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Background: It has been difficult to perform tracheal allotransplantation without immunosuppression. To determine whether decellularized trachea can be used in tracheal replacement, we evaluated the viability of decellularized tracheal allografts in a rabbit model of immunosuppressant-free transplantation.
Method: Half allograft (Group 1, n = 7) was harvested from adult New Zealand white rabbits, subjected to a detergent-enzymatic method (containing sodium deoxycholate/DNase lavations) of decellularization for as many cycles as needed, and the other half was stored in phosphate-buffered saline at 4°C as a control (Group 2, n = 7). Bioengineered and control tracheas were then implanted in 14 age-matched rabbits.
Results: In Group 1 (decellularized), all rabbits survived, whereas in Group 2(control), all rabbits died of airway obstruction between 20 days and 45 days after operation. Histologically, the decellularized allografts displayed complete regeneration of epithelium and cartilage, but the fresh allografts showed inflammatory changes, no epithelium, and no cartilage.
Conclusions: Complete regeneration of epithelium and cartilage tracheal rings occurred after the implantation of decellularized tracheal allografts without immunosuppression. We demonstrate that the decellularized process reduces the allogeneic response to the trachea. Therefore, we believe that the decellularized tracheal allograft is an excellent choice for tracheal replacement. To our knowledge, this is the first study to observe the long-term (1 year) prognosis of this transplanted trachea.
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http://dx.doi.org/10.1016/j.asjsur.2017.02.007 | DOI Listing |
Bioengineering (Basel)
June 2025
Department of Animal Anatomy, University of Marilia (UNIMAR), Marília 17525-902, Brazil.
Tracheal defects have been the focus of research since the 19th century, but reconstructing this complex structure remains challenging. Identifying a safe, effective tracheal substitute is a key goal of surgery. This integrative review explores current tracheal substitutes and tissue engineering techniques.
View Article and Find Full Text PDFMater Today Bio
August 2025
Clinical Medical College, Yangzhou University, Yangzhou, 225009, China.
The success of tracheal transplantation depends on the rapid establishment of vascularization and epithelialization to support functional tissue formation. This study presents an innovative approach for in situ transplantation of a biomimetic tracheal graft, integrating microvascularization and epithelialization. First, endothelial progenitor cells (EPCs) and mesenchymal stem cells (MSCs) were isolated and purified from bone marrow, serving as seed cells for graft vascularization and epithelialization.
View Article and Find Full Text PDFAdv Healthc Mater
June 2025
Department of Biomedical Engineering, College of Medicine and College of Engineering, National Taiwan University, No.1, Sec. 1, Jen Ai Rd., Taipei, 100233, Taiwan (R.O.C.).
Native tracheal cartilage exhibits limited regenerative capacity, making the search for suitable biomaterials for tracheal repair a persistent challenge. In this study, a non-decellularized cryopreserved aortic allograft (CAo) is investigated as a scaffold for tracheal cartilage regeneration. Originally used to reconstruct infected aortas, CAo retains key features of a large artery-abundant elastic fibers and smooth muscle cells-and demonstrates favorable in vitro biocompatibility with chondrocytes.
View Article and Find Full Text PDFLaryngoscope
September 2025
The Ohio State University College of Medicine, Columbus, Ohio, USA.
Objectives: Tracheal allografts have been used to reconstruct the human airway. However, the need for immunosuppression could ultimately limit their clinical translation. Partial decellularization (PD) has the potential to eliminate allograft immunogenicity while preserving donor cartilage.
View Article and Find Full Text PDFJ Nanobiotechnology
April 2025
Northern Jiangsu People's Hospital Affiliated to Yangzhou University, Yangzhou University, Yangzhou, 225001, China.
Tracheal reconstruction presents a significant global clinical challenge due to the unique structure and function of the trachea, which complicates its repair. Key challenges include restoring tracheal function post-transplantation, managing surgical complications, and ensuring the long-term survival of transplanted tissue. Furthermore, adequate vascularization of the transplanted trachea, along with the repair of cartilage and epithelial cells, is critical for facilitating functional recovery and successful reconstruction.
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