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支气管肺泡灌洗酶联免疫斑点法诊断 HIV 感染患者中的菌阴肺结核。

Bronchoalveolar lavage enzyme-linked immunospot for diagnosis of smear-negative tuberculosis in HIV-infected patients.

机构信息

Division of Pulmonary and Critical Care Medicine, San Francisco General Hospital, University of California San Francisco, San Francisco, California, United States of America.

出版信息

PLoS One. 2012;7(6):e39838. doi: 10.1371/journal.pone.0039838. Epub 2012 Jun 26.

Abstract

BACKGROUND

Peripheral blood interferon-gamma release assays (IGRAs) have sub-optimal sensitivity and specificity for diagnosis of active pulmonary tuberculosis (TB). However, assessment of local immune responses has been reported to improve the accuracy of TB diagnosis.

METHODS

We enrolled HIV-infected adults with cough ≥2 weeks' duration admitted to Mulago Hospital in Kampala, Uganda and referred for bronchoscopy following two negative sputum acid-fast bacillus smears. We performed an ELISPOT-based IGRA (T-SPOT.TB®, Oxford Immunotec, Oxford, UK) using peripheral blood and bronchoalveolar lavage (BAL) fluid mononuclear cells, and determined the accuracy of IGRAs using mycobacterial culture results as a reference standard.

RESULTS

94 HIV-infected patients with paired peripheral blood and BAL IGRA results were included. The study population was young (median age 34 years [IQR 28-40 years]) and had advanced HIV/AIDS (median CD4+ T-lymphocyte count 60 cells/µl [IQR 22-200 cells/µl]). The proportion of indeterminate IGRA results was higher in BAL fluid than in peripheral blood specimens (34% vs. 14%, difference 20%, 95% CI 7-33%, p = 0.002). BAL IGRA had moderate sensitivity (73%, 95% CI 50-89%) but poor specificity (48%, 95% CI 32-64%) for TB diagnosis. Sensitivity was similar (75%, 95% CI 57-89%) and specificity was higher (78%, 95% CI 63-88%) when IGRA was performed on peripheral blood.

CONCLUSIONS

BAL IGRA performed poorly for the diagnosis of smear-negative TB in a high HIV/TB burden setting. Further studies are needed to examine reasons for the large proportion of indeterminate results and low specificity of BAL IGRA for active TB in high HIV/TB burden settings.

摘要

背景

外周血干扰素-γ释放检测(IGRAs)在诊断活动性肺结核(TB)方面的敏感性和特异性均不理想。然而,局部免疫反应的评估已被报道可提高 TB 诊断的准确性。

方法

我们招募了在乌干达坎帕拉的穆拉戈医院因咳嗽持续≥2 周且两次痰抗酸杆菌涂片阴性而接受支气管镜检查的 HIV 感染成人。我们使用外周血和支气管肺泡灌洗液(BAL)单核细胞进行基于 ELISPOT 的 IGRA(T-SPOT.TB ®,Oxford Immunotec,牛津,英国),并使用分枝杆菌培养结果作为参考标准确定 IGRAs 的准确性。

结果

纳入了 94 例 HIV 感染患者的外周血和 BAL IGRA 结果。研究人群年龄较轻(中位年龄 34 岁[IQR 28-40 岁]),且患有晚期 HIV/AIDS(中位 CD4+T 淋巴细胞计数 60 个/µl[IQR 22-200 个/µl])。BAL 液中不确定的 IGRA 结果比例高于外周血标本(34% vs. 14%,差异为 20%,95%CI 7-33%,p=0.002)。BAL IGRA 对 TB 诊断的敏感性(73%,95%CI 50-89%)中等,但特异性(48%,95%CI 32-64%)较差。当在外周血中进行 IGRA 时,敏感性相似(75%,95%CI 57-89%),特异性更高(78%,95%CI 63-88%)。

结论

在高 HIV/TB 负担环境中,BAL IGRA 对阴性涂片 TB 的诊断效果不佳。需要进一步研究以探讨在高 HIV/TB 负担环境中 BAL IGRA 对活动性 TB 出现大量不确定结果和低特异性的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05c9/3383728/a214cb8c0c40/pone.0039838.g001.jpg

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