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Published on: October 12, 2014
Cytomegalovirus Donor Seropositivity Negatively Affects Survival After Heart Transplantation
Christian Heim1, Philipp P Müller1, René Tandler1
1Department of Cardiac Surgery, University of Erlangen-Nuremberg, Erlangen, Germany.
Insights
Donor cytomegalovirus (CMV) positivity significantly reduces survival after heart transplantation (HTx). However, CMV status did not impact cardiac allograft vasculopathy (CAV) development in this study.
Area of Science:
- Immunology
- Transplantation Medicine
- Infectious Diseases
Background:
- Cytomegalovirus (CMV) infection is a known risk factor for cardiac allograft vasculopathy (CAV) and reduced long-term survival post-heart transplantation (HTx).
- Understanding the impact of different CMV donor:recipient serologic combinations is crucial for improving transplant outcomes.
Purpose of the Study:
- To compare posttransplant survival rates across various cytomegalovirus (CMV) donor:recipient serologic combinations.
- To evaluate the association between CMV serologic status and the development of cardiac allograft vasculopathy (CAV) after heart transplantation (HTx).
Main Methods:
- Retrospective cohort study of 15,885 adult primary heart transplant recipients.
- Analysis of data from the International Society for Heart and Lung Transplantation Thoracic Transplant Registry (July 2004-June 2014).
- Comparison of posttransplant survival and CAV risk among four CMV serologic groups: D+R-, D+R+, D-R+, and D-R-.
Main Results:
- Donor CMV positivity (D+) was associated with significantly worse short- and long-term survival compared to CMV-seronegative recipients (D-R-).
- Recipient CMV seropositivity alone (D-R+) did not significantly impact survival.
- The risk of developing cardiac allograft vasculopathy (CAV) was not significantly increased in CMV-positive donor groups (D+) compared to CMV-negative donor groups (D-).
Conclusions:
- Donor cytomegalovirus (CMV) seropositivity is linked to reduced survival after heart transplantation (HTx), but not CAV development.
- Strategies to mitigate the adverse effects of CMV on post-transplant survival are necessary.
Background:
Prior studies have shown that cytomegalovirus (CMV) infection is a risk factor for the development of cardiac allograft vasculopathy (CAV) and is associated with reduced long-term survival after heart transplantation (HTx). The aim of this International Society for Heart and Lung Transplantation Transplant Registry study was to compare posttransplant survival in different CMV donor:recipient serologic combinations.
Methods:
We performed a retrospective cohort study, using the International Society for Heart and Lung Transplantation Thoracic Transplant Registry, on 15 885 adult primary heart transplant recipients with known CMV serologic status between July 2004 and June 2014. Posttransplant survival and risk of developing CAV were compared across 4 groups: CMV-seronegative recipients (R-) receiving CMV-positive grafts (D+), intermediate-risk patients (D+R+ and D-R+), and low-risk patients (D-R-).
Results:
Baseline characteristics (donor/recipient age, body mass index, recipient serum creatinine, blood group, donor cause of death, recipient diagnosis, and ischemic time) were mostly balanced between the groups. Kaplan-Meier survival analyses over a follow-up of 10 y revealed significantly worse survival for both D+ groups as compared to the CMV low-risk group (D+R+: 56.61% [95% confidence interval, 53.94-59.41] versus D-R-: 63.09% [59.74-66.64] P < 0.01 and D+R-: 57.69% [56.03-59.39] versus D-R-; P < 0.001), whereas recipient seropositivity alone was not associated with reduced survival (D-R+ versus D-R-P = 0.178). The risk of developing CAV after HTx was not significantly increased in D+ as compared to D- groups.
Conclusions:
In a large contemporary cohort, CMV status at the time of HTx was not associated with CAV development. However, there was a significant association between donor CMV seropositivity and reduced short- and long-term survival after HTx. Approaches to mitigate the impact of CMV on posttransplant survival are needed.
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