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Effect of Allogeneic Oral Mucosa Mesenchymal Stromal Cells on Equine Wound Repair
OBJECTIVE: To assess the clinical value and safety of the application of allogeneic equine oral mucosa mesenchymal stromal cells (OM-MSCs) to wounds. Animals. 8 healthy adult horses without front limb skin lesions or musculoskeletal disease. Procedures. Stem cells were isolated from the oral mucosa...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8692048/ https://www.ncbi.nlm.nih.gov/pubmed/34950446 http://dx.doi.org/10.1155/2021/5024905 |
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author | Di Francesco, Paola Cajon, Pauline Desterke, Christophe Perron Lepage, Marie-France Lataillade, Jean-Jacques Kadri, Tewfik Lepage, Olivier M. |
author_facet | Di Francesco, Paola Cajon, Pauline Desterke, Christophe Perron Lepage, Marie-France Lataillade, Jean-Jacques Kadri, Tewfik Lepage, Olivier M. |
author_sort | Di Francesco, Paola |
collection | PubMed |
description | OBJECTIVE: To assess the clinical value and safety of the application of allogeneic equine oral mucosa mesenchymal stromal cells (OM-MSCs) to wounds. Animals. 8 healthy adult horses without front limb skin lesions or musculoskeletal disease. Procedures. Stem cells were isolated from the oral mucosa of a donor horse. Horses were subjected to the creation of eight full-thickness cutaneous wounds, two on each distal forelimb (FL) and two on both sides of the thorax (TH). Each wound was subjected to one out of four treatments: no medication (T1), hyaluronic acid- (HA-) gel containing OM-MSC (T2), HA-gel containing OM-MSC secretome (T3), and HA-gel alone (T4). Gross macroscopic evaluation and laser digital photographic documentation were regularly performed to allow wound assessment including wound surface area. Full-thickness skin punch biopsy was performed at each site before wound induction (D0, normal skin) and after complete wound healing (D62, repaired skin). RESULTS: All wounds healed without adverse effect at D62. Distal limb wounds are slower to heal than body wounds. OM-MSC and its secretome have a positive impact on TH wound contraction. OM-MSC has a positive impact on the contraction and epithelialization of FL wounds. No significant difference between wound sites before and after treatment was noted at histological examination. Conclusion and Clinical Relevance. Using horse cells harvested from oral mucosa is a feasible technique to produce OM-MSC or its secretome. The gel produced by the combination of these biologic components with HA shows a positive impact when applied during the early stage of wound healing. |
format | Online Article Text |
id | pubmed-8692048 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-86920482021-12-22 Effect of Allogeneic Oral Mucosa Mesenchymal Stromal Cells on Equine Wound Repair Di Francesco, Paola Cajon, Pauline Desterke, Christophe Perron Lepage, Marie-France Lataillade, Jean-Jacques Kadri, Tewfik Lepage, Olivier M. Vet Med Int Research Article OBJECTIVE: To assess the clinical value and safety of the application of allogeneic equine oral mucosa mesenchymal stromal cells (OM-MSCs) to wounds. Animals. 8 healthy adult horses without front limb skin lesions or musculoskeletal disease. Procedures. Stem cells were isolated from the oral mucosa of a donor horse. Horses were subjected to the creation of eight full-thickness cutaneous wounds, two on each distal forelimb (FL) and two on both sides of the thorax (TH). Each wound was subjected to one out of four treatments: no medication (T1), hyaluronic acid- (HA-) gel containing OM-MSC (T2), HA-gel containing OM-MSC secretome (T3), and HA-gel alone (T4). Gross macroscopic evaluation and laser digital photographic documentation were regularly performed to allow wound assessment including wound surface area. Full-thickness skin punch biopsy was performed at each site before wound induction (D0, normal skin) and after complete wound healing (D62, repaired skin). RESULTS: All wounds healed without adverse effect at D62. Distal limb wounds are slower to heal than body wounds. OM-MSC and its secretome have a positive impact on TH wound contraction. OM-MSC has a positive impact on the contraction and epithelialization of FL wounds. No significant difference between wound sites before and after treatment was noted at histological examination. Conclusion and Clinical Relevance. Using horse cells harvested from oral mucosa is a feasible technique to produce OM-MSC or its secretome. The gel produced by the combination of these biologic components with HA shows a positive impact when applied during the early stage of wound healing. Hindawi 2021-12-14 /pmc/articles/PMC8692048/ /pubmed/34950446 http://dx.doi.org/10.1155/2021/5024905 Text en Copyright © 2021 Paola Di Francesco et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Di Francesco, Paola Cajon, Pauline Desterke, Christophe Perron Lepage, Marie-France Lataillade, Jean-Jacques Kadri, Tewfik Lepage, Olivier M. Effect of Allogeneic Oral Mucosa Mesenchymal Stromal Cells on Equine Wound Repair |
title | Effect of Allogeneic Oral Mucosa Mesenchymal Stromal Cells on Equine Wound Repair |
title_full | Effect of Allogeneic Oral Mucosa Mesenchymal Stromal Cells on Equine Wound Repair |
title_fullStr | Effect of Allogeneic Oral Mucosa Mesenchymal Stromal Cells on Equine Wound Repair |
title_full_unstemmed | Effect of Allogeneic Oral Mucosa Mesenchymal Stromal Cells on Equine Wound Repair |
title_short | Effect of Allogeneic Oral Mucosa Mesenchymal Stromal Cells on Equine Wound Repair |
title_sort | effect of allogeneic oral mucosa mesenchymal stromal cells on equine wound repair |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8692048/ https://www.ncbi.nlm.nih.gov/pubmed/34950446 http://dx.doi.org/10.1155/2021/5024905 |
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