Equine osteoarthritis: Strategies to enhance mesenchymal stromal cell-based acellular therapies

Front Vet Sci. 2023 Feb 10:10:1115774. doi: 10.3389/fvets.2023.1115774. eCollection 2023.

Abstract

Osteoarthritis (OA) is a degenerative disease that eventually leads to the complete degradation of articular cartilage. Articular cartilage has limited intrinsic capacity for self-repair and, to date, there is no curative treatment for OA. Humans and horses have a similar articular cartilage and OA etiology. Thus, in the context of a One Health approach, progress in the treatment of equine OA can help improve horse health and can also constitute preclinical studies for human medicine. Furthermore, equine OA affects horse welfare and leads to significant financial losses in the equine industry. In the last few years, the immunomodulatory and cartilage regenerative potentials of mesenchymal stromal cells (MSCs) have been demonstrated, but have also raised several concerns. However, most of MSC therapeutic properties are contained in their secretome, particularly in their extracellular vesicles (EVs), a promising avenue for acellular therapy. From tissue origin to in vitro culture methods, various aspects must be taken into consideration to optimize MSC secretome potential for OA treatment. Immunomodulatory and regenerative properties of MSCs can also be enhanced by recreating a pro-inflammatory environment to mimic an in vivo pathological setting, but more unusual methods also deserve to be investigated. Altogether, these strategies hold substantial potential for the development of MSC secretome-based therapies suitable for OA management. The aim of this mini review is to survey the most recent advances on MSC secretome research with regard to equine OA.

Keywords: acellular therapy; extracellular vesicles; horse; mesenchymal stromal cells; osteoarthritis.

Publication types

  • Review

Grants and funding

The publication of this review was supported by the European project OA-ACTIVE funded by the European Union within the frame-work of the Operational Programme ERDF (European Regional Development Funds)/ESF 2014−20. This work was also funded by an EQUISTEM ERDF grant, by Fonds Eperon (EQUISTEM), by the GIS CENTAURE-equine research (EQUISTEM-G), by ERDF and Regional Council of Basse-Normandie grant in the CPER CENTAURE program (2014–2020, CENTAURE Biotechnologies 2015 and CENTAURE PREACH 2016–17). MJ was supported by a Ph.D. scholarship from the Normandy Region Council (France) and the GIS CENTAURE-equine research (Nanovexstem project). RC was supported by a PhD fellowship co-financed by the Fonds Eperon and the Regional Council of Basse-Normandie. All the funding sources had absolutely no involvement in the study design, collection, analysis, and interpretation of data; in the writing of the manuscript; or in the decision to submit the manuscript for publication.