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Equine Allogeneic Chondrogenic Induced Mesenchymal Stem Cells Are an Effective Treatment for Degenerative Joint Disease in Horses

Degenerative joint disease is one of the main causes of equine early retirement from pleasure riding or a performance career. The disease is initially triggered by an abnormal loading of normal cartilage or a normal loading of abnormal cartilage. This primary insult is accompanied with joint inflamm...

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Autores principales: Broeckx, Sarah Y., Seys, Bert, Suls, Marc, Vandenberghe, Aurélie, Mariën, Tom, Adriaensen, Edouard, Declercq, Jeroen, Van Hecke, Lore, Braun, Gabriele, Hellmann, Klaus, Spaas, Jan H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc., publishers 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6441287/
https://www.ncbi.nlm.nih.gov/pubmed/30623737
http://dx.doi.org/10.1089/scd.2018.0061
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author Broeckx, Sarah Y.
Seys, Bert
Suls, Marc
Vandenberghe, Aurélie
Mariën, Tom
Adriaensen, Edouard
Declercq, Jeroen
Van Hecke, Lore
Braun, Gabriele
Hellmann, Klaus
Spaas, Jan H.
author_facet Broeckx, Sarah Y.
Seys, Bert
Suls, Marc
Vandenberghe, Aurélie
Mariën, Tom
Adriaensen, Edouard
Declercq, Jeroen
Van Hecke, Lore
Braun, Gabriele
Hellmann, Klaus
Spaas, Jan H.
author_sort Broeckx, Sarah Y.
collection PubMed
description Degenerative joint disease is one of the main causes of equine early retirement from pleasure riding or a performance career. The disease is initially triggered by an abnormal loading of normal cartilage or a normal loading of abnormal cartilage. This primary insult is accompanied with joint inflammation, which leads to further progressive degeneration of the articular cartilage and changes in the surrounding tissues. Therefore, in search for an effective treatment, 75 adult horses with early signs of degenerative fetlock joint disease were enrolled in a randomized, multicenter, double-blinded, and placebo-controlled study. Fifty animals were injected intra-articularly with the investigational veterinary product (IVP) consisting of allogeneic chondrogenic induced mesenchymal stem cells (ciMSCs) with equine allogeneic plasma, and 25 horses were injected with 0.9% NaCl (saline) control product. From week 3 to 18 after treatment, lameness scores (P < 0.001), flexion test responses (P < 0.034), and joint effusion scores (P < 0.001) were remarkably superior in IVP-treated horses. Besides nasal discharge in both treatment groups, no adverse events were observed during the entire study period. On long-term follow-up (1 year), significantly more investigational product-treated horses were working at training level or were returned to their previous level of work (P < 0.001).
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spelling pubmed-64412872019-04-01 Equine Allogeneic Chondrogenic Induced Mesenchymal Stem Cells Are an Effective Treatment for Degenerative Joint Disease in Horses Broeckx, Sarah Y. Seys, Bert Suls, Marc Vandenberghe, Aurélie Mariën, Tom Adriaensen, Edouard Declercq, Jeroen Van Hecke, Lore Braun, Gabriele Hellmann, Klaus Spaas, Jan H. Stem Cells Dev Clinical Trial Degenerative joint disease is one of the main causes of equine early retirement from pleasure riding or a performance career. The disease is initially triggered by an abnormal loading of normal cartilage or a normal loading of abnormal cartilage. This primary insult is accompanied with joint inflammation, which leads to further progressive degeneration of the articular cartilage and changes in the surrounding tissues. Therefore, in search for an effective treatment, 75 adult horses with early signs of degenerative fetlock joint disease were enrolled in a randomized, multicenter, double-blinded, and placebo-controlled study. Fifty animals were injected intra-articularly with the investigational veterinary product (IVP) consisting of allogeneic chondrogenic induced mesenchymal stem cells (ciMSCs) with equine allogeneic plasma, and 25 horses were injected with 0.9% NaCl (saline) control product. From week 3 to 18 after treatment, lameness scores (P < 0.001), flexion test responses (P < 0.034), and joint effusion scores (P < 0.001) were remarkably superior in IVP-treated horses. Besides nasal discharge in both treatment groups, no adverse events were observed during the entire study period. On long-term follow-up (1 year), significantly more investigational product-treated horses were working at training level or were returned to their previous level of work (P < 0.001). Mary Ann Liebert, Inc., publishers 2019-03-15 2019-03-08 /pmc/articles/PMC6441287/ /pubmed/30623737 http://dx.doi.org/10.1089/scd.2018.0061 Text en © Sarah Y. Broeckx et al. 2019; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Trial
Broeckx, Sarah Y.
Seys, Bert
Suls, Marc
Vandenberghe, Aurélie
Mariën, Tom
Adriaensen, Edouard
Declercq, Jeroen
Van Hecke, Lore
Braun, Gabriele
Hellmann, Klaus
Spaas, Jan H.
Equine Allogeneic Chondrogenic Induced Mesenchymal Stem Cells Are an Effective Treatment for Degenerative Joint Disease in Horses
title Equine Allogeneic Chondrogenic Induced Mesenchymal Stem Cells Are an Effective Treatment for Degenerative Joint Disease in Horses
title_full Equine Allogeneic Chondrogenic Induced Mesenchymal Stem Cells Are an Effective Treatment for Degenerative Joint Disease in Horses
title_fullStr Equine Allogeneic Chondrogenic Induced Mesenchymal Stem Cells Are an Effective Treatment for Degenerative Joint Disease in Horses
title_full_unstemmed Equine Allogeneic Chondrogenic Induced Mesenchymal Stem Cells Are an Effective Treatment for Degenerative Joint Disease in Horses
title_short Equine Allogeneic Chondrogenic Induced Mesenchymal Stem Cells Are an Effective Treatment for Degenerative Joint Disease in Horses
title_sort equine allogeneic chondrogenic induced mesenchymal stem cells are an effective treatment for degenerative joint disease in horses
topic Clinical Trial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6441287/
https://www.ncbi.nlm.nih.gov/pubmed/30623737
http://dx.doi.org/10.1089/scd.2018.0061
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