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Systematic Review of the Preclinical Technology Readiness of Orthopedic Gene Therapy and Outlook for Clinical Translation. | LitMetric

AI Article Synopsis

  • - Bone defects and poor fracture healing represent a growing health issue, with gene therapy emerging as a promising method for improving bone regeneration; however, existing studies mainly focus on small animal models, which don't fully mimic complex fracture conditions.
  • - Recent investigations into orthopedic gene therapy in large animal models show generally positive results, but methodological inconsistencies make comparisons challenging, and critical factors for clinical application are often overlooked.
  • - The review emphasizes the need for improved methodologies and comprehensive safety data to facilitate the clinical translation of gene therapy for bone repair, while outlining current research efforts and suggesting ways to address existing gaps.

Article Abstract

Bone defects and improper healing of fractures are an increasing public health burden, and there is an unmet clinical need in their successful repair. Gene therapy has been proposed as a possible approach to improve or augment bone healing with the potential to provide true functional regeneration. While large numbers of studies have been performed or in small animal models that support the use of gene therapy for bone repair, these systems do not recapitulate several key features of a critical or complex fracture environment. Larger animal models are therefore a key step on the path to clinical translation of the technology. Herein, the current state of orthopedic gene therapy research in preclinical large animal models was investigated based on performed large animal studies. A summary and an outlook regarding current clinical studies in this sector are provided. It was found that the results found in the current research literature were generally positive but highly methodologically inconsistent, rendering a comparison difficult. Additionally, factors vital for translation have not been thoroughly addressed in these model systems, and the risk of bias was high in all reviewed publications. These limitations directly impact clinical translation of gene therapeutic approaches due to lack of comparability, inability to demonstrate non-inferiority or equivalence compared with current clinical standards, and lack of safety data. This review therefore aims to provide a current overview of ongoing preclinical and clinical work, potential bottlenecks in preclinical studies and for translation, and recommendations to overcome these to enable future deployment of this promising technology to the clinical setting.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8011540PMC
http://dx.doi.org/10.3389/fbioe.2021.626315DOI Listing

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