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Novel Therapy for Acquired Tracheomalacia with a Tissue-Engineered Extraluminal Tracheal Splint and Autologous Mesenchymal-Derived Chondrocytes

Introduction  Acquired tracheomalacia (ATM) is characterized by a loss of structural strength of the tracheal framework, resulting in airway collapse during breathing. Near half of the patients undergoing prolonged invasive mechanical ventilation will suffer tracheal lesions. Treatment for ATM inclu...

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Autores principales: Melgarejo-Ramírez, Yaaziel, Ceballos-Cantú, Juan C., Montes-Olave, Eric de J., Hernández-Tapia, Bruno, Rojas-Figueroa, Víctor, Ramírez-Arroyo, Gabriela, Cortés-Acosta, Fabiana, Dorantes-Pavón, Mario, Lecona-Butrón, Hugo, Beltrán-Rodríguez-Cabo, Olga E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Thieme Revinter Publicações Ltda. 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10147475/
https://www.ncbi.nlm.nih.gov/pubmed/37125371
http://dx.doi.org/10.1055/s-0042-1746194
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author Melgarejo-Ramírez, Yaaziel
Ceballos-Cantú, Juan C.
Montes-Olave, Eric de J.
Hernández-Tapia, Bruno
Rojas-Figueroa, Víctor
Ramírez-Arroyo, Gabriela
Cortés-Acosta, Fabiana
Dorantes-Pavón, Mario
Lecona-Butrón, Hugo
Beltrán-Rodríguez-Cabo, Olga E.
author_facet Melgarejo-Ramírez, Yaaziel
Ceballos-Cantú, Juan C.
Montes-Olave, Eric de J.
Hernández-Tapia, Bruno
Rojas-Figueroa, Víctor
Ramírez-Arroyo, Gabriela
Cortés-Acosta, Fabiana
Dorantes-Pavón, Mario
Lecona-Butrón, Hugo
Beltrán-Rodríguez-Cabo, Olga E.
author_sort Melgarejo-Ramírez, Yaaziel
collection PubMed
description Introduction  Acquired tracheomalacia (ATM) is characterized by a loss of structural strength of the tracheal framework, resulting in airway collapse during breathing. Near half of the patients undergoing prolonged invasive mechanical ventilation will suffer tracheal lesions. Treatment for ATM includes external splinting with rib grafts, prosthetic materials, and tracheal resection. Failure in the use of prosthetic materials has made reconsidering natural origin scaffolds and tissue engineering as a suitable alternative. Objective  To restore adequate airway patency in an ovine model with surgically-induced ATM employing a tissue-engineered extraluminal tracheal splint (TE-ETS). Methods  In the present prospective pilot study, tracheal rings were partially resected to induce airway collapse in 16 Suffolk sheep ( Ovis aries ). The TE-ETS was developed with autologous mesenchymal-derived chondrocytes and allogenic decellularized tracheal segments and was implanted above debilitated tracheal rings. The animals were followed-up at 8, 12, and 16 weeks and at 1-year postinsertion. Flexible tracheoscopies were performed at each stage. After sacrifice, a histopathological study of the trachea and the splint were performed. Results  The TE-ETS prevented airway collapse for 16 weeks and up to 1-year postinsertion. Tracheoscopies revealed a noncollapsing airway during inspiration. Histopathological analyses showed the organization of mesenchymal-derived chondrocytes in lacunae, the proliferation of blood vessels, and recovery of epithelial tissue subjacent to the splint. Splints without autologous cells did not prevent airway collapse. Conclusion  It is possible to treat acquired tracheomalacia with TE-ETS without further surgical removal since it undergoes physiological degradation. The present study supports the development of tissue-engineered tracheal substitutes for airway disease.
