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Review
. 2024 Jan 25:12:1283752.
doi: 10.3389/fbioe.2024.1283752. eCollection 2024.

Protecting the regenerative environment: selecting the optimal delivery vehicle for cartilage repair-a narrative review

Affiliations
Review

Protecting the regenerative environment: selecting the optimal delivery vehicle for cartilage repair-a narrative review

T Mark Campbell et al. Front Bioeng Biotechnol. .

Abstract

Focal cartilage defects are common in youth and older adults, cause significant morbidity and constitute a major risk factor for developing osteoarthritis (OA). OA is the most common musculoskeletal (MSK) disease worldwide, resulting in pain, stiffness, loss of function, and is currently irreversible. Research into the optimal regenerative approach and methods in the setting of either focal cartilage defects and/or OA holds to the ideal of resolving both diseases. The two fundamentals required for cartilage regenerative treatment are 1) the biological element contributing to the regeneration (e.g., direct application of stem cells, or of an exogenous secretome), and 2) the vehicle by which the biological element is suspended and delivered. The vehicle provides support to the regenerative process by providing a protective environment, a structure that allows cell adherence and migration, and a source of growth and regenerative factors that can activate and sustain regeneration. Models of cartilage diseases include osteochondral defect (OCD) (which usually involve one focal lesion), or OA (which involves a more diffuse articular cartilage loss). Given the differing nature of these models, the optimal regenerative strategy to treat different cartilage diseases may not be universal. This could potentially impact the translatability of a successful approach in one condition to that of the other. An analogy would be the repair of a pothole (OCD) versus repaving the entire road (OA). In this narrative review, we explore the existing literature evaluating cartilage regeneration approaches for OCD and OA in animal then in human studies and the vehicles used for each of these two conditions. We then highlight strengths and challenges faced by the different approaches presented and discuss what might constitute the optimal cartilage regenerative delivery vehicle for clinical cartilage regeneration.

Keywords: cartilage; musculoskeletal health; osteoarthritis; regenerative therapy; stem cells.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

FIGURE 1
FIGURE 1
Graphical summary of scaffold types used in animal and clinical models of osteochondral defect and osteoarthritis. It can be seen that the proportion of engineered scaffolds is much larger in OCD models (animal models in particular), as compared to OA. OCD, osteochondral defect; OA, osteochondral defect.

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References

    1. Abdelhamid M. M., Eid G., Othman M. H. M., Ibrahim H., Elsers D., Elyounsy M., et al. (2023). The evaluation of cartilage regeneration efficacy of three-dimensionally biofabricated human-derived biomaterials on knee osteoarthritis: a single-arm, open label study in Egypt. J. Pers. Med. 13, 748. 10.3390/jpm13050748 - DOI - PMC - PubMed
    1. Ahmadian E., Eftekhari A., Janas D., Vahedi P. (2023). Nanofiber scaffolds based on extracellular matrix for articular cartilage engineering: a perspective. Nanotheranostics 7, 61–69. 10.7150/ntno.78611 - DOI - PMC - PubMed
    1. Akgun I., Unlu M. C., Erdal O. A., Ogut T., Erturk M., Ovali E., et al. (2015). Matrix-induced autologous mesenchymal stem cell implantation versus matrix-induced autologous chondrocyte implantation in the treatment of chondral defects of the knee: a 2-year randomized study. Arch. Orthop. Trauma Surg. 135, 251–263. 10.1007/s00402-014-2136-z - DOI - PubMed
    1. Al Faqeh H., Nor Hamdan B. M., Chen H. C., Aminuddin B. S., Ruszymah B. H. (2012). The potential of intra-articular injection of chondrogenic-induced bone marrow stem cells to retard the progression of osteoarthritis in a sheep model. Exp. Gerontol. 47, 458–464. 10.1016/j.exger.2012.03.018 - DOI - PubMed
    1. Anz A. W., Hubbard R., Rendos N. K., Everts P. A., Andrews J. R., Hackel J. G. (2020). Bone marrow aspirate concentrate is equivalent to platelet-rich plasma for the treatment of knee osteoarthritis at 1 Year: a prospective, randomized trial. Orthop. J. Sports Med. 8, 232596711990095. 10.1177/2325967119900958 - DOI - PMC - PubMed

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work is supported by funding from the Bruyère Academic Medical Organization Incentive Fund, The Ottawa Hospital Department of Medicine Translational Research Grant and the University of Ottawa Translational Research Grant.

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