Department of Orthopaedic Surgery, Keck School of Medicine, University of Southern California, Los Angeles, CA, United States.
Rehabilitation Medicine Research Center, Mayo Clinic, Rochester, MN, United States.
Curr Gene Ther. 2018;18(3):154-170. doi: 10.2174/1566523218666180410152842.
Musculoskeletal conditions are a major public health problem. Approximately 66 million individuals seek medical attention for a musculoskeletal injury in the United States, with current medical costs being estimated at $873 billion annually. Despite advances in pharmaceuticals, implant materials and surgical techniques, there remains an unmet clinical need for successful treatment of challenging musculoskeletal injuries and pathologic conditions, particularly in the setting of compromised biological environments. Tissue engineering via gene therapy attempts to provide an alternative treatment strategy to address the deficits associated with conventional approaches. The transfer of specific target genes coding for proteins with therapeutic or regenerative properties to target cells and tissues in the disease environment allows for their sustained production and release specifically at the site of interest. The increasing reports of success with gene therapy-based treatments in the clinical management of a variety of diseases provide genuine optimism that similar methods can be adapted for mainstream clinical application in musculoskeletal disorders. In preclinical studies, gene therapy has been successfully used to treat cartilaginous, bone, skeletal muscle, tendon, ligament and intervertebral disk injuries. In addition, gene therapy is being assessed in clinical trials for its safety and therapeutic potential in osteoarthritis. This review will specifically address the clinical potential, preclinical data and future hurdles for gene therapy to be a viable clinical entity for the treatment of fracture nonunion and difficult bone repair scenarios, articular cartilage repair and osteoarthritis.
肌肉骨骼疾病是一个主要的公共卫生问题。大约有 6600 万人因肌肉骨骼损伤而在美国寻求医疗,目前每年的医疗费用估计为 8730 亿美元。尽管在药物、植入材料和手术技术方面取得了进展,但在成功治疗具有挑战性的肌肉骨骼损伤和病理状况方面,仍然存在未满足的临床需求,特别是在生物环境受损的情况下。基因治疗通过组织工程试图提供一种替代治疗策略,以解决与传统方法相关的缺陷。将具有治疗或再生特性的特定靶基因编码的蛋白质转移到疾病环境中的靶细胞和组织中,可以在感兴趣的部位特异性地持续产生和释放它们。基因治疗在各种疾病的临床管理中取得成功的报道越来越多,这确实让人乐观地认为,类似的方法可以适应肌肉骨骼疾病的主流临床应用。在临床前研究中,基因治疗已成功用于治疗软骨、骨、骨骼肌、肌腱、韧带和椎间盘损伤。此外,基因治疗正在临床试验中评估其在骨关节炎中的安全性和治疗潜力。这篇综述将专门讨论基因治疗作为治疗骨折不愈合和困难骨修复、关节软骨修复和骨关节炎的可行临床实体的临床潜力、临床前数据和未来障碍。