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Mycobacteria-specific cytokine responses detect tuberculosis infection and distinguish latent from active tuberculosis

机译:分枝杆菌特异性细胞因子反应检测结核感染并区分潜伏性和活动性结核病

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摘要

RATIONALE: Current immunodiagnostic tests for tuberculosis (TB), including the tuberculin skin test and IFN-? release assay (IGRA), have significant limitations, which include their inability to distinguish between latent TB infection (LTBI) and active TB, a distinction critical for clinical management.OBJECTIVES: To identify mycobacteria-specific cytokine biomarkers that characterize TB infection, determine their diagnostic performance characteristics, and establish whether these biomarkers can distinguish between LTBI and active TB.METHODS: A total of 149 children investigated for TB infection were recruited; all participants underwent a tuberculin skin test and QuantiFERON-TB Gold assay. In parallel, whole-blood assays using early secretory antigenic target-6, culture filtrate protein-10, and PPD as stimulatory antigens were undertaken, and cytokine responses were determined by xMAP multiplex assays.MEASUREMENTS AND MAIN RESULTS: IFN-?, interferon-inducible protein-10 (IP-10), tumor necrosis factor (TNF)-?, IL-1ra, IL-2, IL-13, and MIP-1? (macrophage inflammatory protein-1?) responses were significantly higher in LTBI and active TB cases than in TB-uninfected individuals, irrespective of the stimulant. Receiver operating characteristic analyses showed that IP-10, TNF-?, and IL-2 responses achieved high sensitivity and specificity for the distinction between TB-uninfected and TB-infected individuals. TNF-?, IL-1ra, and IL-10 responses had the greatest ability to distinguish between LTBI and active TB cases; the combinations of TNF-?/IL-1ra and TNF-?/IL-10 achieved correct classification of 95.5% and 100% of cases, respectively.CONCLUSIONS: We identified several mycobacteria-specific cytokine biomarkers with the potential to be exploited for immunodiagnosis. Incorporation of these biomarkers into future immunodiagnostic assays for TB could result in substantial gains in sensitivity and allow the distinction between LTBI and active TB based on a blood test alone.
机译:理由:当前针对结核病(TB)的免疫诊断测试,包括结核菌素皮肤测试和IFN-γ。释放试验(IGRA)有很大的局限性,包括无法区分潜伏性结核感染(LTBI)和活动性结核,这对临床管理至关重要。目标:要鉴定表征结核感染的分枝杆菌特异性细胞因子生物标志物,请确定诊断性能特征,并确定这些生物标记物是否能区分LTBI和活动性结核病。方法:总共招募了149名接受结核病感染调查的儿童。所有参与者均接受了结核菌素皮肤测试和QuantiFERON-TB Gold检测。平行进行了以早期分泌性抗原靶标6,培养物滤液蛋白10和PPD作为刺激性抗原的全血分析,并通过xMAP多重分析确定了细胞因子的反应。测量和主要结果:IFN-α,干扰素-诱导蛋白10(IP-10),肿瘤坏死因子(TNF)-α,IL-1ra,IL-2,IL-13和MIP-1α LTBI和活动性TB病例(巨噬细胞炎性蛋白1α)反应均显着高于未感染TB的个体,而与兴奋剂无关。接受者的工作特征分析表明,IP-10,TNF-α和IL-2应答对于区分未感染结核菌和未感染结核菌的个体具有很高的敏感性和特异性。 TNF-α,IL-1ra和IL-10反应对LTBI和活动性TB病例具有最大的区分能力。 TNF-α/ IL-1ra和TNF-α/ IL-10的组合分别正确分类为95.5%和100%的病例。结论:我们鉴定了几种分枝杆菌特异性细胞因子生物标志物,有可能被用于免疫诊断。 。将这些生物标记物纳入未来的结核病免疫诊断检测方法中,可大大提高敏感性,并仅根据血液检查即可区分LTBI和活动性TB。

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