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Published on: May 8, 2020
Outcome of patients having heart transplantation for lymphocytic myocarditis
Saeko Yoshizawa1, Tomoko Sugiyama Kato, Donna Mancini
1Department of Pathology and Cell Biology, Columbia University Medical Center and The New York Presbyterian Hospital, New York, NY, USA. saeko0804@gmail.com
Insights
Patients undergoing heart transplantation (HT) for lymphocytic myocarditis (LM) experience similar long-term survival rates compared to those with idiopathic dilated cardiomyopathy or ischemic cardiomyopathy. However, LM patients show a higher incidence of late acute cellular rejection (ACR) after HT.
Area of Science:
- Cardiology
- Transplantation Immunology
- Pathology
Background:
- Heart transplantation (HT) for myocarditis remains controversial due to historical concerns about post-procedural prognosis.
- Assessing the impact of lymphocytic myocarditis (LM) on cardiac allograft rejection and survival in the current era of HT is crucial.
Purpose of the Study:
- To evaluate if lymphocytic myocarditis (LM) in explanted hearts influences cardiac allograft rejection and survival post-heart transplantation (HT).
- To compare outcomes of HT patients with LM against those with idiopathic dilated cardiomyopathy (IDC) and ischemic cardiomyopathy (IC).
Main Methods:
- Retrospective review of 759 consecutive de novo HT patients (2000-2010).
- Comparison of prognosis between patients with pathologically proven LM (n=32) and matched IDC (n=96) and IC (n=64) groups.
- Analysis of biopsy-diagnosed acute cellular rejection (ACR) and antibody-mediated rejection, alongside posttransplant survival rates.
Main Results:
- No significant difference in first-year acute cellular rejection (ACR) events among the three groups.
- Increased frequency of late ACR (after the first year) observed in the LM group compared to the IC group (3.8% vs. 0.5%, p=0.006).
- No significant differences in antibody-mediated rejection or overall posttransplant survival among the LM, IDC, and IC groups.
Conclusions:
- Patients with pre-HT LM exhibit a higher rate of late ACR post-transplantation compared to those with IC.
- Long-term survival after HT for LM is comparable to that for IDC and IC, suggesting HT is a viable option.
- LM should be considered in pre-transplant evaluations, with awareness of potential late rejection episodes.
Abstract:
Heart transplantation (HT) for myocarditis has been controversial because of earlier reports of a poor prognosis after the procedure. We sought to determine whether lymphocytic myocarditis (LM) at the time of HT affects cardiac allograft rejection and survival after HT compared with other patients without LM in the current era of HT. We retrospectively reviewed 759 consecutive patients who underwent de novo HT at Columbia University Medical Center between 2000 and 2010 and compared prognosis after HT of the patients with pathologically proven LM in their explanted hearts with that of age- and gender-matched patients with idiopathic dilated cardiomyopathy (IDC group; n = 96) and with ischemic cardiomyopathy (IC group; n = 64). Thirty-two patients (4.2%) had LM in the explanted hearts pathologically. Among the 3 groups, no statistically significant difference was observed in the number of biopsy-diagnosed acute cellular rejection (ACR; International Society for Heart & Lung Transportation grade ≥2R) events during the first year after HT. In contrast, the frequency of biopsy-diagnosed ACR in subsequent years was greater in the LM group (n = 8, 3.8%) than in IC group (n = 3, 0.5%, p = 0.006), although no different from that of patients with IDC. The frequency of antibody-mediated rejection and posttransplant survival did not differ among the 3 groups. In conclusion, patients with pre-HT LM have an increased frequency of late ACR after HT compared with patients with IC. Nevertheless, survival of LM patients after HT is comparable to that of patients transplanted for IDC or IC.
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