Clinical transplantation of a tissue-engineered airway
- PMID: 19022496
- DOI: 10.1016/S0140-6736(08)61598-6
Clinical transplantation of a tissue-engineered airway
Erratum in
- Lancet. 2009 Feb 7;373(9662):462
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Department of Error.Lancet. 2019 Jul 20;394(10194):218. doi: 10.1016/S0140-6736(19)31562-4. Lancet. 2019. PMID: 31327368 No abstract available.
Retraction in
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Retraction: Clinical transplantation of a tissue-engineered airway.Lancet. 2023 Oct 28;402(10412):1510. doi: 10.1016/S0140-6736(23)02341-3. Lancet. 2023. PMID: 37898523 No abstract available.
Expression of concern in
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Expression of concern: Clinical transplantation of a tissue-engineered airway.Lancet. 2023 Feb 18;401(10376):536. doi: 10.1016/S0140-6736(23)00293-3. Epub 2023 Feb 8. Lancet. 2023. PMID: 36773618 No abstract available.
Abstract
Background: The loss of a normal airway is devastating. Attempts to replace large airways have met with serious problems. Prerequisites for a tissue-engineered replacement are a suitable matrix, cells, ideal mechanical properties, and the absence of antigenicity. We aimed to bioengineer tubular tracheal matrices, using a tissue-engineering protocol, and to assess the application of this technology in a patient with end-stage airway disease.
Methods: We removed cells and MHC antigens from a human donor trachea, which was then readily colonised by epithelial cells and mesenchymal stem-cell-derived chondrocytes that had been cultured from cells taken from the recipient (a 30-year old woman with end-stage bronchomalacia). This graft was then used to replace the recipient's left main bronchus.
Findings: The graft immediately provided the recipient with a functional airway, improved her quality of life, and had a normal appearance and mechanical properties at 4 months. The patient had no anti-donor antibodies and was not on immunosuppressive drugs.
Interpretation: The results show that we can produce a cellular, tissue-engineered airway with mechanical properties that allow normal functioning, and which is free from the risks of rejection. The findings suggest that autologous cells combined with appropriate biomaterials might provide successful treatment for patients with serious clinical disorders.
Comment in
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Tissue-engineered airway replacement.Lancet. 2008 Dec 13;372(9655):2003-4. doi: 10.1016/S0140-6736(08)61599-8. Epub 2008 Nov 18. Lancet. 2008. PMID: 19022497 No abstract available.
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Clinical transplantation of a tissue-engineered airway.Lancet. 2009 Feb 28;373(9665):717; author reply 718-9. doi: 10.1016/S0140-6736(09)60428-1. Lancet. 2009. PMID: 19249621 No abstract available.
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Clinical transplantation of a tissue-engineered airway.Lancet. 2009 Feb 28;373(9665):717-8; author reply 718-9. doi: 10.1016/S0140-6736(09)60429-3. Lancet. 2009. PMID: 19249622 No abstract available.
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Clinical transplantation of a tissue-engineered airway.Lancet. 2009 Feb 28;373(9665):718; author reply 718-9. doi: 10.1016/S0140-6736(09)60430-X. Lancet. 2009. PMID: 19249624 No abstract available.
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Patient follow-up after tissue-engineered airway transplantation.Lancet. 2019 Mar 16;393(10176):1099. doi: 10.1016/S0140-6736(19)30485-4. Epub 2019 Mar 1. Lancet. 2019. PMID: 30833040 No abstract available.
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Time to retract Lancet paper on tissue engineered trachea transplants.BMJ. 2022 Mar 2;376:o498. doi: 10.1136/bmj.o498. BMJ. 2022. PMID: 35236744 No abstract available.
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