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Updated: Jan 10, 2026

Isolation and Transplantation of Different Aged Murine Thymic Grafts.
Published on: May 13, 2015
Transfer of Aging: Implications for Pediatric Solid Organ Transplantation
Rosalie Wolff von Gudenberg1,2, Lucas Said Josef Eckholt3,4, Simon Moosburner5
1Division of Transplant Surgery, Department of Surgery, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Insights
Older donor organs in pediatric transplants may transfer cellular senescence, accelerating aging and impairing outcomes. Senolytic therapies show promise for improving results in young recipients.
Area of Science:
- Transplantation immunology
- Gerontology
- Pediatric medicine
Background:
- Solid organ transplantation (SOT) is crucial for pediatric end-stage organ failure.
- Limited pediatric donor organs lead to increased use of older, age-mismatched donor organs.
- Older donor organs carry risks of heightened immunogenicity, rejection, and poorer long-term outcomes.
Purpose of the Study:
- To review the role of cellular senescence in pediatric organ transplantation.
- To discuss the potential transfer of senescence from aged donor organs to pediatric recipients.
- To explore strategies for mitigating the impact of senescence in pediatric transplant recipients.
Main Methods:
- Review of emerging evidence on cellular senescence in aged donor organs.
- Analysis of animal models demonstrating senescence transfer and its effects.
- Discussion of potential therapeutic interventions targeting senescence.
Main Results:
- Aged donor organs may transfer senescence, accelerating aging-like processes (frailty, cognitive decline, organ dysfunction) in pediatric recipients.
- Senescence induction could exacerbate pediatric conditions like chronic kidney disease and juvenile idiopathic arthritis.
- Animal studies confirm that older donor organs induce immune dysfunction and impairments in young recipients.
Conclusions:
- Cellular senescence is a significant factor in pediatric organ transplantation outcomes.
- Senolytic therapies represent a promising strategy to improve outcomes for pediatric recipients of aged donor organs.
- Further human studies are essential to validate findings and guide clinical practice, balancing donor pool expansion with age-matched transplantation.
Abstract:
Solid organ transplantation (SOT) is a life-saving intervention for pediatric patients with end-stage organ failure. Due to the limited availability of pediatric donor organs, organs from older donors are frequently utilized, increasing the risk of age-mismatched transplants. Older donor organs are linked to heightened immunogenicity, rejection rates, and impaired long-term outcomes. Emerging evidence suggests that aged donor organs may transfer senescence to pediatric recipients, accelerating aging-like processes such as frailty, cognitive decline, and organ dysfunction. Additionally, the induction of senescence could alter pediatric conditions like chronic kidney disease (CKD), juvenile idiopathic arthritis (JIA), and pediatric brain tumors which have been linked to augmented senescence. Animal models have shown that older donor organs induce senescence-associated changes in young recipients, including immune dysfunction and physical and cognitive impairments. This review highlights the role of cellular senescence in pediatric organ transplantation and discusses strategies to mitigate its impact. Therapies targeting senescence, such as senolytics, offer a potential approach to improve outcomes in pediatric recipients. Further research is needed to validate these findings in human studies and guide clinical strategies that expand the donor pool while prioritizing age-matched transplantation for pediatric patients.
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