Large Animal Models in Regenerative Medicine and Tissue Engineering: To Do or Not to Do

Iris Ribitsch(University of Veterinary Medicine Vienna), Pedro M. Baptista(Instituto de Investigación Sanitaria Aragón), Anna Lange-Consiglio(University of Milan), Luca Melotti(University of Padua), Marco Patruno(University of Padua), Florien Jenner(University of Veterinary Medicine Vienna), Eva Schnabl‐Feichter(University of Veterinary Medicine Vienna), Luke C. Dutton(Royal Veterinary College), David J. Connolly(University of Veterinary Medicine Vienna), Frank G. van Steenbeek(Utrecht University), Jayesh Dudhia(Royal Veterinary College), Louis C. Penning(Utrecht University)
Frontiers in Bioengineering and Biotechnology
August 13, 2020
Cited by 240Open Access
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Abstract

Rapid developments in Regenerative Medicine and Tissue Engineering has witnessed an increasing drive toward clinical translation of breakthrough technologies. However, the progression of promising preclinical data to achieve successful clinical market authorisation remains a bottleneck. One hurdle for progress to the clinic is the transition from small animal research to advanced preclinical studies in large animals to test safety and efficacy of products. Notwithstanding this, to draw meaningful and reliable conclusions from animal experiments it is critical that the species and disease model of choice is relevant to answer the research question as well as the clinical problem. Selecting the most appropriate animal model requires in-depth knowledge of specific species and breeds to ascertain the adequacy of the model and outcome measures that closely mirror the clinical situation. Traditional reductionist approaches in animal experiments, which often do not sufficiently reflect the studied disease, are still the norm and can result in a disconnect in outcomes observed between animal studies and clinical trials. To address these concerns a reconsideration in approach will be required. This should include a stepwise approach using in vitro and ex vivo experiments as well as in silico modeling to minimize the need for in vivo studies for screening and early development studies, followed by large animal models which more closely resemble human disease. Naturally occurring, or spontaneous diseases in large animals remain a largely untapped resource, and given the similarities in pathophysiology to humans they not only allow for studying new treatment strategies but also disease etiology and prevention. Naturally occurring disease models, particularly for longer lived large animal species, allow for studying disorders at an age when the disease is most prevalent. As these diseases are usually also a concern in the chosen veterinary species they would be beneficiaries of newly developed therapies. Improved awareness of the progress


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