HCMV DNA detection and quantitation in the plasma and PBL of lung transplant recipients: COBAS Amplicor HCMV monitor test versus in-house quantitative HCMV PCR

被引:6
作者
Michaelides, A
Facey, D
Spelman, D
Wesselingh, S
Kotsimbos, T
机构
[1] Alfred Hosp, Dept Resp Med, Prahran, Vic 3181, Australia
[2] Alfred Hosp, Dept Microbiol, Prahran, Vic 3181, Australia
[3] Alfred Hosp, Infect Dis Unit, Prahran, Vic 3181, Australia
[4] Alfred Hosp, Dept Med, Prahran, Vic 3181, Australia
[5] Alfred Hosp, Heart Lung Transplant Serv, Prahran, Vic 3181, Australia
[6] Roche Diagnost Australia, Castle Hill, NSW 2154, Australia
关键词
COBAS Amplicor; human cytomegalovirus; lung transplant recipients; PCR; quantitation;
D O I
10.1016/S1386-6532(02)00272-X
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Human cytomegalovirus (HCMV) reactivation may cause severe disease in immunosuppressed patients. Quantitation of HCMV viral load in the blood has been shown to be important in predicting for HCMV disease, however the particular blood compartment that should be tested, plasma versus peripheral blood leukocytes (PBL), has been subject to debate. Objectives: To simultaneously compare HCMV viral loads in the PBL using an in-house quantitative HCMV polymerase chain reaction (PCR) assay and in the plasma using the commercially available COBAS Amplicor HCMV monitor test, in a cohort of lung transplant recipients (LTR). Study design: Sequential paired plasma and PBL samples were collected (n = 98) from a total of 21 LTR during the first 6 months post lung transplantation. HCMV viral loads were assessed in the PBL using an in-house quantitative HCMV PCR assay and the plasma using the COBAS Amplicor HCMV monitor test. HCMV disease in LTR was defined as histopathologically proven HCMV pneumonitis. Results: HCMV deoxyribonucleic acid (DNA) was detected in 39/98 (40%) of total samples with excellent agreement be, tween the two strategies. HCMV was detected in both the plasma and PBL in 38/39 (97%) of HCMV positive samples. HCMV viral loads were higher in patients with HCMV pneumonitis in both the PBL and plasma compared to patients without HCMV pneumonitis. Greater than 10-fold increases in HCMV DNA levels had a sensitivity of 88% and a specificity of 73% in the plasma for HCMV pneumonitis and a positive and negative predictive value of 70 and 89%, respectively. Greater that 10-fold increases in HCMV DNA levels in the PBL had a sensitivity of 88% and a specificity of 64%, for HCMV pneumonitis and a positive and negative predictive value of 64 and 88%, respectively. Conclusions: Acknowledging the difference in assay methods used for HCMV DNA quantitation, the in-house PCR PBL assay and the COBAS Amplicor HCMV monitor plasma assay predicted equally well HCMV pneumonitis in LTR. (C) 2002 Elsevier Science B.V. All rights reserved.
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页码:111 / 120
页数:10
相关论文
共 25 条
[1]   Early effects of ganciclovir therapy on the quantity of cytomegalovirus DNA in leukocytes of immunocompromised patients [J].
Boivin, G ;
Quirk, MR ;
Kringstad, BA ;
Germain, M ;
Jordan, MC .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (04) :860-862
[2]   Comparative evaluation of the cytomegalovirus DNA load in polymorphonuclear leukocytes and plasma of human immunodeficiency virus-infected subjects [J].
Boivin, G ;
Handfield, J ;
Toma, E ;
Murray, G ;
Lalonde, R ;
Bergeron, MG .
JOURNAL OF INFECTIOUS DISEASES, 1998, 177 (02) :355-360
[3]   Quantitative analysis of cytomegalovirus (CMV) viremia using the pp65 antigenemia assay and the COBAS AMPLICOR CMV MONITOR PCR test after blood and marrow allogeneic transplantation [J].
Boivin, G ;
Bélanger, R ;
Delage, R ;
Béliveau, C ;
Demers, C ;
Goyette, N ;
Roy, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (12) :4356-4360
[4]   Usefulness of the cytomegalovirus (CMV) antigenemia assay for predicting the occurrence of CMV disease and death in patients with AIDS [J].
Chevret, S ;
Scieux, C ;
Garrait, V ;
Dahel, L ;
Morinet, F ;
Modaï, J ;
Decazes, JM ;
Molina, JM .
CLINICAL INFECTIOUS DISEASES, 1999, 28 (04) :758-763
[5]   HUMAN HERPESVIRUS-6 IN LUNG-TISSUE FROM PATIENTS WITH PNEUMONITIS AFTER BONE-MARROW TRANSPLANTATION [J].
CONE, RW ;
HACKMAN, RC ;
HUANG, MLW ;
BOWDEN, RA ;
MEYERS, JD ;
METCALF, M ;
ZEH, J ;
ASHLEY, R ;
COREY, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 329 (03) :156-161
[6]   Application of viral-load kinetics to identify patients who develop cytomegalovirus disease after transplantation [J].
Emery, VC ;
Sabin, CA ;
Cope, AV ;
Gor, D ;
Hassan-Walker, AF ;
Griffiths, PD .
LANCET, 2000, 355 (9220) :2032-2036
[7]   CYTOMEGALOVIRUS-INFECTION AND PNEUMONITIS - IMPACT AFTER ISOLATED LUNG TRANSPLANTATION [J].
ETTINGER, NA ;
BAILEY, TC ;
TRULOCK, EP ;
STORCH, GA ;
ANDERSON, D ;
RAAB, S ;
SPITZNAGEL, EL ;
DRESLER, C ;
COOPER, JD .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1993, 147 (04) :1017-1023
[8]   Differences between the quantitative antigenemia assay and the COBAS Amplicor Monitor quantitative PCR assay for detecting CMV viraemia in bone marrow and solid organ transplant patients [J].
Flexman, J ;
Kay, I ;
Fonte, R ;
Herrmann, R ;
Gabbay, E ;
Palladino, S .
JOURNAL OF MEDICAL VIROLOGY, 2001, 64 (03) :275-282
[9]  
FLINT A, 1994, J HEART LUNG TRANSPL, V13, P38
[10]   Longitudinal fluctuations in cytomegalovirus load in bone marrow transplant patients: relationship between peak virus load, donor/recipient serostatus, acute GVHD and CMV disease [J].
Gor, D ;
Sabin, C ;
Prentice, HG ;
Vyas, N ;
Man, S ;
Griffiths, PD ;
Emery, VC .
BONE MARROW TRANSPLANTATION, 1998, 21 (06) :597-605