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spelling pubmed-101474752023-04-29 Novel Therapy for Acquired Tracheomalacia with a Tissue-Engineered Extraluminal Tracheal Splint and Autologous Mesenchymal-Derived Chondrocytes Melgarejo-Ramírez, Yaaziel Ceballos-Cantú, Juan C. Montes-Olave, Eric de J. Hernández-Tapia, Bruno Rojas-Figueroa, Víctor Ramírez-Arroyo, Gabriela Cortés-Acosta, Fabiana Dorantes-Pavón, Mario Lecona-Butrón, Hugo Beltrán-Rodríguez-Cabo, Olga E. Int Arch Otorhinolaryngol Introduction  Acquired tracheomalacia (ATM) is characterized by a loss of structural strength of the tracheal framework, resulting in airway collapse during breathing. Near half of the patients undergoing prolonged invasive mechanical ventilation will suffer tracheal lesions. Treatment for ATM includes external splinting with rib grafts, prosthetic materials, and tracheal resection. Failure in the use of prosthetic materials has made reconsidering natural origin scaffolds and tissue engineering as a suitable alternative. Objective  To restore adequate airway patency in an ovine model with surgically-induced ATM employing a tissue-engineered extraluminal tracheal splint (TE-ETS). Methods  In the present prospective pilot study, tracheal rings were partially resected to induce airway collapse in 16 Suffolk sheep ( Ovis aries ). The TE-ETS was developed with autologous mesenchymal-derived chondrocytes and allogenic decellularized tracheal segments and was implanted above debilitated tracheal rings. The animals were followed-up at 8, 12, and 16 weeks and at 1-year postinsertion. Flexible tracheoscopies were performed at each stage. After sacrifice, a histopathological study of the trachea and the splint were performed. Results  The TE-ETS prevented airway collapse for 16 weeks and up to 1-year postinsertion. Tracheoscopies revealed a noncollapsing airway during inspiration. Histopathological analyses showed the organization of mesenchymal-derived chondrocytes in lacunae, the proliferation of blood vessels, and recovery of epithelial tissue subjacent to the splint. Splints without autologous cells did not prevent airway collapse. Conclusion  It is possible to treat acquired tracheomalacia with TE-ETS without further surgical removal since it undergoes physiological degradation. The present study supports the development of tissue-engineered tracheal substitutes for airway disease. Thieme Revinter Publicações Ltda. 2022-09-27 /pmc/articles/PMC10147475/ /pubmed/37125371 http://dx.doi.org/10.1055/s-0042-1746194 Text en Fundação Otorrinolaringologia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commecial purposes, or adapted, remixed, transformed or built upon. ( https://creativecommons.org/licenses/by-nc-nd/4.0/ ) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License, which permits unrestricted reproduction and distribution, for non-commercial purposes only; and use and reproduction, but not distribution, of adapted material for non-commercial purposes only, provided the original work is properly cited.
spellingShingle Melgarejo-Ramírez, Yaaziel
Ceballos-Cantú, Juan C.
Montes-Olave, Eric de J.
Hernández-Tapia, Bruno
Rojas-Figueroa, Víctor
Ramírez-Arroyo, Gabriela
Cortés-Acosta, Fabiana
Dorantes-Pavón, Mario
Lecona-Butrón, Hugo
Beltrán-Rodríguez-Cabo, Olga E.
Novel Therapy for Acquired Tracheomalacia with a Tissue-Engineered Extraluminal Tracheal Splint and Autologous Mesenchymal-Derived Chondrocytes
title Novel Therapy for Acquired Tracheomalacia with a Tissue-Engineered Extraluminal Tracheal Splint and Autologous Mesenchymal-Derived Chondrocytes
title_full Novel Therapy for Acquired Tracheomalacia with a Tissue-Engineered Extraluminal Tracheal Splint and Autologous Mesenchymal-Derived Chondrocytes
title_fullStr Novel Therapy for Acquired Tracheomalacia with a Tissue-Engineered Extraluminal Tracheal Splint and Autologous Mesenchymal-Derived Chondrocytes
title_full_unstemmed Novel Therapy for Acquired Tracheomalacia with a Tissue-Engineered Extraluminal Tracheal Splint and Autologous Mesenchymal-Derived Chondrocytes
title_short Novel Therapy for Acquired Tracheomalacia with a Tissue-Engineered Extraluminal Tracheal Splint and Autologous Mesenchymal-Derived Chondrocytes
title_sort novel therapy for acquired tracheomalacia with a tissue-engineered extraluminal tracheal splint and autologous mesenchymal-derived chondrocytes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10147475/
https://www.ncbi.nlm.nih.gov/pubmed/37125371
http://dx.doi.org/10.1055/s-0042-1746194
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