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Tissue engineering for the treatment of short bowel syndrome in children

Short bowel syndrome is a major cause of morbidity and mortality in children. Despite decades of experience in the management of short bowel syndrome, current therapy is primarily supportive. Definitive treatment often requires intestinal transplantation, which is associated with significant morbidi...

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Autores principales: Martin, Laura Y., Ladd, Mitchell R., Werts, Adam, Sodhi, Chhinder P., March, John C., Hackam, David J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6002962/
https://www.ncbi.nlm.nih.gov/pubmed/28937976
http://dx.doi.org/10.1038/pr.2017.234
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author Martin, Laura Y.
Ladd, Mitchell R.
Werts, Adam
Sodhi, Chhinder P.
March, John C.
Hackam, David J.
author_facet Martin, Laura Y.
Ladd, Mitchell R.
Werts, Adam
Sodhi, Chhinder P.
March, John C.
Hackam, David J.
author_sort Martin, Laura Y.
collection PubMed
description Short bowel syndrome is a major cause of morbidity and mortality in children. Despite decades of experience in the management of short bowel syndrome, current therapy is primarily supportive. Definitive treatment often requires intestinal transplantation, which is associated with significant morbidity and mortality. In order to develop novel approaches to the treatment of short bowel syndrome, we and others have focused on the development of an artificial intestine, by placing intestinal stem cells on a bioscaffold that has an absorptive surface resembling native intestine, and taking advantage of neovascularization to develop a blood supply. This review will explore recent advances in biomaterials, vascularization, and progress towards development of a functional epithelium and mesenchymal niche, highlighting both success and ongoing challenges in the field.
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spelling pubmed-60029622018-06-15 Tissue engineering for the treatment of short bowel syndrome in children Martin, Laura Y. Ladd, Mitchell R. Werts, Adam Sodhi, Chhinder P. March, John C. Hackam, David J. Pediatr Res Article Short bowel syndrome is a major cause of morbidity and mortality in children. Despite decades of experience in the management of short bowel syndrome, current therapy is primarily supportive. Definitive treatment often requires intestinal transplantation, which is associated with significant morbidity and mortality. In order to develop novel approaches to the treatment of short bowel syndrome, we and others have focused on the development of an artificial intestine, by placing intestinal stem cells on a bioscaffold that has an absorptive surface resembling native intestine, and taking advantage of neovascularization to develop a blood supply. This review will explore recent advances in biomaterials, vascularization, and progress towards development of a functional epithelium and mesenchymal niche, highlighting both success and ongoing challenges in the field. 2017-11-01 2018-01 /pmc/articles/PMC6002962/ /pubmed/28937976 http://dx.doi.org/10.1038/pr.2017.234 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Martin, Laura Y.
Ladd, Mitchell R.
Werts, Adam
Sodhi, Chhinder P.
March, John C.
Hackam, David J.
Tissue engineering for the treatment of short bowel syndrome in children
title Tissue engineering for the treatment of short bowel syndrome in children
title_full Tissue engineering for the treatment of short bowel syndrome in children
title_fullStr Tissue engineering for the treatment of short bowel syndrome in children
title_full_unstemmed Tissue engineering for the treatment of short bowel syndrome in children
title_short Tissue engineering for the treatment of short bowel syndrome in children
title_sort tissue engineering for the treatment of short bowel syndrome in children
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6002962/
https://www.ncbi.nlm.nih.gov/pubmed/28937976
http://dx.doi.org/10.1038/pr.2017.234
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