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用于检测隐球菌抗原的商业试剂盒比较

Comparison of commercial kits for detection of cryptococcal antigen.

作者信息

Tanner D C, Weinstein M P, Fedorciw B, Joho K L, Thorpe J J, Reller L

机构信息

Clinical Microbiology Laboratory, Duke University Medical Center, Durham, North Carolina 27710.

出版信息

J Clin Microbiol. 1994 Jul;32(7):1680-4. doi: 10.1128/jcm.32.7.1680-1684.1994.

Abstract

Although kits to detect cryptococcal antigen are used widely to diagnose cryptococcal infection, the comparative performance of commercially available assays has not been evaluated in the past decade. Therefore, we compared the sensitives and specificities of five commercially available kits for detecting cryptococcal antigen (four latex agglutination test kits--Calas [Meridian Diagnostics])--Crypto-LA [International Biological Labs], Myco-Immune [MicroScan], and Immy [Immunomycologics]--and an enzyme immunoassay kit, Premier [Meridian Diagnostics]) with culture for the diagnosis of cryptococcal meningitis and fungemia. Of 182 cerebrospinal fluid (CSF) and 90 serum samples submitted for cryptococcal antigen and fungal culture, 49 (19 and 30 samples, respectively) from 20 patients had a culture positive for Cryptococcus neoformans. For CSF specimens, the sensitivities and specificities of all kits were comparable (sensitivity, 93 to 100%; specificity, 93 to 98%). There was a significant difference in sensitivities of the kits when serum samples were tested with the International Biological Labs and MicroScan kits, which do not pretreat serum with pronase. These kits were less sensitive (sensitivity, 83%) than the Immy and Meridian latex kits (sensitivity, 97%), which do pretreat with pronase. The sensitivity of the Meridian enzyme immunoassay kit was comparable to that of the pronase-containing latex kits. These kits were of equivalent specificities (93 to 100%) when testing serum. Some of the currently available kits have limitations that need to be recognized for proper interpretation of results. Specifically, the use of pronase on serum samples reduces the number of false-positive results, and a titer of < or = 1:4 can be a false-positive result when CSF samples are being tested.

摘要

尽管检测隐球菌抗原的试剂盒被广泛用于诊断隐球菌感染,但过去十年中尚未对市售检测方法的比较性能进行评估。因此,我们比较了五种市售检测隐球菌抗原试剂盒(四种乳胶凝集试验试剂盒——Calas [Meridian Diagnostics公司]、Crypto-LA [International Biological Labs公司]、Myco-Immune [MicroScan公司]和Immy [Immunomycologics公司]——以及一种酶免疫分析试剂盒,Premier [Meridian Diagnostics公司])与培养法在诊断隐球菌性脑膜炎和真菌血症方面的敏感性和特异性。在提交进行隐球菌抗原和真菌培养的182份脑脊液(CSF)和90份血清样本中,来自20名患者的49份样本(分别为19份和30份)培养出新型隐球菌阳性。对于脑脊液标本,所有试剂盒的敏感性和特异性相当(敏感性为93%至100%;特异性为93%至98%)。当用International Biological Labs公司和MicroScan公司的试剂盒检测血清样本时,试剂盒的敏感性存在显著差异,这两种试剂盒不使用链霉蛋白酶预处理血清。这些试剂盒的敏感性(83%)低于使用链霉蛋白酶预处理的Immy和Meridian乳胶试剂盒(敏感性为97%)。Meridian酶免疫分析试剂盒的敏感性与含链霉蛋白酶的乳胶试剂盒相当。检测血清时,这些试剂盒的特异性相当(93%至100%)。目前一些可用的试剂盒存在局限性,在正确解读结果时需要予以认识。具体而言,对血清样本使用链霉蛋白酶可减少假阳性结果的数量,并且检测脑脊液样本时滴度≤1:4可能为假阳性结果。

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