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Updated: Jun 23, 2026

Tissue Engineering of the Intestine in a Murine Model
Published on: December 1, 2012
Current perspectives on pediatric intestinal transplantation
George V Mazariegos1, Robert H Squires, Rakesh K Sindhi
1Children's Hospital of Pittsburgh, Pittsburgh, PA 15213, USA. george.mazariegos@chp.edu
Insights
Pediatric intestinal failure, often from surgical issues or motility disorders, may necessitate intestine transplantation. Centers of excellence report high survival rates, with research focused on reducing chronic rejection.
Area of Science:
- Pediatric surgery
- Gastroenterology
- Transplantation immunology
Background:
- Pediatric intestinal failure stems from surgical conditions (e.g., necrotizing enterocolitis, gastroschisis) or functional disorders (e.g., intestinal pseudo-obstruction, microvillus inclusion disease).
- Intestine replacement becomes necessary for severe cases impacting growth and quality of life.
Purpose of the Study:
- To outline the indications, surgical approaches, immunosuppression protocols, and outcomes of intestinal transplantation in children.
- To highlight the current survival rates and future research directions in pediatric intestinal transplantation.
Main Methods:
- Review of indications for intestinal transplantation, including liver dysfunction, central line complications, and severe dehydration.
- Description of surgical techniques: isolated intestine, combined liver-intestine, and multivisceral transplantation.
- Summary of immunosuppression regimens, primarily tacrolimus-based with induction therapy.
Main Results:
- Centers of excellence report 1-year patient survival rates of 95% and 5-year survival rates of 77%.
- Key indications include liver dysfunction, loss of venous access, and recurrent sepsis or dehydration.
Conclusions:
- Intestinal transplantation is a viable option for children with irreversible intestinal failure, offering significant survival benefits.
- Ongoing research aims to mitigate long-term graft loss, particularly from chronic rejection, to further improve patient outcomes.
Abstract:
Irreversible intestinal failure in children is predominantly caused by surgical conditions such as volvulus, necrotizing enterocolitis, and gastroschisis. Functional intestinal failure from motility disorders such as intestinal pseudo-obstruction or enterocyte dysfunction with microvillus inclusion disease also may require intestine replacement. Approved indications for intestinal transplantation include liver dysfunction, loss of major venous access, frequent central line-related sepsis, and recurrent episodes of severe dehydration despite intravenous fluid management. Surgical options include transplantation of the isolated intestine, combined liver-intestine transplantation, or multivisceral transplantation of the stomach, duodenum, pancreas, and small bowel (with or without the liver). Immunosuppression for intestinal transplantation is based on tacrolimus therapy, often with induction immunosuppression using antilymphocyte antibodies (eg, antithymocyte antibody and alemtuzumab). Experience at centers of excellence demonstrates 1- and 5-year patient survival rates of 95% and 77%, respectively, with ongoing investigations focusing on lowering long-term causes of graft loss such as chronic rejection.
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