暴露于结核病人群中结核分枝杆菌(Mtb)抗原触发免疫标记物的血液水平与结核感染状况和接受结核病预防治疗有关。

IF 2.8 3区 医学 Q3 IMMUNOLOGY Tuberculosis Pub Date : 2024-12-20 DOI:10.1016/j.tube.2024.102595
Petter Holmberg, Martina Janoušková, Tobias Schmidt, Ariane Neumann, Oskar Olsson, Per-Erik Isberg, Maja Reimann, Kristian Riesbeck, Sten Skogmar, Per Björkman
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Five persons without TBI were included as controls (IGRA-). Levels of 40 mediators related to TB immune control in blood incubated with Mtb antigens in the QuantiFERON-TB Plus® kit were assessed with electrochemiluminescence assay and compared between participant categories.</p><p><strong>Results: </strong>The concentration of 10 mediators (GM-CSF, interferon-γ, IL-2, I-TAC, IL-12, IP-10, I-309, MCP-2, MIG, and VEGF) significantly differed between IGRA + pre-treatment and IGRA-. A non-significant trend in levels of these markers was observed between IGRA + pre-treatment, IGRA + post-treatment and IGRA-. 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引用次数: 0

摘要

背景:用于结核感染(TBI)的干扰素γ释放试验(IGRAs)不能区分TBI谱的不同阶段(包括自发清除感染)。我们调查了结核预防治疗(TPT)期间有和没有TBI的人群中mtb特异性血液介质的模式。方法:纳入年龄在15-25岁、IGRA结果有效且排除结核病(TB)的近期可能暴露于Mtb的个体。TBI患者在TPT前(IGRA +预处理,n = 15)或TPT完成后(IGRA +后处理,n = 15)进行抽样。5例无TBI患者作为对照(IGRA-)。使用QuantiFERON-TB Plus®试剂盒检测与结核分枝杆菌抗原孵育的血液中与结核免疫控制相关的40种介质的水平,并用电化学发光法进行评估,并在参与者类别之间进行比较。结果:IGRA +预处理与IGRA-预处理间10种介质(GM-CSF、干扰素-γ、IL-2、I-TAC、IL-12、IP-10、I-309、MCP-2、MIG、VEGF)浓度有显著差异。这些标记物的水平在IGRA +处理前、IGRA +处理后和IGRA-之间没有显著的变化趋势。基于这些介质,我们确定了两个群体:A (n = 16),包括5个IGRA-, 4个IGRA +预处理,7个IGRA +处理后;B (n = 19),包括11个IGRA +预处理和8个IGRA +处理后。结论:在最近接触结核病的人群中,几种mtb触发介质的血浆水平与TBI状态有关,这表明有可能使用其他标志物来评估TBI状态。在TPT期间对这些介质进行纵向分析是有必要的,以探索这些标记物是否可用于评估mtb暴露个体中活杆菌持续存在的可能性。临床试验:govID: NCT05621343。
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Blood levels of Mycobacterium tuberculosis (Mtb)antigen-triggered immune markers in people exposed to tuberculosis with regard to Mtb infection status and receipt of tuberculosis preventive therapy.

Background: Interferon-γ release assays (IGRAs) for tuberculosis infection (TBI) cannot distinguish different stages of the TBI spectrum (including spontaneously cleared infection). We investigated patterns of Mtb-specific blood mediators in people with and without TBI during tuberculosis preventive therapy (TPT).

Methods: Individuals with likelihood of recent Mtb exposure, aged 15-25 years, with valid IGRA results, in whom tuberculosis (TB) had been excluded, were included. Persons with TBI were sampled prior to TPT (IGRA + pre-treatment, n = 15) or after completion of TPT (IGRA + post-treatment, n = 15). Five persons without TBI were included as controls (IGRA-). Levels of 40 mediators related to TB immune control in blood incubated with Mtb antigens in the QuantiFERON-TB Plus® kit were assessed with electrochemiluminescence assay and compared between participant categories.

Results: The concentration of 10 mediators (GM-CSF, interferon-γ, IL-2, I-TAC, IL-12, IP-10, I-309, MCP-2, MIG, and VEGF) significantly differed between IGRA + pre-treatment and IGRA-. A non-significant trend in levels of these markers was observed between IGRA + pre-treatment, IGRA + post-treatment and IGRA-. Based on these mediators two clusters were identified: A (n = 16), including 5 IGRA-, 4 IGRA + pre-treatment, 7 IGRA + post-treatment and B (n = 19), including 11 IGRA + pre-treatment and 8 IGRA + post-treatment.

Conclusion: Plasma levels of several Mtb-triggered mediators differed with regard to TBI status among persons recently exposed to TB, suggesting the potential for alternative markers to assess TBI status. Longitudinal analysis of these mediators during TPT is warranted to explore whether these markers can be used to assess likelihood of persistence of viable bacilli in Mtb-exposed individuals.

Clinicaltrials: govID:NCT05621343.

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来源期刊
Tuberculosis
Tuberculosis 医学-呼吸系统
CiteScore
4.60
自引率
3.10%
发文量
87
审稿时长
49 days
期刊介绍: Tuberculosis is a speciality journal focusing on basic experimental research on tuberculosis, notably on bacteriological, immunological and pathogenesis aspects of the disease. The journal publishes original research and reviews on the host response and immunology of tuberculosis and the molecular biology, genetics and physiology of the organism, however discourages submissions with a meta-analytical focus (for example, articles based on searches of published articles in public electronic databases, especially where there is lack of evidence of the personal involvement of authors in the generation of such material). We do not publish Clinical Case-Studies. Areas on which submissions are welcomed include: -Clinical TrialsDiagnostics- Antimicrobial resistance- Immunology- Leprosy- Microbiology, including microbial physiology- Molecular epidemiology- Non-tuberculous Mycobacteria- Pathogenesis- Pathology- Vaccine development. This Journal does not accept case-reports. The resurgence of interest in tuberculosis has accelerated the pace of relevant research and Tuberculosis has grown with it, as the only journal dedicated to experimental biomedical research in tuberculosis.
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