Clinical trial of quantitative real-time polymerase chain reaction for detection of cytomegalovirus in peripheral blood of allogeneic hematopoietic stem-cell transplant recipients

被引:44
作者
Cortez, KJ
Fischer, SH
Fahle, GA
Calhoun, LB
Childs, RW
Barrett, AJ
Bennett, JE
机构
[1] NIAID, Clin Mycol Sect, Clin Invest Lab, NIH, Bethesda, MD 20892 USA
[2] NHLBI, Microbiol Serv, Dept Lab Med, Warren Grant Magnuson Clin Ctr,NIH, Bethesda, MD 20892 USA
[3] NHLBI, Stem Cell Allotransplant Unit, Hematol Branch, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1086/378413
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The preemptive therapy of cytomegalovirus (CMV) reactivation is useful for the prevention of CMV disease in allogeneic hematopoietic stem-cell transplant (HSCT) recipients. We compared results of the pp65 CMV antigenemia test with quantitative touch-down polymerase chain reaction (Q-PCR) on unfractionated whole blood for the detection of CMV reactivation in 51 HSCT recipients. Forty episodes of reactivation in 28 patients were detected by antigenemia and treated by antiviral drugs. Q-PCR detected CMV DNA in 39 (97.5%) of 40 reactivation episodes. False-positive results occurred in 3% of tests, of which 63% were borderline positive. Q-PCR results were positive earlier than antigenemia results in 30 (77%) of 39 episodes detected by antigenemia. Q-PCR remained positive after treatment was discontinued in 14 (36%) of 39 episodes and predicted the return of CMV reactivation in 4 (31%) of 13 episodes. Q-PCR was more sensitive than the antigenemia test and had sufficient specificity for clinical use.
引用
收藏
页码:967 / 972
页数:6
相关论文
共 12 条
[1]   Successful modification of a pp65 antigenemia-based early treatment strategy for prevention of cytomegalovirus disease in allogeneic marrow transplant recipients [J].
Boeckh, M ;
Bowden, RA ;
Gooley, T ;
Myerson, D ;
Corey, L .
BLOOD, 1999, 93 (05) :1781-1782
[2]   Cytomegalovirus pp65 antigenemia-guided early treatment with ganciclovir versus ganciclovir at engraftment after allogeneic marrow transplantation: A randomized double-blind study [J].
Boeckh, M ;
Gooley, TA ;
Myerson, D ;
Cunningham, T ;
Schoch, G ;
Bowden, RA .
BLOOD, 1996, 88 (10) :4063-4071
[3]   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
[4]   Comparison of six commercial DNA extraction kits for recovery of cytomegalovirus DNA from spiked human specimens [J].
Fahle, GA ;
Fischer, SH .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (10) :3860-3863
[5]   EARLY TREATMENT WITH GANCICLOVIR TO PREVENT CYTOMEGALOVIRUS DISEASE AFTER ALLOGENEIC BONE-MARROW TRANSPLANTATION [J].
GOODRICH, JM ;
MORI, M ;
GLEAVES, CA ;
DUMOND, C ;
CAYS, M ;
EBELING, DF ;
BUHLES, WC ;
DEARMOND, B ;
MEYERS, JD .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (23) :1601-1607
[6]   Improved monitoring of cytomegalovirus infection after allogeneic hematopoietic stem cell transplantation by an ultrasensitive plasma DNA PCR assay [J].
Kaiser, L ;
Perrin, L ;
Chapuis, B ;
Hadaya, K ;
Kolarova, L ;
Deffernez, C ;
Huguet, S ;
Helg, C ;
Wunderli, W .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (11) :4251-4255
[7]   Development and evaluation of a quantitative, touch-down, real-time PCR assay for diagnosing Pneumocystis carinii pneumonia [J].
Larsen, HH ;
Masur, H ;
Kovacs, JA ;
Gill, VJ ;
Silcott, VA ;
Kogulan, P ;
Maenza, J ;
Smith, M ;
Lucey, DR ;
Fischer, SH .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (02) :490-494
[8]   The clinical use of various blood compartments for cytomegalovirus (CMV) DNA quantitation in transplant recipients with CMV disease [J].
Razonable, RR ;
Brown, RA ;
Wilson, J ;
Groettum, C ;
Kremers, W ;
Espy, M ;
Smith, TF ;
Paya, CV .
TRANSPLANTATION, 2002, 73 (06) :968-973
[9]   Cytomegalovirus (CMV) DNA load predicts relapsing CMV infection after solid organ transplantation [J].
Sia, IG ;
Wilson, JA ;
Groettum, CM ;
Espy, MJ ;
Smith, TF ;
Paya, CV .
JOURNAL OF INFECTIOUS DISEASES, 2000, 181 (02) :717-720
[10]   Continuous fluorescence monitoring of rapid cycle DNA amplification [J].
Wittwer, CT ;
Herrmann, MG ;
Moss, AA ;
Rasmussen, RP .
BIOTECHNIQUES, 1997, 22 (01) :130-&