Sester Martina, Altet-Gomez Neus, Andersen Åse Bengaard, Arias-Guillén Miguel, Avsar Korkut, Bakken Kran Anne-Marte, Bothamley Graham, Nordholm Breschel Anne Christine, Brown James, Chesov Dumitru, Ciobanu Nelly, Cirillo Daniela Maria, Crudu Valeriu, de Souza Galvao Malu, Dilektasli Asli Görek, Dominguez José, Duarte Raquel, Dyrhol-Riise Anne Ma, Goletti Delia, Hoffmann Harald, Ibraim Elmira, Kalsdorf Barbara, Krawczyk Marcin, Kunst Heinke, Lange Berit, Lipman Marc, Matteelli Alberto, Milkiewicz Piotr, Neyer David, Nitschke Martin, Oral Haluk Barbaros, Palacios-Gutiérrez Juan José, Petruccioli Elisa, Raszeja-Wyszomirska Joanna, Ravn Pernille, Rupp Jan, Spohn Hanna-Elisa, Toader Corina, Villar-Hernandez Raquel, Wagner Dirk, van Leth Frank, Martinez Leonardo, Pedersen Ole Skouvig, Lange Christoph
Department of Transplant and Infection Immunology, Saarland University, Homburg, Germany.
Center for Gender-specific Biology and Medicine (CGBM), Saarland University, Homburg, Germany.
Lancet Reg Health Eur. 2025 Aug 6;57:101416. doi: 10.1016/j.lanepe.2025.101416. eCollection 2025 Oct.
In low tuberculosis (TB)-endemic countries, tuberculosis preventive therapy (TPT) is recommended for immunocompromised individuals with a positive immunodiagnostic test. This study aimed to assess the performance of the QuantiFERON-TB Gold Plus (QFT+) assay and predictive power for future tuberculosis in immunocompromised individuals.
In this prospective observational study, immunocompromised adults ≥18 years of age including people living with HIV (PLHIV), chronic renal failure, rheumatoid arthritis, solid-organ transplantation or stem-cell transplantation, and immunocompetent adults with and without TB-disease were recruited at 21 sites in 11 European countries and tested with the QFT+ assay. Individuals without TB-disease were followed up for the development of tuberculosis. TB incidence rates (IR) were calculated, stratified by QFT+ results and acceptance of TPT. This study is registered with Clinicaltrials.gov, NCT02639936.
A total of 2663 individuals (1115 female, 1548 male) were enrolled from 03/11/2015 to 29/03/2019. Persons without tuberculosis were followed up for at least two years. Among 1758 immunocompromised individuals without active tuberculosis, 13.6% had positive QFT+ results. Sensitivity and specificity for TB-disease were 70.0% (52.1-83.3%) and 91.4% (89.6-92.9%), respectively, in immunocompromised, and 81.4% (76.6-85.3%) and 96.0% (92.5-97.9%), respectively, in immunocompetent individuals. During 2457 cumulative years of follow-up among 932 individuals with chronic renal failure, rheumatoid arthritis, solid-organ transplantation or stem-cell transplantation, including 83 persons with a positive QFT+ test without TPT, no-one developed active tuberculosis. In contrast, among 642 PLHIV without TPT, one with an indeterminate QFT+ and 3/30 individuals with a positive QFT+ developed active tuberculosis; all had detectable HIV-replication and low CD4 T-cell counts (incidence 4.1 (95% CI (1.3-12.4) per 100 person-years). No individuals receiving TPT developed active tuberculosis during 269 years of follow-up.
In immunocompromised individuals in low TB-endemic countries, the 2-year-risk for active tuberculosis was highest among PLHIV with detectable HIV-replication and low CD4-counts. In this study, the QFT+ assay did not strongly predict progression to active tuberculosis, which emphasises the need to incorporate additional risk factors.
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在结核病低流行国家,对于免疫诊断检测呈阳性的免疫功能低下个体,建议进行结核病预防性治疗(TPT)。本研究旨在评估全血γ干扰素释放试验增强版(QFT+)检测在免疫功能低下个体中的性能以及对未来结核病的预测能力。
在这项前瞻性观察性研究中,在11个欧洲国家的21个地点招募了年龄≥18岁的免疫功能低下成年人,包括艾滋病毒感染者(PLHIV)、慢性肾衰竭患者、类风湿关节炎患者、实体器官移植或干细胞移植患者,以及有或无结核病的免疫功能正常成年人,并采用QFT+检测进行检测。对无结核病的个体进行随访以观察结核病的发生情况。计算结核病发病率(IR),并按QFT+结果和TPT的接受情况进行分层。本研究已在Clinicaltrials.gov注册,注册号为NCT02639936。
从2015年11月3日至2019年3月29日,共招募了2663名个体(1115名女性,1548名男性)。对无结核病的个体进行了至少两年的随访。在1758名无活动性结核病的免疫功能低下个体中,13.6%的个体QFT+结果呈阳性。在免疫功能低下个体中,结核病的敏感性和特异性分别为70.0%(52.1 - 83.3%)和91.4%(89.6 - 92.9%),在免疫功能正常个体中分别为81.4%(76.6 - 85.3%)和96.0%(92.5 - 97.9%)。在932名患有慢性肾衰竭、类风湿关节炎、实体器官移植或干细胞移植的个体中,包括83名QFT+检测呈阳性但未接受TPT的个体,在2457人年的累计随访期间,无人发生活动性结核病。相比之下,在642名未接受TPT的PLHIV中,1名QFT+结果不确定的个体和3/30名QFT+检测呈阳性的个体发生了活动性结核病;所有这些个体均有可检测到的HIV复制且CD4 T细胞计数较低(发病率为每100人年4.1(95%CI(1.3 - 12.4))。在269人年的随访期间,接受TPT的个体均未发生活动性结核病。
在结核病低流行国家的免疫功能低下个体中,HIV复制可检测且CD4计数低的PLHIV发生活动性结核病的2年风险最高。在本研究中,QFT+检测并不能有力地预测进展为活动性结核病,这强调了纳入其他风险因素的必要性。
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