Amniotic Suspension Allograft and Bone Marrow Aspirate Concentrate Results in Highly Variable Proinflammatory Cytokines in a Coculture Model of Osteoarthritis

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Main Authors: Charles P. Hannon, Navya Dandu, Hailey P. Huddleston, Divesh Sachdev, Neal B. Naveen, David Frisbie, Wayne McIlwraith, Arnavaz Hakimiyan, Brian J. Cole, Susanna Chubinskaya, Adam B. Yanke
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Published: Wiley 2026
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author Charles P. Hannon
Navya Dandu
Hailey P. Huddleston
Divesh Sachdev
Neal B. Naveen
David Frisbie
Wayne McIlwraith
Arnavaz Hakimiyan
Brian J. Cole
Susanna Chubinskaya
Adam B. Yanke
author_facet Charles P. Hannon
Navya Dandu
Hailey P. Huddleston
Divesh Sachdev
Neal B. Naveen
David Frisbie
Wayne McIlwraith
Arnavaz Hakimiyan
Brian J. Cole
Susanna Chubinskaya
Adam B. Yanke
Charles P. Hannon
Navya Dandu
Hailey P. Huddleston
Divesh Sachdev
Neal B. Naveen
David Frisbie
Wayne McIlwraith
Arnavaz Hakimiyan
Brian J. Cole
Susanna Chubinskaya
Adam B. Yanke
collection Wiley Open Access
contents Amniotic Suspension Allograft and Bone Marrow Aspirate Concentrate Results in Highly Variable Proinflammatory Cytokines in a Coculture Model of Osteoarthritis Charles P. Hannon Navya Dandu Hailey P. Huddleston Divesh Sachdev Neal B. Naveen David Frisbie Wayne McIlwraith Arnavaz Hakimiyan Brian J. Cole Susanna Chubinskaya Adam B. Yanke Arthroscopy Purpose To evaluate the anti‐inflammatory and disease‐modifying potential of bone marrow aspirate concentrate (BMAC) and amniotic suspension allograft (ASA) in a chondrocyte and synovium coculture model of osteoarthritis. Methods Seventeen patients were enrolled for cartilage, synovium, and bone marrow aspirate tissue donation prior to a total knee arthroplasty. Cartilage and synovium explants were cocultured into four different groups: one baseline group, one control group (96‐hour coculture), BMAC group, and ASA group. Interleukin‐1β (IL‐1β), interleukin‐6 (IL‐6), and tumor necrosis factor‐alpha (TNF‐α) were measured at 96 hours in the media with enzyme‐linked immunosorbent assay. Collagen type 1 α 1, Collagen type 2 α 2, Collagen type 3 α 1, aggrecan, and Cartilage Oligomeric Matrix Protein were measured in the cartilage and synovium by reverse transcription polymerase chain reaction. Safranin‐O staining were performed on all groups and scored by the modified Mankin scoring system. Results Samples treated with ASA showed a significantly lower concentration of IL‐1β when compared to control samples (11.2 ± 13.9 vs 20.2 ± 39.5 pg/mL, P  = .04). Treatment with BMAC was associated with a significantly lower concentrations of IL‐6 when compared to control samples (607.32 ± 271.07 vs 767.11 ± 30.84, P  = .02). No significant differences were observed in gene expression within chondrocytes and synoviocytes or for Mankin scoring between treatment and control groups. Conclusions Osteoarthritic chondrocytes and synovial tissue may respond to BMAC and ASA by a reduction in IL‐1β and IL‐6 concentrations, but short‐term cytokine responses are variable. The mechanism of response remains unknown. Clinical Relevance This study aims to reveal the mechanism of BMAC and ASA by which these biologics function in a model of an arthritic joint. 10.1002/arj.70021 http://onlinelibrary.wiley.com/termsAndConditions#vor
doi_str_mv 10.1002/arj.70021
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institution Wiley Open Access
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publishDate 2026
publisher Wiley
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spellingShingle Amniotic Suspension Allograft and Bone Marrow Aspirate Concentrate Results in Highly Variable Proinflammatory Cytokines in a Coculture Model of Osteoarthritis
Charles P. Hannon
Navya Dandu
Hailey P. Huddleston
Divesh Sachdev
Neal B. Naveen
David Frisbie
Wayne McIlwraith
Arnavaz Hakimiyan
Brian J. Cole
Susanna Chubinskaya
Adam B. Yanke
Arthroscopy
Amniotic Suspension Allograft and Bone Marrow Aspirate Concentrate Results in Highly Variable Proinflammatory Cytokines in a Coculture Model of Osteoarthritis Charles P. Hannon Navya Dandu Hailey P. Huddleston Divesh Sachdev Neal B. Naveen David Frisbie Wayne McIlwraith Arnavaz Hakimiyan Brian J. Cole Susanna Chubinskaya Adam B. Yanke Arthroscopy Purpose To evaluate the anti‐inflammatory and disease‐modifying potential of bone marrow aspirate concentrate (BMAC) and amniotic suspension allograft (ASA) in a chondrocyte and synovium coculture model of osteoarthritis. Methods Seventeen patients were enrolled for cartilage, synovium, and bone marrow aspirate tissue donation prior to a total knee arthroplasty. Cartilage and synovium explants were cocultured into four different groups: one baseline group, one control group (96‐hour coculture), BMAC group, and ASA group. Interleukin‐1β (IL‐1β), interleukin‐6 (IL‐6), and tumor necrosis factor‐alpha (TNF‐α) were measured at 96 hours in the media with enzyme‐linked immunosorbent assay. Collagen type 1 α 1, Collagen type 2 α 2, Collagen type 3 α 1, aggrecan, and Cartilage Oligomeric Matrix Protein were measured in the cartilage and synovium by reverse transcription polymerase chain reaction. Safranin‐O staining were performed on all groups and scored by the modified Mankin scoring system. Results Samples treated with ASA showed a significantly lower concentration of IL‐1β when compared to control samples (11.2 ± 13.9 vs 20.2 ± 39.5 pg/mL, P  = .04). Treatment with BMAC was associated with a significantly lower concentrations of IL‐6 when compared to control samples (607.32 ± 271.07 vs 767.11 ± 30.84, P  = .02). No significant differences were observed in gene expression within chondrocytes and synoviocytes or for Mankin scoring between treatment and control groups. Conclusions Osteoarthritic chondrocytes and synovial tissue may respond to BMAC and ASA by a reduction in IL‐1β and IL‐6 concentrations, but short‐term cytokine responses are variable. The mechanism of response remains unknown. Clinical Relevance This study aims to reveal the mechanism of BMAC and ASA by which these biologics function in a model of an arthritic joint. 10.1002/arj.70021 http://onlinelibrary.wiley.com/termsAndConditions#vor
title Amniotic Suspension Allograft and Bone Marrow Aspirate Concentrate Results in Highly Variable Proinflammatory Cytokines in a Coculture Model of Osteoarthritis
topic Arthroscopy
url https://arthroscopyjournals.onlinelibrary.wiley.com/doi/10.1002/arj.70021