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Updated: May 22, 2026

Expanding Cytotoxic T Lymphocytes from Umbilical Cord Blood that Target Cytomegalovirus, Epstein-Barr Virus, and Adenovirus
Published on: May 7, 2012
Immune response to CMV in solid organ transplant recipients: current concepts and future directions
Richard R Watkins1, Tracy L Lemonovich, Raymund R Razonable
1Division of Infectious Diseases, Akron General Medical Center, 224 W. Exchange Street, Akron, OH 44302, USA. rwatkins@agmc.org
Abstract:
Despite advances in immunosuppression and antiviral therapy, CMV continues to be a significant opportunistic pathogen adversely affecting the outcome of solid organ transplantation (SOT) recipients. While a significant proportion of CMV disease is caused by reactivation of latent virus, the risk is highest among CMV donor+ and recipient- SOT patients. CMV is responsible for both direct (e.g., pneumonitis, colitis) and indirect (e.g., rejection, atherosclerosis) morbidity and mortality. Healthy CMV-seropositive individuals have a high frequency of CMV-specific CD4(+) and CD8(+) T cells that provide immune protection by limiting CMV reactivation and replication. Changes to the innate and adaptive immune system from immunosuppressive therapy following SOT contribute to CMV disease pathogenesis. CMV disease after SOT is associated with poorer outcomes, thus novel strategies to prevent it are an area of active research. In this article, we review the current state of knowledge on the immune response to CMV following SOT.
Insights
Cytomegalovirus (CMV) remains a threat in solid organ transplantation (SOT). Understanding the immune response to CMV post-SOT is crucial for developing novel prevention strategies against this opportunistic pathogen.
Area of Science:
- Immunology
- Transplantation Medicine
- Virology
Background:
- Cytomegalovirus (CMV) is a significant opportunistic pathogen impacting solid organ transplantation (SOT) outcomes.
- CMV disease, often due to viral reactivation, poses the highest risk in CMV donor-positive and recipient-negative SOT patients.
- CMV contributes to both direct (e.g., pneumonitis, colitis) and indirect (e.g., rejection, atherosclerosis) complications.
Purpose of the Study:
- To review the current understanding of the immune response to CMV in SOT recipients.
- To highlight the role of T cells in controlling CMV reactivation and replication.
- To discuss how immunosuppressive therapy affects immune responses and contributes to CMV disease pathogenesis.
Main Methods:
- Review of existing literature on CMV immunology and SOT.
- Analysis of immune system changes (innate and adaptive) following SOT.
- Examination of CMV-specific CD4(+) and CD8(+) T cell functions.
Main Results:
- Healthy CMV-seropositive individuals possess protective CMV-specific T cells.
- Immunosuppressive therapy after SOT alters immune defenses, increasing CMV disease risk.
- CMV disease in SOT recipients is linked to adverse outcomes.
Conclusions:
- CMV remains a critical challenge in SOT, necessitating further research.
- Novel strategies for CMV prevention in SOT are actively being investigated.
- A comprehensive understanding of the immune response is key to mitigating CMV's impact.
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