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Amniotic suspension allograft improves pain and function in a rat meniscal tear-induced osteoarthritis model

BACKGROUND: Osteoarthritis is a degenerative disease of the knee that affects 250 million people worldwide. Due to the rising incidence of knee replacement and revision surgery, there is a need for a nonsurgical treatment to reduce pain and improve function in patients with knee osteoarthritis. Plac...

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Autores principales: Kimmerling, Kelly A., Gomoll, Andreas H., Farr, Jack, Mowry, Katie C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8895852/
https://www.ncbi.nlm.nih.gov/pubmed/35246217
http://dx.doi.org/10.1186/s13075-022-02750-9
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author Kimmerling, Kelly A.
Gomoll, Andreas H.
Farr, Jack
Mowry, Katie C.
author_facet Kimmerling, Kelly A.
Gomoll, Andreas H.
Farr, Jack
Mowry, Katie C.
author_sort Kimmerling, Kelly A.
collection PubMed
description BACKGROUND: Osteoarthritis is a degenerative disease of the knee that affects 250 million people worldwide. Due to the rising incidence of knee replacement and revision surgery, there is a need for a nonsurgical treatment to reduce pain and improve function in patients with knee osteoarthritis. Placental-derived allografts, such as an amniotic suspension allograft (ASA), provide growth factors and cytokines that could potentially modulate the inflammatory environment of osteoarthritis. The purpose of this study was to evaluate the efficacy of ASA in a rat medial meniscal tear (MMT) induced osteoarthritis model through histology, microCT, synovial fluid biomarkers, and behavioral testing. METHODS: Rats underwent MMT surgery at day − 7; at day 0, rats were injected with either ASA, vehicle control, or fibroblast growth factor-18 (FGF18). Behavioral testing, including gait analysis, pain threshold, incapacitance, and knee swelling were evaluated in-life, along with histology, microCT analysis of cartilage, and synovial fluid testing post-sacrifice. One MMT cohort was sacrificed at day 10, the other at day 21. A third cohort acted as a safety arm and did not receive MMT surgery; these rats were injected with either vehicle control or ASA and evaluated at day 3 and day 21. RESULTS: Behavioral testing showed a significant improvement in pain threshold, incapacitance, and gait following an injection of ASA. MicroCT showed significant improvements in cartilage thickness and attenuation at day 10 only, and histology showed no detrimental effects compared to the vehicle control at day 21. Synovial fluid analysis showed a significant increase in anti-inflammatory IL-10. The safety cohort showed no significant differences except for an increase in synovitis at day 21, which could be evidence of a xenogeneic response in this model. CONCLUSIONS: In this study, an injection of ASA was well tolerated with no adverse events. Improvements in pain and function, along with cartilage properties at day 10, were observed. Increases in anti-inflammatory cytokines was also seen, along with no significant cartilage degeneration at day 21 compared to the vehicle control. This study provides evidence for the use of ASA as a nonsurgical treatment for knee OA. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13075-022-02750-9.
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spelling pubmed-88958522022-03-10 Amniotic suspension allograft improves pain and function in a rat meniscal tear-induced osteoarthritis model Kimmerling, Kelly A. Gomoll, Andreas H. Farr, Jack Mowry, Katie C. Arthritis Res Ther Research Article BACKGROUND: Osteoarthritis is a degenerative disease of the knee that affects 250 million people worldwide. Due to the rising incidence of knee replacement and revision surgery, there is a need for a nonsurgical treatment to reduce pain and improve function in patients with knee osteoarthritis. Placental-derived allografts, such as an amniotic suspension allograft (ASA), provide growth factors and cytokines that could potentially modulate the inflammatory environment of osteoarthritis. The purpose of this study was to evaluate the efficacy of ASA in a rat medial meniscal tear (MMT) induced osteoarthritis model through histology, microCT, synovial fluid biomarkers, and behavioral testing. METHODS: Rats underwent MMT surgery at day − 7; at day 0, rats were injected with either ASA, vehicle control, or fibroblast growth factor-18 (FGF18). Behavioral testing, including gait analysis, pain threshold, incapacitance, and knee swelling were evaluated in-life, along with histology, microCT analysis of cartilage, and synovial fluid testing post-sacrifice. One MMT cohort was sacrificed at day 10, the other at day 21. A third cohort acted as a safety arm and did not receive MMT surgery; these rats were injected with either vehicle control or ASA and evaluated at day 3 and day 21. RESULTS: Behavioral testing showed a significant improvement in pain threshold, incapacitance, and gait following an injection of ASA. MicroCT showed significant improvements in cartilage thickness and attenuation at day 10 only, and histology showed no detrimental effects compared to the vehicle control at day 21. Synovial fluid analysis showed a significant increase in anti-inflammatory IL-10. The safety cohort showed no significant differences except for an increase in synovitis at day 21, which could be evidence of a xenogeneic response in this model. CONCLUSIONS: In this study, an injection of ASA was well tolerated with no adverse events. Improvements in pain and function, along with cartilage properties at day 10, were observed. Increases in anti-inflammatory cytokines was also seen, along with no significant cartilage degeneration at day 21 compared to the vehicle control. This study provides evidence for the use of ASA as a nonsurgical treatment for knee OA. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13075-022-02750-9. BioMed Central 2022-03-04 2022 /pmc/articles/PMC8895852/ /pubmed/35246217 http://dx.doi.org/10.1186/s13075-022-02750-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Kimmerling, Kelly A.
Gomoll, Andreas H.
Farr, Jack
Mowry, Katie C.
Amniotic suspension allograft improves pain and function in a rat meniscal tear-induced osteoarthritis model
title Amniotic suspension allograft improves pain and function in a rat meniscal tear-induced osteoarthritis model
title_full Amniotic suspension allograft improves pain and function in a rat meniscal tear-induced osteoarthritis model
title_fullStr Amniotic suspension allograft improves pain and function in a rat meniscal tear-induced osteoarthritis model
title_full_unstemmed Amniotic suspension allograft improves pain and function in a rat meniscal tear-induced osteoarthritis model
title_short Amniotic suspension allograft improves pain and function in a rat meniscal tear-induced osteoarthritis model
title_sort amniotic suspension allograft improves pain and function in a rat meniscal tear-induced osteoarthritis model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8895852/
https://www.ncbi.nlm.nih.gov/pubmed/35246217
http://dx.doi.org/10.1186/s13075-022-02750-9
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