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Autologous cell-coated particles for the treatment of segmental bone defects—a new cell therapy approach

BACKGROUND: Adipose tissue-derived mesenchymal stem cells (AT-MSCs) are one of the most potent adult stem cells, capable of differentiating into bone, cartilage, adipose, muscle, and others. An innovative autologous AT-MSC-derived cell-based product (BonoFill-II) for bone tissue regeneration was dev...

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Autores principales: Ben-David, Dror, Fishman, Bettina, Rubin, Guy, Novak, Atara, Laevsky, Ilana, Kadouri, Avinoam, Nishri Katz, Yasmin, Burger, Ora, Zaretsky, Asaph, Bor, Noam, Tzur, Ephraim, Meretzki, Shai, Rozen, Nimrod
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6604185/
https://www.ncbi.nlm.nih.gov/pubmed/31262323
http://dx.doi.org/10.1186/s13018-019-1219-5
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author Ben-David, Dror
Fishman, Bettina
Rubin, Guy
Novak, Atara
Laevsky, Ilana
Kadouri, Avinoam
Nishri Katz, Yasmin
Burger, Ora
Zaretsky, Asaph
Bor, Noam
Tzur, Ephraim
Meretzki, Shai
Rozen, Nimrod
author_facet Ben-David, Dror
Fishman, Bettina
Rubin, Guy
Novak, Atara
Laevsky, Ilana
Kadouri, Avinoam
Nishri Katz, Yasmin
Burger, Ora
Zaretsky, Asaph
Bor, Noam
Tzur, Ephraim
Meretzki, Shai
Rozen, Nimrod
author_sort Ben-David, Dror
collection PubMed
description BACKGROUND: Adipose tissue-derived mesenchymal stem cells (AT-MSCs) are one of the most potent adult stem cells, capable of differentiating into bone, cartilage, adipose, muscle, and others. An innovative autologous AT-MSC-derived cell-based product (BonoFill-II) for bone tissue regeneration was developed to be suited as a bone graft for segmental bone defects. METHODS: BonoFill-II was transplanted into 8 sheep with 3.2-cm full cortex segmental defect formed in the tibia. Bone regeneration was followed by X-ray radiographs for 12 weeks. At experiment termination, the healed tibia bones were analyzed by computed tomography, histology, and mechanical tests. RESULTS: Our results indicate that one dose of BonoFill-II injectable formula led to an extensive bone growth within the transplantation site and to a complete closure of the critical gap in the sheep’s tibia in a relatively short time (8–12 weeks), with no inflammation and no other signs of graft rejection. This new and innovative product opens new prospects for the treatment of long bone defects. CONCLUSIONS: Injection of BonoFill-II (an innovative autologous cell therapy product for bone tissue regeneration) into a critical size segmental defect model (3.2 cm), generated in the sheep tibia, achieved full bridging of the gap in an extremely short period (8–12 weeks).
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spelling pubmed-66041852019-07-12 Autologous cell-coated particles for the treatment of segmental bone defects—a new cell therapy approach Ben-David, Dror Fishman, Bettina Rubin, Guy Novak, Atara Laevsky, Ilana Kadouri, Avinoam Nishri Katz, Yasmin Burger, Ora Zaretsky, Asaph Bor, Noam Tzur, Ephraim Meretzki, Shai Rozen, Nimrod J Orthop Surg Res Research Article BACKGROUND: Adipose tissue-derived mesenchymal stem cells (AT-MSCs) are one of the most potent adult stem cells, capable of differentiating into bone, cartilage, adipose, muscle, and others. An innovative autologous AT-MSC-derived cell-based product (BonoFill-II) for bone tissue regeneration was developed to be suited as a bone graft for segmental bone defects. METHODS: BonoFill-II was transplanted into 8 sheep with 3.2-cm full cortex segmental defect formed in the tibia. Bone regeneration was followed by X-ray radiographs for 12 weeks. At experiment termination, the healed tibia bones were analyzed by computed tomography, histology, and mechanical tests. RESULTS: Our results indicate that one dose of BonoFill-II injectable formula led to an extensive bone growth within the transplantation site and to a complete closure of the critical gap in the sheep’s tibia in a relatively short time (8–12 weeks), with no inflammation and no other signs of graft rejection. This new and innovative product opens new prospects for the treatment of long bone defects. CONCLUSIONS: Injection of BonoFill-II (an innovative autologous cell therapy product for bone tissue regeneration) into a critical size segmental defect model (3.2 cm), generated in the sheep tibia, achieved full bridging of the gap in an extremely short period (8–12 weeks). BioMed Central 2019-07-01 /pmc/articles/PMC6604185/ /pubmed/31262323 http://dx.doi.org/10.1186/s13018-019-1219-5 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Ben-David, Dror
Fishman, Bettina
Rubin, Guy
Novak, Atara
Laevsky, Ilana
Kadouri, Avinoam
Nishri Katz, Yasmin
Burger, Ora
Zaretsky, Asaph
Bor, Noam
Tzur, Ephraim
Meretzki, Shai
Rozen, Nimrod
Autologous cell-coated particles for the treatment of segmental bone defects—a new cell therapy approach
title Autologous cell-coated particles for the treatment of segmental bone defects—a new cell therapy approach
title_full Autologous cell-coated particles for the treatment of segmental bone defects—a new cell therapy approach
title_fullStr Autologous cell-coated particles for the treatment of segmental bone defects—a new cell therapy approach
title_full_unstemmed Autologous cell-coated particles for the treatment of segmental bone defects—a new cell therapy approach
title_short Autologous cell-coated particles for the treatment of segmental bone defects—a new cell therapy approach
title_sort autologous cell-coated particles for the treatment of segmental bone defects—a new cell therapy approach
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6604185/
https://www.ncbi.nlm.nih.gov/pubmed/31262323
http://dx.doi.org/10.1186/s13018-019-1219-5
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