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结核分枝杆菌抗原特异性γ-干扰素释放试验(T-SPOT.TB)的解读及可能调节检测结果的因素。

Interpretation of Mycobacterium tuberculosis antigen-specific IFN-gamma release assays (T-SPOT.TB) and factors that may modulate test results.

作者信息

Dheda K, Pooran A, Pai M, Miller R F, Lesley K, Booth H L, Scott G M, Akbar A N, Zumla A, Rook G A

机构信息

Division of Pulmonology, Department of Medicine, University of Cape Town, South Africa.

出版信息

J Infect. 2007 Aug;55(2):169-73. doi: 10.1016/j.jinf.2007.02.005. Epub 2007 Apr 19.

Abstract

BACKGROUND

Data about T cell antigen-specific (ESAT-6 and CFP-10) IFN-gamma release assays (IGRAs) during and after completion of anti-tuberculous (TB) treatment are limited and highly discordant. Thus, the utility of IGRAs as a surrogate marker of mycobacterial burden remain unclear.

METHODS

To investigate factors that modulate IGRA responses during anti-TB treatment we used a standardised assay (T-SPOT.TB) in 33 patients with culture positive tuberculosis.

RESULTS

Significantly more patients in the early (< or = 4 months of anti-TB treatment) rather than the late phase (> 4 months or completed anti-TB treatment) had positive IGRA responses [10/12 (83%) vs 4/21 (19%); p < or = 0.01]. Thus, 17/21 (81%) in the late phase or who had completed treatment (mean duration of treatment = 8.7 months) were IGRA negative, despite having robust antigen-specific recall proliferative responses. In these 17 patients prolonged incubation (5 days vs overnight), use of different antigen preparations (protein vs peptide) and addition of endotoxin, failed to elicit positive responses.

CONCLUSIONS

In treated TB patients the discordant IGRA data remain unexplained by variation in laboratory protocols and are more likely due to host or environmental factors. In a low burden setting IGRAs may be a promising surrogate marker of mycobacterial disease burden.

摘要

背景

关于抗结核治疗期间及治疗结束后T细胞抗原特异性(早期分泌性抗原靶6和培养滤液蛋白10)γ-干扰素释放试验(IGRAs)的数据有限且高度不一致。因此,IGRAs作为分枝杆菌负荷替代标志物的效用仍不明确。

方法

为了研究抗结核治疗期间调节IGRA反应的因素,我们对33例培养阳性肺结核患者使用了标准化检测方法(T-SPOT.TB)。

结果

抗结核治疗早期(≤4个月)而非晚期(>4个月或完成抗结核治疗)的患者中,IGRA反应呈阳性的显著更多[10/12(83%)对4/21(19%);p≤0.01]。因此,17/21(81%)处于晚期或已完成治疗(平均治疗持续时间=8.7个月)的患者IGRA呈阴性,尽管他们有强烈的抗原特异性回忆增殖反应。在这17例患者中,延长孵育时间(5天对过夜)、使用不同的抗原制剂(蛋白质对肽)以及添加内毒素,均未能引发阳性反应。

结论

在接受治疗的结核病患者中,不一致的IGRA数据无法用实验室方案的差异来解释,更可能是由于宿主或环境因素。在低负担情况下,IGRAs可能是分枝杆菌疾病负担的一个有前景的替代标志物。

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