Academic Unit of Clinical & Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.
Academic Unit of Cancer Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.
Thorax. 2017 Oct;72(10):946-949. doi: 10.1136/thoraxjnl-2016-209397. Epub 2017 Feb 3.
The impact of immunosuppression on interferon-γ release assays and novel cytokine biomarkers of TB infection, mycobacteria-specific IL-2, IP-10 and TNF-α responses was investigated in an ex vivo model. Cytokine responses in standard QuantiFERON-TB Gold in-Tube (QFT-GIT) assays were compared with duplicate assays containing dexamethasone or infliximab. Dexamethasone converted QFT-GIT results from positive to negative in 30% of participants. Antigen-stimulated interferon-γ, IL-2 and TNF-α responses were markedly reduced, but IP-10 responses were preserved. Infliximab caused QFT-GIT result conversion in up to 30% of participants and substantial reductions in all cytokine responses. Therefore, corticosteroids and anti-TNF-α agents significantly impair interferon-γ release assay performance. IP-10 may be a more robust TB biomarker than interferon-γ in patients receiving corticosteroids.
在体外模型中研究了免疫抑制对干扰素-γ释放试验(IGRA)和新型结核感染细胞因子生物标志物(如结核分枝杆菌特异性 IL-2、IP-10 和 TNF-α 反应)的影响。比较了标准的 QuantiFERON-TB Gold in-Tube(QFT-GIT)检测试剂盒中的细胞因子反应与含有地塞米松或英夫利昔单抗的重复检测试剂盒。地塞米松使 30%的参与者的 QFT-GIT 结果由阳性转为阴性。抗原刺激的干扰素-γ、IL-2 和 TNF-α 反应明显降低,但 IP-10 反应得到保留。英夫利昔单抗导致高达 30%的参与者的 QFT-GIT 结果发生转换,并使所有细胞因子反应显著降低。因此,皮质类固醇和抗 TNF-α 药物显著影响干扰素-γ释放试验的性能。在接受皮质类固醇治疗的患者中,IP-10 可能是比干扰素-γ更可靠的结核生物标志物。