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
相关论文
共 28 条
[1]   Quantitative galactomannan detection is superior to PCR in diagnosing and monitoring invasive pulmonary aspergillosis in an experimental rat model [J].
Becker, MJ ;
de Marie, S ;
Willemse, D ;
Verbrugh, HA ;
Bakker-Woudenberg, IAJM .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (04) :1434-1438
[2]   Improved management of invasive pulmonary aspergillosis in neutropenic patients using early thoracic computed tomographic scan and surgery [J].
Caillot, D ;
Casasnovas, O ;
Bernard, A ;
Couaillier, JF ;
Durand, C ;
Cuisenier, B ;
Solary, E ;
Piard, F ;
Petrella, T ;
Bonnin, A ;
Couillault, G ;
Dumas, M ;
Guy, H .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (01) :139-147
[3]   ASPERGILLUS-FUNGEMIA - REPORT OF 2 CASES AND REVIEW [J].
DUTHIE, R ;
DENNING, DW .
CLINICAL INFECTIOUS DISEASES, 1995, 20 (03) :598-605
[4]   Detection and identification of fungal pathogens in blood by using molecular probes [J].
Einsele, H ;
Hebart, H ;
Roller, G ;
Loffler, J ;
Rothenhofer, I ;
Muller, CA ;
Bowden, RA ;
vanBurik, JA ;
Engelhard, D ;
Kanz, L ;
Schumacher, U .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (06) :1353-1360
[5]   Detection of Cryptosporidium parvum DNA in formed human feces by a sensitive PCR-based assay including uracil-N-glycosylase inactivation [J].
Gobet, P ;
Buisson, JC ;
Vagner, O ;
Naciri, M ;
Grappin, M ;
Comparot, S ;
Harly, G ;
Aubert, D ;
Varga, I ;
Camerlynck, P ;
Bonnin, A .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (01) :254-256
[6]   Real time quantitative PCR [J].
Heid, CA ;
Stevens, J ;
Livak, KJ ;
Williams, PM .
GENOME RESEARCH, 1996, 6 (10) :986-994
[7]   USE OF THE PASTOREX ASPERGILLUS ANTIGEN LATEX AGGLUTINATION-TEST FOR THE DIAGNOSIS OF INVASIVE ASPERGILLOSIS [J].
HOPWOOD, V ;
JOHNSON, EM ;
CORNISH, JM ;
FOOT, ABM ;
EVANS, EGV ;
WARNOCK, DW .
JOURNAL OF CLINICAL PATHOLOGY, 1995, 48 (03) :210-213
[8]   The limitation of circulating Aspergillus antigen detection methods for BMT recipients [J].
Kami, M ;
Tanaka, Y ;
Ogawa, S ;
Kanda, Y ;
Honda, H ;
Chiba, S ;
Mitani, K ;
Yazaki, Y ;
Hirai, H .
BONE MARROW TRANSPLANTATION, 1998, 22 (08) :832-833
[9]  
Kami M, 2000, HAEMATOLOGICA, V85, P745
[10]  
Kami M, 1999, CANCER, V86, P274, DOI 10.1002/(SICI)1097-0142(19990715)86:2&lt