DETECTION OF CYTOMEGALOVIRUS IN LIVER-TRANSPLANT BIOPSIES - A COMPARISON OF LIGHT-MICROSCOPY, IMMUNOHISTOCHEMISTRY, DUPLEX PCR, AND NESTED PCR

Citation
Ja. Brainard et al., DETECTION OF CYTOMEGALOVIRUS IN LIVER-TRANSPLANT BIOPSIES - A COMPARISON OF LIGHT-MICROSCOPY, IMMUNOHISTOCHEMISTRY, DUPLEX PCR, AND NESTED PCR, Transplantation, 57(12), 1994, pp. 1753-1757
Citations number
30
Categorie Soggetti
Immunology,Surgery
Journal title
ISSN journal
00411337
Volume
57
Issue
12
Year of publication
1994
Pages
1753 - 1757
Database
ISI
SICI code
0041-1337(1994)57:12<1753:DOCILB>2.0.ZU;2-J
Abstract
The polymerase chain reaction was used to detect cytomegalovirus (CMV) in 91 formalin fixed paraffin-embedded needle biopsies from 38 liver transplant patients with allograft dysfunction. Thirty donor liver bio psies served as negative controls. PCR results were compared with ligh t microscopy (LM), immunohistochemical staining (IH) for CMV early and late antigen, and clinical data. Primers to the major immediate early gene (MIE) and the viral DNA polymerase gene were duplex amplified. P CR product was reamplified with a nested primer set for the MIE and co nfirmed by electrophoretic mobilities and dot blotting. Primers for hu man beta-hemoglobin were used as internal controls. Seventeen of 38 pa tients had clinical evidence of cytomegalovirus disease, 12 of these w ere IH-positive, 14 were LM-positive, 15 were duplex PCR-positive and 17 were nested PCR-positive. In addition, duplex PCR was positive in o ne patient without other evidence of CMV disease, while nested PCR was positive in 12 such patients. The sensitivity and negative predictive value of nested PCR was 100%-however, the specificities and positive predictive values were only 42.9 and 58.6%, respectively. The control group was completely negative by LM, IH, and duplex PCR, however, 6 of 30 patients were nested PCR-positive. The number of nested positive, duplex-negative patients without CMV disease was significantly greater in the transplant group versus the control group (12/21 vs. 6/30, P<0 .009). The incidence of IgG seropositivity was also significantly grea ter in the transplant group versus the controls (29/32 vs. 15/24, P<0. 02). We conclude that nested PCR may be an overly sensitive technique for the detection of clinically relevant CMV disease. A negative neste d PCR assay for CMV may, however, help rule out symptomatic CMV infect ion in an individual case. Duplex PCR showed little advantage over LM, while M was confirmatory but did not add any new information in this study.