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基于质谱法检测泛真菌血清二糖对侵袭性真菌感染的诊断评估:涉及六个欧洲临床中心的合作研究结果。

Evaluation of Mass Spectrometry-Based Detection of Panfungal Serum Disaccharide for Diagnosis of Invasive Fungal Infections: Results from a Collaborative Study Involving Six European Clinical Centers.

机构信息

Laboratoire de Parasitologie Mycologie, CHU Lille, Université Lille, INSERM U995-LIRIC (Lille Inflammation Research International Centre), Lille, France.

Laboratoire de Parasitologie Mycologie, CHU Lille, Université Lille, INSERM U995-LIRIC (Lille Inflammation Research International Centre), Lille, France

出版信息

J Clin Microbiol. 2019 Apr 26;57(5). doi: 10.1128/JCM.01867-18. Print 2019 May.

DOI:10.1128/JCM.01867-18
PMID:30787140
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6498025/
Abstract

A mass spectrometry (MS) method that detects a serum disaccharide (DS) (MS-DS) was recently described for the diagnosis of invasive fungal infections (IFI). We carried out a European collaborative study to evaluate this assay. Patients with the following IFI were selected according to the availability of sera obtained at about the time that IFI was documented: invasive candidiasis (IC;  = 26 patients), invasive aspergillosis (IA;  = 19), and mucormycosis (MM;  = 23). Control sera originated from 20 neutropenic patients and 20 patients with bacteremia. MS-DS was carried out in blind manner for the diagnosis of IFI. A diagnosis of IC or IA was confirmed by detection of mannan (Man) or galactomannan (GM), respectively, associated with detection of (1,3)-β-d-glucan (BDG) in both infections. MM was detected by quantitative real-time PCR (qPCR). All tests discriminated sera from patients with IC from sera from control subjects with bacteremia ( ≤ 0.0009). For IC, the MS-DS sensitivity and specificity were 51% and 87%, respectively. MS-DS complemented the high specificity of Man monitoring. All tests discriminated sera from IA patients from sera from neutropenic controls ( ≤ 0.0009). For IA, MS-DS sensitivity and specificity were 64% and 95%, respectively. Only 13/36 serum samples from patients with MM were concordant by MS-DS and qPCR (6 were positive, and 7 were negative); 14 were positive by MS-DS alone. qPCR and MS-DS made a similar contribution to the diagnosis of MM. In patients undergoing long-term monitoring, the persistent circulation of serum disaccharide was observed, whereas DNA was detected only for a short period after initiation of treatment. MS-DS has an important role to play in the early diagnosis of IFI. Its panfungal nature and complementarity with other tests may justify its use in the management of IFI.

摘要

一种用于检测血清二糖(MS-DS)的质谱(MS)方法最近被描述用于侵袭性真菌感染(IFI)的诊断。我们进行了一项欧洲合作研究来评估该检测方法。根据获得疑似 IFI 时的血清样本,选择了以下 IFI 患者:侵袭性念珠菌病(IC;=26 例)、侵袭性曲霉病(IA;=19 例)和毛霉病(MM;=23 例)。对照血清来自 20 例中性粒细胞减少症患者和 20 例菌血症患者。MS-DS 以盲法进行,用于 IFI 的诊断。IC 或 IA 的诊断通过分别检测甘露聚糖(Man)或半乳甘露聚糖(GM),以及在两种感染中检测(1,3)-β-D-葡聚糖(BDG)来确认。MM 通过定量实时 PCR(qPCR)检测。所有检测方法均能区分 IC 患者血清与菌血症对照血清(≤0.0009)。对于 IC,MS-DS 的灵敏度和特异性分别为 51%和 87%。MS-DS 补充了 Man 监测的高特异性。所有检测方法均能区分 IA 患者血清与中性粒细胞减少症对照血清(≤0.0009)。对于 IA,MS-DS 的灵敏度和特异性分别为 64%和 95%。仅 36 例 MM 患者的血清样本中有 13 例通过 MS-DS 和 qPCR 检测结果一致(6 例阳性,7 例阴性);14 例仅通过 MS-DS 检测阳性。qPCR 和 MS-DS 对 MM 的诊断均有重要作用。在接受长期监测的患者中,观察到血清二糖的持续循环,而在开始治疗后仅短时间内检测到 DNA。MS-DS 在 IFI 的早期诊断中具有重要作用。其泛真菌特性和与其他检测方法的互补性可能使其在 IFI 的管理中具有应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/856a/6498025/f74b57a5b467/JCM.01867-18-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/856a/6498025/a10a51bbc736/JCM.01867-18-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/856a/6498025/5424bac02b85/JCM.01867-18-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/856a/6498025/901b5943075d/JCM.01867-18-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/856a/6498025/c66a04c7d001/JCM.01867-18-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/856a/6498025/648db9d5b8b9/JCM.01867-18-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/856a/6498025/f74b57a5b467/JCM.01867-18-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/856a/6498025/a10a51bbc736/JCM.01867-18-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/856a/6498025/5424bac02b85/JCM.01867-18-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/856a/6498025/901b5943075d/JCM.01867-18-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/856a/6498025/c66a04c7d001/JCM.01867-18-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/856a/6498025/648db9d5b8b9/JCM.01867-18-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/856a/6498025/f74b57a5b467/JCM.01867-18-f0006.jpg

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