Rousselot Julie, Millon Laurence, Scherer Emeline, Bourgeois Nathalie, Imbert Sebastien, Dupont Damien, Debourgogne Anne, Maubon Danièle, Bellanger Anne Pauline, Thornton Christopher R
Parasitology-Mycology Department, Besançon University Hospital, Besançon, France.
CNRS, Chrono-environnement (UMR 6249), Université Marie et Louis Pasteur, Besançon, France.
J Clin Microbiol. 2025 Jun 18:e0022625. doi: 10.1128/jcm.00226-25.
A murine IgG2b monoclonal antibody, named TG11, binding to an extracellular polysaccharide antigen secreted by all fungi has been recently developed and integrated into a lateral-flow device (TG11-LFD). The aim of this study was to establish the clinical performance of TG11-LFD on bronchoalveolar lavage (BAL) fluids for the diagnosis of mucormycosis. Thirteen BAL samples from 13 patients with mucormycosis, all of which tested positive for qPCR ( [ = 5], [ = 2], [ = 5], and [ = 1]), were used to assess the TG11-LFD. We also selected 49 BAL samples from 25 patients with other invasive fungal infections (IFI) (aspergillosis, infection, candidiasis, and possible IFI) and from 20 patients without IFI for use as negative controls. The intensities of the test and control lines were recorded using a Cube reader. The diagnostic performance was assessed by analyzing the receiver operating characteristics (ROC) curve with the Jamovi software package (version 2.6.13). The area under the curve of the ROC curve was 0.739. Using a threshold value positivity ≤531 artificial units, the TG11-LFD test has a sensitivity and specificity of 76.92% and 75.51%, respectively, a positive predictive value of 45.45%, and a negative predictive value of 92.5%. In this study, we evaluated the performance of TG11-LFD on clinical samples for the first time and demonstrated its significant potential for enhancing the rapid detection of mucormycosis. Combining antigen detection with qPCR, as successfully applied in the diagnosis of aspergillosis, is likely to yield the most reliable diagnostic approach.IMPORTANCEMucormycosis is a severe emerging, invasive fungal disease caused by fungi in the order . The mortality rate remains high at approximately 50%. Rapid diagnosis and prompt initiation of targeted treatment are associated with an improved prognosis. Gold standard diagnostic procedures have poor sensitivity and long turnaround times. polymerase chain reaction in blood and respiratory samples has improved diagnosis, but this technique is not widely available due to high costs and the need for specialist equipment. A prototype lateral-flow device (TG11-LFD) incorporating a mouse monoclonal antibody, which binds to an extracellular polysaccharide antigen specific to fungi, has been recently developed. In this study, we evaluated for the first time the performance of the TG11-LFD test on clinical bronchoalveolar lavage fluids for diagnosing mucormycosis. With 76.92% sensitivity and 75.51% specificity, this innovative, simple, and affordable approach shows great potential for improving the rapid diagnosis of mucormycosis.
一种名为TG11的鼠源IgG2b单克隆抗体,可与所有真菌分泌的细胞外多糖抗原结合,最近已被开发出来并集成到一种侧向流动装置(TG11-LFD)中。本研究的目的是确定TG11-LFD在支气管肺泡灌洗(BAL)液中用于诊断毛霉病的临床性能。来自13例毛霉病患者的13份BAL样本均经qPCR检测呈阳性([=5],[=2],[=5],[=1]),用于评估TG11-LFD。我们还从25例患有其他侵袭性真菌感染(IFI)(曲霉病、感染、念珠菌病和可能的IFI)的患者以及20例无IFI的患者中选取了49份BAL样本作为阴性对照。使用Cube读数仪记录检测线和对照线的强度。通过使用Jamovi软件包(版本2.6.13)分析受试者工作特征(ROC)曲线来评估诊断性能。ROC曲线下面积为0.739。使用阳性阈值≤531人工单位时,TG11-LFD检测的灵敏度和特异性分别为76.92%和75.51%,阳性预测值为45.45%,阴性预测值为92.5%。在本研究中,我们首次评估了TG11-LFD在临床样本上的性能,并证明了其在增强毛霉病快速检测方面的巨大潜力。将抗原检测与qPCR相结合,如同成功应用于曲霉病诊断一样,可能会产生最可靠的诊断方法。
重要性
毛霉病是一种由目真菌引起的严重新兴侵袭性真菌疾病。死亡率仍然很高,约为50%。快速诊断和及时开始靶向治疗与改善预后相关。金标准诊断程序灵敏度低且周转时间长。血液和呼吸道样本中的聚合酶链反应改善了诊断,但由于成本高和需要专业设备,该技术尚未广泛应用。最近开发了一种原型侧向流动装置(TG11-LFD),其包含一种小鼠单克隆抗体,可与毛霉目真菌特有的细胞外多糖抗原结合。在本研究中,我们首次评估了TG11-LFD检测在临床支气管肺泡灌洗液中诊断毛霉病的性能。这种创新、简单且经济实惠的方法灵敏度为76.92%,特异性为75.51%,在改善毛霉病快速诊断方面显示出巨大潜力。