Volume 13, Issue 11 pp. 1943-1954
RESEARCH ARTICLE

In vivo implantation of a tissue engineered stem cell seeded hemi-laryngeal replacement maintains airway, phonation, and swallowing in pigs

P. Herrmann

P. Herrmann

NPIMR, Harrow, UK

UCL Ear Institute, Royal National Throat Nose and Ear Hospital, London, UK

[Corrections added on 11October2019 after first online publication: In Section 2.4.1 paragraph, line 3, the seeding density should read “1.5 × 10 ” and not “1.5 × 10”. Likewise, in the supporting information Figure S2, 5th column of the Table should be amended to read “Seeded MSC (x105/cm2)” and not “Seeded MSC (x106/cm2)”. This has been corrected in this version.]These two authors contributed equally.Search for more papers by this author
T. Ansari

Corresponding Author

T. Ansari

NPIMR, Harrow, UK

These two authors contributed equally.

Correspondence

Tahera Ansari or Martin Birchall, NPIMR, Block Y level 3 Watford Rd. Harrow, HA1 3UJ, UK.

Email: [email protected]; [email protected]

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A. Southgate

A. Southgate

NPIMR, Harrow, UK

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A. Varanou Jenkins

A. Varanou Jenkins

Department Lungs for Living Research Centre, Division of Medicine, Rayne Building, University College London, London, UK

MRC Cancer Unit, Hutchison/MRC Research Centre, University of Cambridge, CB2 0XZ, UK.Search for more papers by this author
L. Partington

L. Partington

Department of Haematology, University College London, London, UK

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C. Carvalho

C. Carvalho

Department of Haematology, University College London, London, UK

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S. Janes

S. Janes

Department Lungs for Living Research Centre, Division of Medicine, Rayne Building, University College London, London, UK

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M. Lowdell

M. Lowdell

Department of Haematology, University College London, London, UK

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P.D. Sibbons

P.D. Sibbons

NPIMR, Harrow, UK

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M.A. Birchall

Corresponding Author

M.A. Birchall

UCL Ear Institute, Royal National Throat Nose and Ear Hospital, London, UK

Correspondence

Tahera Ansari or Martin Birchall, NPIMR, Block Y level 3 Watford Rd. Harrow, HA1 3UJ, UK.

Email: [email protected]; [email protected]

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First published: 19 October 2017
Citations: 18

Funding information

Medical Research Council, Grant/Award Number: G1001539, RegenVOX1 (G1001539); NPIMR

[Corrections added on 11 October 2019 after first online publication: The article was first published online on 17th December 2017 in the Journal of Tissue Engineering and Regenerative Medicine. The authors and University College London (UCL) subsequently identified errors within Figures 1 and 2 which they would like to correct. A screening committee, convened at the authors' host institution, UCL, working with the authors and others, confirmed in their report dated December 2018 that Figures 1 and 2 had been duplicated from an article previously published by the same authors in STEM CELLS Translational Medicine (Ansari et al., 2017, Stem Cell-Based Tissue-Engineered Laryngeal Replacement. STEM CELLS Translational Medicine, 6: 677–687. DOI: 10.5966/sctm.2016–0130). The report expressed satisfaction with the authors' explanation for the errors, and found that the duplicated images did not affect the results or conclusions published in the paper. UCL recommended that the authors submit a correction for the figures in question. Thus, the authors have made changes to Figures 1 and 2 as described in the respective figure legends. The authors would like to apologise for these errors].
[Corrections added on 11October2019 after first online publication: In Section 2.4.1 paragraph, line 3, the seeding density should read “1.5 × 10 ” and not “1.5 × 10”. Likewise, in the supporting information Figure S2, 5th column of the Table should be amended to read “Seeded MSC (x105/cm2)” and not “Seeded MSC (x106/cm2)”. This has been corrected in this version.]

Abstract

Laryngeal functional impairment relating to swallowing, vocalisation, and respiration can be life changing and devastating for patients. A tissue engineering approach to regenerating vocal folds would represent a significant advantage over current clinical practice.

Porcine hemi-larynx were de-cellularised under negative pressure. The resultant acellular scaffold was seeded with human bone marrow derived mesenchymal stem cells and primary human epithelial cells. Seeded scaffolds were implanted orthotopically into a defect created in the thyroid cartilage in 8 pigs and monitored in vivo for 2 months. In vivo assessments consisted of mucosal brushing and bronchoscopy at 1, 2, 4, and 8 weeks post implantation followed by histological evaluation post termination. The implanted graft had no adverse effect on respiratory function in 6 of the 8 pigs; none of the pigs had problems with swallowing or vocalisation. Six out of the 8 animals survived to the planned termination date; 2 animals were terminated due to mild stenosis and deep tissue abscess formation, respectively. Human epithelial cells from mucosal brushings could only be identified at Weeks 1 and 4. The explanted tissue showed complete epithelialisation of the mucosal surface and the development of rudimentary vocal folds. However, there was no evidence of cartilage remodelling at the relatively early censor point. Single stage partial laryngeal replacement is a safe surgical procedure. Replacement with a tissue engineered laryngeal graft as a single procedure is surgically feasible and results in appropriate mucosal coverage and rudimentary vocal fold development.

CONFLICT OF INTEREST

The authors have declared that there is no conflict of interest.

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