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

Citation
M. Kami et al., Use of real-time PCR on blood samples for diagnosis of invasive aspergillosis, CLIN INF D, 33(9), 2001, pp. 1504-1512
Citations number
25
Categorie Soggetti
Clinical Immunolgy & Infectious Disease",Immunology
Journal title
CLINICAL INFECTIOUS DISEASES
ISSN journal
10584838 → ACNP
Volume
33
Issue
9
Year of publication
2001
Pages
1504 - 1512
Database
ISI
SICI code
1058-4838(20011101)33:9<1504:UORPOB>2.0.ZU;2-S
Abstract
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 obtaine d when there were > 20 copies/well. We examined 323 samples taken from 122 patients with hematological malignancies, including 33 patients with IPA an d 89 control patients. Blood samples were subjected to PCR antigen detectio n methods, using enzyme-linked immunosorbent assay (ELISA) and determinatio n of plasma (1-->3)-beta -D-glucan (BDG) concentration. The sensitivities o f PCR, ELISA, and BDG measurement for diagnosis of IPA were 79%, 58%, and 6 7%, respectively; the specificities were 92%, 97%, and 84%. Positive findin gs on PCR preceded those of computed tomography by days, those of BDG measu rement by days, and those of ELISA -0.3 +/- 6.6 by 2.8 +/- 4.1 days. Real-t ime PCR was sensitive for IPA diagnosis, and quantitation was accurate.