Use of real-time PCR to measure Epstein-Barr virus genomes in whole blood

被引:18
作者
Leung, E
Shenton, BK
Jackson, G
Gould, FK
Yap, C
Talbot, D
机构
[1] Univ Newcastle Upon Tyne, Sch Med, Dept Surg, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
[2] Royal Victoria Infirm, Dept Haematol, Newcastle Upon Tyne NE1 4LP, Tyne & Wear, England
[3] Freeman Rd Hosp, Dept Microbiol, Newcastle Upon Tyne NE7 7DN, Tyne & Wear, England
[4] Univ Glasgow, Dept Stat, Glasgow G12 8QQ, Lanark, Scotland
[5] Freeman Rd Hosp, Dept Renal Transplantat, Newcastle Upon Tyne NE7 7DN, Tyne & Wear, England
关键词
EBV; PTLD; real-time PCR;
D O I
10.1016/S0022-1759(02)00333-2
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The measurement of the Epstein-Barr viral load in peripheral blood has been recognised as an important way of monitoring the response to treatment in patients with Epstein-Barr virus (EBV)-related malignancies. In particular, EBV load in transplant recipients can be used as a predictive parameter for Post-transplant Lymphoproliferative Disorder (PTLD). The aim was to develop a rapid and reliable PCR protocol for the quantification of the cell-associated EBV genome. Real-time PCR using TaqMan methodology was established. This technique was applied to determine the EBV load in various study groups including healthy controls, transplant recipients, patients on haemodialysis, and patients with infectious mononucleosis. The baseline level of EBV genomes in the immunosuppressed renal transplant recipients was significantly different from that in the healthy controls. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:259 / 267
页数:9
相关论文
共 39 条
[1]   EPSTEIN-BARR-ENCODED RNA IN-SITU HYBRIDIZATION - DIAGNOSTIC APPLICATIONS [J].
AMBINDER, RF ;
MANN, RB .
HUMAN PATHOLOGY, 1994, 25 (06) :602-605
[2]  
Bai X, 1997, CLIN CHEM, V43, P1843
[3]   High levels of Epstein-Barr virus DNA in blood of solid-organ transplant recipients and their value in predicting posttransplant lymphoproliferative disorders [J].
Baldanti, F ;
Grossi, P ;
Furione, M ;
Simoncini, L ;
Sarasini, A ;
Comoli, P ;
Maccario, R ;
Fiocchi, R ;
Gerna, G .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (02) :613-619
[4]  
Bolufer P, 2000, HAEMATOLOGICA, V85, P1248
[5]   Routine use of real-time quantitative PCR for laboratory diagnosis of Epstein-Barr virus infections [J].
Brengel-Pesce, K ;
Morand, P ;
Schmuck, A ;
Bourgeat, MJ ;
Buisson, M ;
Barguès, G ;
Bouzid, M ;
Seigneurin, JM .
JOURNAL OF MEDICAL VIROLOGY, 2002, 66 (03) :360-369
[6]  
Chadburn A, 1997, SEMIN DIAGN PATHOL, V14, P15
[7]   History and classification of human leukemia-lymphoma cell lines [J].
Drexler, HG ;
Minowada, J .
LEUKEMIA & LYMPHOMA, 1998, 31 (3-4) :305-316
[8]   Diagnosis of herpes simplex virus infections in the clinical laboratory by LightCycler PCR [J].
Espy, MJ ;
Uhl, JR ;
Mitchell, PS ;
Thorvilson, JN ;
Svien, KA ;
Wold, AD ;
Smith, TF .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (02) :795-799
[9]  
Gallagher A, 1999, INT J CANCER, V84, P442, DOI 10.1002/(SICI)1097-0215(19990820)84:4<442::AID-IJC20>3.3.CO
[10]  
2-A