结核分枝杆菌特异性CD4 t细胞评分区分结核感染与疾病

Andrej Mantei, Tim Meyer, M. Schürmann, C. Beßler, H. Bias, D. Krieger, T. Bauer, P. Bacher, J. Helmuth, H. Volk, D. Schürmann, A. Scheffold, C. Meisel
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引用次数: 4

摘要

背景快速和可靠的结核病诊断检查仍然是一个主要的卫生保健目标。特别是,用现有的诊断工具区分结核感染和结核病是具有挑战性和耗时的。这项研究旨在建立一种标准化的血液检测方法,基于对结核病抗原反应性CD4+ t细胞作为结核病阶段特异性免疫状态传感器的多参数分析,快速可靠地区分结核病感染和结核病。方法在德国柏林当地三级医院招募157例疑似结核感染或结核病的hiv阴性受试者。检测外周血单核细胞CD4+ t细胞对结核分枝杆菌抗原纯化蛋白衍生物和早期分泌抗原靶蛋白6kda /培养滤液蛋白10的反应。通过CD154的表面表达鉴定TB抗原反应t细胞的活化状态,并根据增殖标志物Ki-67、活化标志物CD38和HLA-DR的表达谱评估其活化状态。使用来自81名临床确诊的结核病感染(n=34)或培养证实的肺部或肺外结核病(n=47)的受试者的数据,从表达谱中得出12个参数并将其整合到评分系统中。结果使用评分系统,我们的检测方法(TB- flow assay)能够可靠地区分肺部和肺外结核病感染,具有高灵敏度(90.9%)和特异性(93.3%),这一点得到了蒙特卡洛交叉验证的证实。结论该新型标准化TB- flow检测方法对肺部和肺外结核病的检测时间要求低,样品采集方便,灵敏度和特异性高,我们相信该方法将改善疑似结核病患者的检查,支持结核病的快速诊断和治疗决策。在一项前瞻性研究中,基于对结核病(TB)特异性CD4+ t细胞激活状态的分析,开发了一种评分系统,该系统能够以高灵敏度和特异性可靠地区分结核病感染和结核病https://bit.ly/3EFG4KX
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mycobacterium tuberculosis-specific CD4 T-cell scoring discriminates tuberculosis infection from disease
Background Rapid and reliable diagnostic work-up of tuberculosis (TB) remains a major healthcare goal. In particular, discrimination of TB infection from TB disease with currently available diagnostic tools is challenging and time consuming. This study aimed at establishing a standardised blood-based assay that rapidly and reliably discriminates TB infection from TB disease based on multiparameter analysis of TB antigen-reactive CD4+ T-cells acting as sensors for TB stage-specific immune status. Methods 157 HIV-negative subjects with suspected TB infection or TB disease were recruited from local tertiary care hospitals in Berlin (Germany). Peripheral blood mononuclear cells were analysed for CD4+ T-cells reactive to the Mycobacterium tuberculosis antigens purified protein derivative and early secretory antigenic target 6 kDa/culture filtrate protein 10. The activation state of TB antigen-reactive T-cells, identified by surface expression of CD154, was evaluated according to the expression profile of proliferation marker Ki-67 and activation markers CD38 and HLA-DR. Using data from 81 subjects with clinically confirmed TB infection (n=34) or culture-proven pulmonary or extrapulmonary TB disease (n=47), 12 parameters were derived from the expression profile and integrated into a scoring system. Results Using the scoring system, our assay (TB-Flow Assay) allowed reliable discrimination of TB infection from both pulmonary and extrapulmonary TB disease with high sensitivity (90.9%) and specificity (93.3%) as was confirmed by Monte-Carlo cross-validation. Conclusion With low time requirement, ease of sample collection, and high sensitivity and specificity both for pulmonary and extrapulmonary TB disease, we believe this novel standardised TB-Flow Assay will improve the work-up of patients with suspected TB disease, supporting rapid TB diagnosis and facilitating treatment decisions. In a prospective study, a scoring system based on analysis of the activation state of tuberculosis (TB)-specific CD4+ T-cells was developed that allows reliable discrimination of TB infection and TB disease with high sensitivity and specificity https://bit.ly/3EFG4KX
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