未进行 IGRAs。在其余 212 例患者中,有 54 例(25%)结果为不确定。可解释结果的 158 例患者中,95 例(60%)IGRAs 阳性。阳性检测结果的比例在不同 CD4+计数层中相似。IGRA 的敏感性为 73%,特异性为 54%。IGRA 结果并不能显著改变涂片阴性的疑似结核病患者中结核病活动的概率。
在患有晚期 HIV/AIDS 的结核病疑似住院患者人群中,基于酶联免疫斑点的 IGRA 检测到潜伏性结核感染的高患病率,但在高患病率环境下对诊断活动性结核病的应用价值有限。需要进一步研究以确定活动性结核病患者更强和更特异的免疫应答。