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Updated: Dec 22, 2025

Murine Cervical Heart Transplantation Model Using a Modified Cuff Technique
Published on: October 12, 2014
Impact of cytomegalovirus serologic status on heart transplantation
Alejandro Suarez-Pierre1, Katherine Giuliano1, Cecillia Lui1
1Department of Surgery, Johns Hopkins University, Baltimore, Maryland.
Insights
Cytomegalovirus (CMV) infection increases mortality risk after heart transplants, especially early on. Antiviral prophylaxis appears to reduce this risk, with no impact on allograft vasculopathy.
Area of Science:
- Cardiology
- Infectious Diseases
- Transplantation Immunology
Background:
- Cytomegalovirus (CMV) infection is a known risk factor for adverse outcomes post-heart transplant.
- Prior studies suggest CMV increases mortality, cardiac allograft vasculopathy, and malignancy risk.
- This study investigates the impact of recipient and donor CMV status on U.S. heart transplant recipients.
Purpose of the Study:
- To determine the association between cytomegalovirus (CMV) serologic status and long-term outcomes in adult heart transplant recipients.
- To evaluate the impact of CMV status on 5-year survival and cardiac allograft vasculopathy.
- To assess the effect of antiviral chemoprophylaxis on mortality risk in CMV-positive heart transplant recipients.
Main Methods:
- Analysis of adult heart transplant recipients from the OPTN registry (2005-2016).
- Stratification of recipients based on donor and recipient cytomegalovirus (CMV) serologic status.
- Cox proportional hazards regression models to assess associations between CMV status and 5-year survival and cardiac allograft vasculopathy.
Main Results:
- Five-year survival rates were similar across all cytomegalovirus (CMV) serologic groups (77-79%).
- CMV seropositivity was associated with a 23%-41% increased risk of mortality, particularly within the first 3 months post-transplant.
- Valganciclovir use significantly decreased mortality risk (HR 0.56; 95% CI, 0.52-0.60).
- Cardiac allograft vasculopathy incidence was similar across all CMV status groups (30-31%).
Conclusions:
- CMV seropositivity at heart transplantation is linked to an elevated long-term mortality risk.
- Antiviral chemoprophylaxis appears effective in mitigating the increased mortality risk associated with CMV.
- No significant association was found between CMV status and an increased risk of cardiac allograft vasculopathy.
Background:
Cytomegalovirus (CMV) infection has been associated with increased risk of mortality, cardiac allograft vasculopathy, and de novo malignancy following heart transplantation in prior institutional reports. This study examines the impact of the recipient and donor CMV status on heart recipients in the United States.
Methods:
Adult heart transplant recipients were identified in the OPTN registry between 2005-2016. Recipients were stratified based on the recipient (R) and donor (D) CMV serologic status (+/-). The primary endpoint was survival 5-years after transplantation. The secondary endpoint was cardiac allograft vasculopathy 5-years after transplantation. Separate Cox proportional hazards regression models were developed to evaluate independent associations between CMV status and each of the study endpoints.
Results:
A total of 21 878 recipients met the inclusion criteria. The breakdown of study arms by CMV serologic status was R-/D- = 3412, R+/D- = 4939; R-/D+ = 5230, and R+/D+ = 8,297. Five-year survival estimates were similar across groups (77-79%). CMV status was associated with increased mortality at 5-years (23%-41% increased risk) which was most evident in the first 3 months. The use of valganciclovir was associated with decreased risk of mortality (HR 0.56; 95% CI, 0.52-0.60). The cumulative incidence of cardiac allograft vasculopathy (R-/D- = 31%, R+/D- = 30%, R-/D+ = 31%, and R+/D+ = 30%) was similar across groups.
Conclusions:
CMV seropositivity at the time of transplantation is associated with increased long-term risk of mortality. Chemoprophylaxis with antivirals seems to mitigate this risk. There was no association with an increased risk of allograft vasculopathy.
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