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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Thieme Revinter Publicações Ltda.
2022
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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. |
format | Online Article Text |
id | pubmed-10147475 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Thieme Revinter Publicações Ltda. |
record_format | MEDLINE/PubMed |
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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