Prophylaxis for CMV should not now replace pre-emptive therapy in solid organ transplantation

被引:72
作者
Emery, VC [1 ]
机构
[1] UCL Royal Free & Univ Coll Med Sch, Dept Virol, London NW3 2QG, England
关键词
D O I
10.1002/rmv.310
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Pre-emptive therapy (PET) initiated on the basis of HCMV positivity in the blood using sensitive methods such as PCR, nucleic acid sequence based amplification or antigenaemia offers several advantages for the management of HCMV infection. These include the ability to target antiviral drug therapy to those most at risk of future disease, minimising drug exposure and maximising cost-benefit. In addition, allowing limited replication to occur also provides immune stimulation which will be important for future control of HCMV replication. In contrast, prophylaxis is a high-cost strategy which exposes all patients to potentially toxic drugs, does not facilitate immune priming and leads to the development of late HCMV infection and disease in high-risk patients. Copyright (C) 2001 John Wiley & Sons, Ltd.
引用
收藏
页码:83 / 86
页数:4
相关论文
共 22 条
[1]   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
[2]   Cytomegalovirus polymerase chain reaction viraemia in patients receiving ganciclovir maintenance therapy for retinitis [J].
Bowen, EF ;
Emery, VC ;
Wilson, P ;
Johnson, MA ;
Davey, CC ;
Sabin, CA ;
Farmer, D ;
Griffiths, PD .
AIDS, 1998, 12 (06) :605-611
[3]   Prediction of cytomegalovirus load and resistance patterns after antiviral chemotherapy [J].
Emery, VC ;
Griffiths, PD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (14) :8039-8044
[4]   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
[5]   The dynamics of human cytomegalovirus replication in vivo [J].
Emery, VC ;
Cope, AV ;
Bowen, EF ;
Gor, D ;
Griffiths, PD .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 190 (02) :177-182
[6]   Viral dynamics during active cytomegalovirus infection and pathology [J].
Emery, VC .
INTERVIROLOGY, 1999, 42 (5-6) :405-411
[7]   Randomised trial of efficacy and safety of oral ganciclovir in the prevention of cytomegalovirus disease in liver-transplant recipients [J].
Gane, E ;
Saliba, F ;
Valdecasas, GJC ;
OGrady, J ;
Pescovitz, MD ;
Lyman, S ;
Robinson, CA .
LANCET, 1997, 350 (9093) :1729-1733
[8]  
GRIFFITHS PD, 1997, CLIN VIROLOGY, P445
[9]   Cytomegalovirus monitoring by polymerase chain reaction of whole blood samples from patients undergoing autologous bone marrow or peripheral blood progenitor cell transplantation [J].
Hebart, H ;
Schroder, A ;
Loffler, J ;
Klingebiel, T ;
Martin, H ;
Wassmann, B ;
Gerneth, F ;
Rabenau, H ;
Jahn, G ;
Kanz, L ;
Muller, CA ;
Einsele, H .
JOURNAL OF INFECTIOUS DISEASES, 1997, 175 (06) :1490-1493
[10]   Clinical utility of quantitative cytomegalovirus viral load determination for predicting cytomegalovirus disease in liver transplant recipients [J].
Humar, A ;
Gregson, D ;
Caliendo, AM ;
McGeer, A ;
Malkan, G ;
Krajden, M ;
Corey, P ;
Greig, P ;
Walmsley, S ;
Levy, G ;
Mazzulli, T .
TRANSPLANTATION, 1999, 68 (09) :1305-1311