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Published on: May 27, 2011
Successful conversion to everolimus after cytomegalovirus infection in a heart transplant recipient
Teruhiko Imamura1, Taro Shiga, Koichiro Kinugawa
1Department of Cardiovascular Medicine, Graduate School of Medicine, The University of Tokyo, Japan.
Insights
Cytomegalovirus infection is a risk after heart transplants. Everolimus (EVL) may prevent cytomegalovirus (CMV) reactivation and neutropenia, offering a safer alternative to valganciclovir (VGC) and mycophenolate mofetil (MMF).
Area of Science:
- Immunology
- Transplantation Medicine
- Infectious Diseases
Background:
- Cytomegalovirus (CMV) infection is a significant threat in heart transplant recipients, contributing to cardiac allograft vasculopathy and mortality.
- Valganciclovir (VGC), a common treatment for CMV, is frequently associated with neutropenia, particularly when co-administered with mycophenolate mofetil (MMF).
Observation:
- A heart transplant recipient experiencing CMV antigenemia and progressive neutropenia while on VGC and MMF.
- Switching mycophenolate mofetil (MMF) to everolimus (EVL) resulted in sustained negative CMV antigenemia assays, even after VGC discontinuation.
- In a cohort of 14 heart transplant recipients, everolimus (EVL) administration was associated with consistently negative CMV antigenemia assays.
Findings:
- Everolimus (EVL) demonstrated a potential prophylactic effect against cytomegalovirus (CMV) reactivation in heart transplant recipients.
- The switch from MMF to EVL successfully managed CMV antigenemia and resolved neutropenia in the observed case.
- Everolimus (EVL) appears to be a viable alternative for managing or preventing CMV infection and associated complications in heart transplant patients.
Implications:
- Everolimus (EVL) may serve as a crucial alternative immunosuppressant to mitigate CMV-related complications and neutropenia in heart transplant recipients.
- Early consideration of everolimus (EVL) in CMV-seronegative heart transplant recipients could be beneficial for prophylaxis.
- This finding suggests a potential shift in immunosuppressive strategies to improve outcomes in heart transplantation.
Abstract:
Cytomegalovirus (CMV) infection remains a major problem in recipients with heart transplantation (HTx), because it may play a significant role in the development of cardiac allograft vasculopathy, which is one of the major causes of death after HTx. Valganciclovir (VGC) is effective for the treatment of CMV infection, but is often associated with neutropenia, especially when used with mycophenolate mophetil (MMF). We experienced an HTx recipient with positive CMV antigenemia who suffered progressive neutropenia after administration of VGC. We switched MMF to everolimus (EVL) and assay for CMV antigenemia was constantly negative even after discontinuation of VGC. In all other 14 HTx recipients who received EVL for any reason, we found that assay for CMV antigenemia remained negative throughout the period of EVL administration. Considering the prophylactic effect on CMV, EVL can not only be an alternative to rescue from comorbidity, but might also be indicated earlier especially in CMV-seronegative HTx recipients.
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