Ambasta Anshula, Carson Julie, Church Deirdre L
Medicine, University of Calgary, Calgary, Alta.
Division of Microbiology, University of Calgary, Calgary, Alta Calgary Laboratory Services, and the Departments of Pathology & Laboratory Medicine, University of Calgary, Calgary, Alta.
Med Mycol. 2015 Aug;53(6):531-57. doi: 10.1093/mmy/myv026. Epub 2015 May 30.
Invasive aspergillosis (IA) is an opportunistic infection that is often life threatening in the immunocompromised host. Early diagnosis is critical, especially given the efficacy and availability of several new anti-fungal therapies. Current (2008) diagnostic criteria have limited ability to detect early infection and are aimed at establishing disease. Although histopathology and culture techniques have traditionally been used to make a proven diagnosis of IA, their dependence on tissue samples and slow turnaround times hamper early confirmation of IA. Serologic detection of circulating galactomannan and 1,3-β-D-glucan fungal biomarkers show promise for improving the diagnosis of IA, and their use is included in the EORTC/MSG diagnostic criteria for IA. Numerous studies have evaluated the diagnostic performance of these two biomarkers and shown that they have suboptimal sensitivity when used alone for early diagnosis of proven IA. Currently available molecular assays also suffer from a lack of standardization. Evaluation of the use of different combinations of test methods to enhance diagnostic accuracy is also being done but prompt, accurate diagnosis of IA remains a clinical and diagnostic challenge. The clinical validity and limitations of biomarkers and current molecular methods for the early diagnosis of IA are summarized in this review with respect to the different patient populations at risk for this serious infection.
侵袭性曲霉病(IA)是一种机会性感染,在免疫功能低下的宿主中常常危及生命。早期诊断至关重要,特别是考虑到几种新型抗真菌疗法的疗效和可及性。当前(2008年)的诊断标准检测早期感染的能力有限,其目的是确诊疾病。尽管传统上一直使用组织病理学和培养技术来确诊IA,但它们对组织样本的依赖性以及周转时间长阻碍了IA的早期确诊。循环半乳甘露聚糖和1,3-β-D-葡聚糖真菌生物标志物的血清学检测有望改善IA的诊断,并且它们的应用已纳入IA的欧洲癌症研究与治疗组织/美国国立医学研究院(EORTC/MSG)诊断标准。大量研究评估了这两种生物标志物的诊断性能,结果表明,单独使用它们对确诊IA进行早期诊断时,敏感性欠佳。目前可用的分子检测方法也缺乏标准化。目前也在评估使用不同组合的检测方法以提高诊断准确性,但IA的快速、准确诊断仍然是一项临床和诊断挑战。本综述针对有这种严重感染风险的不同患者群体,总结了IA早期诊断中生物标志物和当前分子方法的临床有效性及局限性。