Use of real-time PCR on blood samples for diagnosis of invasive aspergillosis

被引:186
作者
Kami, M
Fukui, T
Ogawa, S
Kazuyama, Y
Machida, U
Tanaka, Y
Kanda, Y
Kashima, T
Yamazaki, Y
Hamaki, T
Mori, S
Akiyama, H
Mutou, Y
Sakamaki, H
Osumi, K
Kimura, S
Hirai, H
机构
[1] Toranomon Gen Hosp, Dept Hematol, Minato Ku, Tokyo 1058470, Japan
[2] Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Tokyo, Japan
[3] Univ Tokyo, Grad Sch Med, Dept Pathol, Tokyo, Japan
[4] Univ Tokyo, Grad Sch Med, Dept Infect Dis Control, Tokyo, Japan
[5] Tokyo Metropolitan Komagome Hosp, Dept Hematol, Tokyo, Japan
[6] Otsuka Pharmaceut Co Ltd, Otsuka Assay Labs, Tokushima 77101, Japan
关键词
D O I
10.1086/323337
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We developed a new quantitative system for diagnosis of invasive pulmonary aspergillosis (IPA) using realtime automated polymerase chain reaction (PCR). Intra-assay and interassay precision rates for in vitro examination were 2.53% and 2.20%, respectively, and the linearity of this assay was obtained when there were > 20 copies/well. We examined 323 samples taken from 122 patients with hematological malignancies, including 33 patients with IPA and 89 control patients. Blood samples were subjected to PCR antigen detection methods, using enzyme-linked immunosorbent assay (ELISA) and determination of plasma (1-->3)-beta -D-glucan (BDG) concentration. The sensitivities of PCR, ELISA, and BDG measurement for diagnosis of IPA were 79%, 58%, and 67%, respectively; the specificities were 92%, 97%, and 84%. Positive findings on PCR preceded those of computed tomography by days, those of BDG measurement by days, and those of ELISA -0.3 +/- 6.6 by 2.8 +/- 4.1 days. Real-time PCR was sensitive for IPA diagnosis, and quantitation was accurate.
引用
收藏
页码:1504 / 1512
页数:9
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