Long-term Evaluation of Meniscal Tissue Formation in 3-dimensional–Printed Scaffolds With Sequential Release of Connective Tissue Growth Factor and TGF-β3 in an Ovine Model

Yusuke Nakagawa, Lisa A. Fortier, Jeremy J. Mao, Chang Hun Lee, Margaret B. Goodale, Matthew F. Koff, Tyler J. Uppstrom, Brett Croen, Susumu Wada, Camila B. Carballo, Hollis G. Potter, Scott A. Rodeo

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34 Citations (Scopus)

Résumé

Background: Artificial meniscal scaffolds are being developed to prevent development of osteoarthritis after meniscectomy. Previously, it was reported that 3-dimensional (3D) anatomic scaffolds loaded with connective tissue growth factor (CTGF) and transforming growth factor β3 (TGF-β3) achieved meniscal regeneration in an ovine model. This was a relatively short-term study (3 months postoperative), and outcome analyses did not include magnetic resonance imaging (MRI). Purpose: To evaluate long-term outcome of meniscal replacement with growth factor–laden poly-ε-caprolactone (PCL) scaffolds. Study Design: Controlled laboratory study. Methods: Anatomically shaped ovine meniscal scaffolds were fabricated from PCL with a 3D printer based on MRI data. Skeletally mature sheep (N = 34) were randomly allocated to 3 groups: scaffold without growth factor (0-µg group), scaffold with CTGF microspheres (µS) (5 µg) + TGF-β3 µS (5 µg) (5-µg group), and scaffold with CTGF µS (10 µg) + TGF-β3 µS (10 µg) (10-µg group). Unilateral medial meniscal replacement was performed. Animals were euthanized at 6 or 12 months. Regenerated meniscus, articular cartilage status, and synovial reaction were evaluated quantitatively with gross inspection, histology, and MRI. Kruskal-Wallis and Dunn tests were used to compare the 3 groups. Results: Remnants of the PCL scaffold were evident in the 6-month specimens and were decreased but still present at 12 months in most animals. There were no significant differences among groups in gross inspection, histology, or MRI for either meniscal regeneration or articular cartilage protection. All experimental groups exhibited articular cartilage degeneration as compared with control (nonoperated). In terms of synovitis, there were no clear differences among groups, suggesting that growth factors did not increase inflammation and fibrosis. MRI revealed that meniscal extrusion was observed in most animals (82.7%). Conclusion: Previously, the combination of CTGF and TGF-β3 was shown to stimulate mesenchymal stem cells into a fibrochondrocyte lineage. CTGF and TGF-β3 did not aggravate synovitis, suggesting no adverse response to the combination of 3D-printed PCL scaffold combined with CTGF and TGF-β3. Further work will be required to improve scaffold fixation to avoid meniscal extrusion. Clinical Relevance: A significant advantage of this technique is the ability to print custom-fit scaffolds from MRI-generated templates. In addition, average-size menisci could be printed and available for off-the-shelf applications. Based on the 1-year duration of the study, the approach appears to be promising for meniscal regeneration in humans.

Langue d'origineEnglish
Pages (de-à)2596-2607
Nombre de pages12
JournalAmerican Journal of Sports Medicine
Volume47
Numéro de publication11
DOI
Statut de publicationPublished - sept. 1 2019

Financement

The authors acknowledge with thanks the important technical assistance of Ying Liang (Orthopaedic Soft Tissue Research Program, Hospital for Special Surgery) for preparing histological specimens; Sarah Pownder, DVM, PhD (Department of Radiology, Hospital for Special Surgery) for MRI; Michelle Delco, DVM, PhD (Cornell University) for surgery; and Solaiman Tarafder (Columbia University) for preparing scaffolds. The authors also recognize the valuable support of Amir Lebaschi, MD, Colin Danaher, Daniel Nemirov, Samuel Green, and Joo Young Sunwoo (Orthopaedic Soft Tissue Research Program, Hospital for Special Surgery) for histological analysis.

Bailleurs de fondsNuméro du bailleur de fonds
Department of Radiology
Joo Young Sunwoo
National Institute of Arthritis and Musculoskeletal and Skin DiseasesR01AR065023
Cornell University

    ASJC Scopus Subject Areas

    • Physical Therapy, Sports Therapy and Rehabilitation
    • Orthopedics and Sports Medicine

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