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PCR 作为血液系统疾病患者侵袭性曲霉菌病的筛查试验:一项初步研究。

PCR as a screening test for invasive aspergillosis in haematological patients: a pilot study.

机构信息

Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, Brazil.

出版信息

Mycopathologia. 2014 Feb;177(1-2):111-4. doi: 10.1007/s11046-013-9718-0. Epub 2013 Dec 6.

DOI:10.1007/s11046-013-9718-0
PMID:24309908
Abstract

Invasive aspergillosis is a leading cause of morbidity and mortality in immunocompromised patients, particularly in individuals with haematological malignancy and in haematopoietic stem cell transplant recipients. Nowadays, the galactomannan (GM) assay has been widely used as an indication of invasive aspergillosis, even though the test is known to generate false-positive results. The aim of this study was to compare the performance of GM and real-time PCR (qPCR) to detected Aspergillus in blood samples obtained from high-risk haematological patients. Haematological patients were screened twice weekly with GM testing, which was performed by the Platelia ELISA kit. An additional sample of whole blood (4 ml) was obtained for the purpose of qPCR testing. Sixty-four samples from 12 patients with haematopoietic stem cell transplant or haematological malignancy were studied. The overall accordance between GM and qPCR tests was 96.9 % (62 samples). Only two samples showed contradictory results, with positive GM test and negative real-time PCR results. Based on the high concordance between GM and qPCR in terms of negative results, the main utility of qPCR could be in the confirmation of positive results seen with GM testing.

摘要

侵袭性曲霉病是免疫功能低下患者发病率和死亡率的主要原因,特别是在血液恶性肿瘤和造血干细胞移植受者中。如今,半乳甘露聚糖(GM)检测已广泛用于侵袭性曲霉病的诊断,尽管该检测已知会产生假阳性结果。本研究旨在比较 GM 和实时 PCR(qPCR)检测血液样本中曲霉的性能,这些血液样本来自高危血液系统疾病患者。通过 Platelia ELISA 试剂盒进行 GM 检测,每周对血液系统疾病患者进行两次筛查。为了进行 qPCR 检测,还采集了 4 毫升全血的额外样本。研究了 12 例造血干细胞移植或血液恶性肿瘤患者的 64 个样本。GM 和 qPCR 检测的总体符合率为 96.9%(62 个样本)。只有两个样本的结果存在差异,GM 检测呈阳性,而实时 PCR 结果为阴性。基于 GM 和 qPCR 在阴性结果方面的高度一致性,qPCR 的主要用途可能是确认 GM 检测呈阳性的结果。

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本文引用的文献

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Br J Haematol. 2013 May;161(4):517-24. doi: 10.1111/bjh.12285. Epub 2013 Mar 11.
2
Multicenter comparison of serum and whole-blood specimens for detection of Aspergillus DNA in high-risk hematological patients.多中心比较高危血液病患者血清和全血标本检测曲霉 DNA。
J Clin Microbiol. 2013 May;51(5):1445-50. doi: 10.1128/JCM.03322-12. Epub 2013 Feb 20.
3
A MIQE-compliant real-time PCR assay for Aspergillus detection.
符合 MIQE 指南的曲霉属实时 PCR 检测方法。
PLoS One. 2012;7(7):e40022. doi: 10.1371/journal.pone.0040022. Epub 2012 Jul 10.
4
Reshuffling of Aspergillus fumigatus cell wall components chitin and β-glucan under the influence of caspofungin or nikkomycin Z alone or in combination.在单独或联合使用卡泊芬净或尼克霉素 Z 的影响下,烟曲霉细胞壁成分几丁质和β-葡聚糖的重排。
Antimicrob Agents Chemother. 2012 Mar;56(3):1595-8. doi: 10.1128/AAC.05323-11. Epub 2011 Dec 27.
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Critical stages of extracting DNA from Aspergillus fumigatus in whole-blood specimens.从全血标本中提取烟曲霉 DNA 的关键阶段。
J Clin Microbiol. 2010 Oct;48(10):3753-5. doi: 10.1128/JCM.01466-10. Epub 2010 Aug 18.
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