Improving outcomes for solid-organ transplant recipients at risk from cytomegalovirus infection: Late-onset disease and indirect consequences

被引:73
作者
Legendre, Christophe [1 ]
Pascual, Manuel [2 ]
机构
[1] Hop Necker Enfants Malad, Serv Transplantat Renale, F-75015 Paris, France
[2] CHU Vaudois, Transplantat Ctr, CH-1011 Lausanne, Switzerland
关键词
D O I
10.1086/527397
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cytomegalovirus (CMV) is one of the most important pathogens following solid-organ transplantation, and effective prevention of CMV infection is a priority. The long-term control of CMV infection is dependent, in part, on the development of CMV-specific T cells, and controversy exists regarding whether CMV prophylaxis may prevent this. Although preemptive therapy is beneficial for the prevention of CMV disease, monitoring of viral levels in the blood does not always reflect what is occurring in tissues. Persistent low-level CMV infection has been associated with indirect consequences, such as transplant-associated vasculopathy, posttransplantation diabetes, an increased risk of opportunistic infection, and graft rejection. The issues surrounding preventive strategies for CMV disease following solid-organ transplantation are reviewed. We argue that prophylaxis is more effective than preemptive therapy; extending the duration of prophylaxis to the period of less intense immunosuppression could protect patients from late-onset disease, as well as from the indirect effects of CMV infection.
引用
收藏
页码:732 / 740
页数:9
相关论文
共 80 条
[51]  
Razonable Raymund R, 2004, Herpes, V11, P77
[52]  
Razonable RR, 2005, J INFECT DIS, V192, P1331, DOI [10.1086/466529, 10.1086/466532]
[53]   Dynamics of cytomegalovirus replication during preemptive therapy with oral ganciclovir [J].
Razonable, RR ;
van Cruijsen, H ;
Brown, RA ;
Wilson, JA ;
Harmsen, WS ;
Wiesner, RH ;
Smith, TF ;
Paya, CV .
JOURNAL OF INFECTIOUS DISEASES, 2003, 187 (11) :1801-1808
[54]   Modelling cytomegalovirus replication patterns in the human host: factors important for pathogenesis [J].
Regoes, Roland R. ;
Bowen, E. Frances ;
Cope, Alethea V. ;
Gor, Dehila ;
Hassan-Walker, Aycan F. ;
Prentice, H. Grant ;
Johnson, Margaret A. ;
Sweny, Paul ;
Burroughs, Andrew K. ;
Griffiths, Paul D. ;
Bonhoeffer, Sebastian ;
Emery, Vincent C. .
PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2006, 273 (1596) :1961-1967
[55]   Development of virus-specific CD4+ T cells during primary cytomegalovirus infection [J].
Rentenaar, RJ ;
Gamadia, LE ;
van der Hoek, N ;
van Diepen, FNJ ;
Boom, R ;
Weel, JFL ;
Wertheim-van Dillen, PME ;
van Lier, RAW ;
ten Berge, IJM .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 105 (04) :541-548
[56]   Cytomegalovirus (CMV)-specific T cell immunity after renal transplantation mediates protection from CMV disease by limiting the systemic virus load [J].
Reusser, P ;
Cathomas, G ;
Attenhofer, R ;
Tamm, M ;
Thiel, G .
JOURNAL OF INFECTIOUS DISEASES, 1999, 180 (02) :247-253
[57]  
RUBIN RH, 1989, JAMA-J AM MED ASSOC, V261, P3607
[58]   Impact of early cytomegalovirus infection and disease on long-term recipient and kidney graft survival [J].
Sagedal, S ;
Hartmann, A ;
Nordal, KP ;
Osnes, K ;
Leivestad, T ;
Foss, A ;
Degré, M ;
Fauchald, P ;
Rollag, H .
KIDNEY INTERNATIONAL, 2004, 66 (01) :329-337
[59]  
Schäfer P, 2001, J MED VIROL, V65, P85, DOI 10.1002/jmv.2005
[60]   Efficacy of valganciclovir administered as preemptive therapy for cytomegalovirus disease in liver transplant recipients: Impact on viral load and late-onset cytomegalovirus disease [J].
Singh, N ;
Wannstedt, C ;
Keyes, L ;
Gayowski, T ;
Wagener, MM ;
Gacciarelli, TV .
TRANSPLANTATION, 2005, 79 (01) :85-90