Cytomegalovirus infection in solid organ transplant recipients: new challenges and their implications for preventive strategies
- PMID: 16406798
- DOI: 10.1016/j.jcv.2005.10.014
Cytomegalovirus infection in solid organ transplant recipients: new challenges and their implications for preventive strategies
Abstract
Background: Late-onset CMV disease is being increasingly recognized as a significant post-transplantation complication.
Objectives: To discern the impact of antiviral prophylactic strategies on the emerging syndrome of late-onset CMV disease in organ transplant recipients.
Study design: Review of existing reports and published data relevant to antiviral prophylaxis in organ transplant recipients.
Results: Prevention of CMV using prophylaxis has proven effective and is widely employed in organ transplant recipients. However, late-onset CMV disease is increasingly being recognized as a significant complication in these patients. The more potent the activity of the antiviral drug and the longer duration of prophylaxis, the greater likelihood of late-onset CMV disease. CMV seronegative recipients of seropositive donor allografts appear to be at a uniquely high risk. A higher proportion of patients with late-onset CMV have tissue invasive disease. Late-onset CMV disease in liver transplant recipients conferred an independently higher risk of mortality in the first post-transplant year. Prolonged antiviral therapy may impair the recovery of CMV-specific T-cell responses. Preemptive therapy appears to be less likely to be associated with CMV disease.
Conclusions: Discernment of the pathophysiologic basis of late-onset CMV warrants investigation. Preemptive therapy may be the preferable approach to CMV prophylaxis.
Similar articles
-
Improving outcomes for solid-organ transplant recipients at risk from cytomegalovirus infection: late-onset disease and indirect consequences.Clin Infect Dis. 2008 Mar 1;46(5):732-40. doi: 10.1086/527397. Clin Infect Dis. 2008. PMID: 18220478 Review.
-
Evaluation of cytomegalovirus (CMV)-specific T cell immune reconstitution revealed that baseline antiviral immunity, prophylaxis, or preemptive therapy but not antithymocyte globulin treatment contribute to CMV-specific T cell reconstitution in kidney transplant recipients.J Infect Dis. 2010 Aug 15;202(4):585-94. doi: 10.1086/654931. J Infect Dis. 2010. PMID: 20594105
-
Preemptive therapy versus universal prophylaxis with ganciclovir for cytomegalovirus in solid organ transplant recipients.Clin Infect Dis. 2001 Mar 1;32(5):742-51. doi: 10.1086/319225. Epub 2001 Feb 20. Clin Infect Dis. 2001. PMID: 11229841 Review.
-
Antiviral resistance in cytomegalovirus: an emerging problem in organ transplant recipients.Semin Respir Infect. 2002 Dec;17(4):265-73. doi: 10.1053/srin.2002.36447. Semin Respir Infect. 2002. PMID: 12497543 Review.
-
Cytomegalovirus infection and disease in the new era of immunosuppression following solid organ transplantation.Transpl Infect Dis. 2009 Jun;11(3):195-202. doi: 10.1111/j.1399-3062.2009.00372.x. Epub 2009 Feb 18. Transpl Infect Dis. 2009. PMID: 19228345 Review.
Cited by
-
Late-onset CMV disease following CMV prophylaxis.Ir J Med Sci. 2009 Sep;178(3):333-6. doi: 10.1007/s11845-009-0327-3. Epub 2009 Apr 2. Ir J Med Sci. 2009. PMID: 19340518
-
Current concepts on cytomegalovirus infection after liver transplantation.World J Hepatol. 2010 Sep 27;2(9):325-36. doi: 10.4254/wjh.v2.i9.325. World J Hepatol. 2010. PMID: 21161017 Free PMC article.
-
Rationally designed chemokine-based toxin targeting the viral G protein-coupled receptor US28 potently inhibits cytomegalovirus infection in vivo.Proc Natl Acad Sci U S A. 2015 Jul 7;112(27):8427-32. doi: 10.1073/pnas.1509392112. Epub 2015 Jun 15. Proc Natl Acad Sci U S A. 2015. PMID: 26080445 Free PMC article.
-
Restoring immune defenses via lymphotoxin signaling: lessons from cytomegalovirus.Immunol Res. 2006;34(3):243-54. doi: 10.1385/IR:34:3:243. Immunol Res. 2006. PMID: 16891674 Review.
-
Management of cytomegalovirus infection and disease in liver transplant recipients.World J Hepatol. 2014 Jun 27;6(6):370-83. doi: 10.4254/wjh.v6.i6.370. World J Hepatol. 2014. PMID: 25018848 Free PMC article. Review.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical