Recombinant fibroblast growth factor‐18 (sprifermin) enhances microfracture‐induced cartilage healing

• Published in: Journal of orthopaedic research Vol. 40; no. 3; pp. 553 - 564
• Main Authors: Hendesi, Honey, Stewart, Suzanne, Gibison, Michelle L., Guehring, Hans, Richardson, Dean W., Dodge, George R.
• Format: Journal Article
• Language: English
• Published: United States 01.03.2022
• Subjects: Animals; cartilage repair; Cartilage, Articular - pathology; equine animal model; FGF‐18; Fibroblast Growth Factors - metabolism; Fibroblast Growth Factors - pharmacology; Fibroblast Growth Factors - therapeutic use; Fractures, Stress - drug therapy; Horses; Lameness, Animal - drug therapy; Lameness, Animal - metabolism; Lameness, Animal - pathology; microfracture; osteoarthritis; sprifermin; microfracture; equine animal model; FGF-18; cartilage repair; osteoarthritis; sprifermin
• ISSN: 0736-0266; 1554-527X
• DOI: 10.1002/jor.25063

Posttraumatic osteoarthritis is a disabling condition impacting the mostly young and active population. In the present study, we investigated the impact of intra‐articular sprifermin, a recombinant truncated fibroblast growth factor 18, on the outcome of microfracture treatment, a widely used surgical technique to enhance cartilage healing at the site of injury. For this study, we created a cartilage defect and performed microfracture treatment in fetlock joints of 18 horses, treated joints with one of three doses of sprifermin (10, 30, or 100 μg) or with saline, hyaluronan, and evaluated animals functional and structural outcomes over 24 weeks. For primary outcome measures, we performed histological evaluations and gene expression analysis of aggrecan, collagen types I and II, and cartilage oligomeric matrix protein in three regions of interest. As secondary outcome measures, we examined animals' lameness, performed arthroscopic, radiographic, and computed tomography (CT) scan imaging and gross morphology assessment. We detected the highest treatment benefit following 100 μg sprifermin treatment. The overall histological assessment showed an improvement in the kissing region, and the expression of constitutive genes showed a concentration‐dependent enhancement, especially in the peri‐lesion area. We detected a significant improvement in lameness scores, arthroscopic evaluations, radiography, and CT scans following sprifermin treatment when results from three dose‐treatment groups were combined. Our results demonstrated, for the first time, an enhancement on microfracture outcomes following sprifermin treatment suggesting a cartilage regenerative role and a potential benefit of sprifermin treatment in early cartilage injuries.