Nishida K, Gilbertson L G, Robbins P D, Evans C H, Kang J D
Musculoskeletal Research Center, Department of Orthopaedic Surgery, University of Pittsburgh, PA 15213, USA.
Clin Orthop Relat Res. 2000 Oct(379 Suppl):S234-41. doi: 10.1097/00003086-200010001-00031.
Gene therapy involves the transfer of genes to cells such that the recipient cells express these genes and thereby synthesize the ribonucleic acid and protein that they encode. Recent investigations suggest that gene therapy may have potential applications in the treatment of intervertebral disc disorders, particularly those associated with disc degeneration. The successful in vivo transfer of therapeutic genes to target cells within the intervertebral disc in clinically relevant animal models is one example of the rapid progress that is being made. The purpose of the current review is to address several important technical issues, including choice of vectors and gene delivery strategy and the characteristics of the target tissues, which are relevant to future clinical applications of gene therapy for the treatment of intervertebral disc disorders. It already is apparent from the growing literature that gene therapy has the potential of becoming a valuable clinical treatment mode for intervertebral disc disorders in the twenty-first century.
基因治疗涉及将基因转移到细胞中,使受体细胞表达这些基因,从而合成它们所编码的核糖核酸和蛋白质。最近的研究表明,基因治疗在治疗椎间盘疾病,尤其是与椎间盘退变相关的疾病方面可能具有潜在应用。在临床相关动物模型中,将治疗性基因成功地体内转移到椎间盘内的靶细胞就是正在取得的快速进展的一个例子。本综述的目的是探讨几个重要的技术问题,包括载体的选择、基因递送策略以及靶组织的特征,这些问题与基因治疗在治疗椎间盘疾病的未来临床应用相关。从不断增加的文献中已经可以明显看出,基因治疗有潜力在21世纪成为治疗椎间盘疾病的一种有价值的临床治疗模式。