Suppr超能文献

基因治疗在骨质疏松性骨折愈合中的潜力。

The potential of gene therapy for fracture healing in osteoporosis.

作者信息

Egermann M, Schneider E, Evans C H, Baltzer A W

机构信息

AO Research Institute, Davos, Switzerland.

出版信息

Osteoporos Int. 2005 Mar;16 Suppl 2:S120-8. doi: 10.1007/s00198-004-1817-9. Epub 2005 Jan 15.

Abstract

Osteoporosis-associated fractures impair a patient's function and quality of life and represent one of the major public health burdens. Demographic changes predict a dramatic increase in osteoporotic fractures. Experimental data have shown that osteoporosis impairs fracture healing. Clinical observations demonstrate high failure rates of implant fixation in osteoporosis. The reduced healing capacity, including impaired bone formation, in osteoporotic humans might be due to defects in mesenchymal stem cells that lead to reduced proliferation and osteoblastic differentiation. Growth factors show remarkable promise as agents that can improve the healing of bone or increase the proliferation and differentiation capacities of mesenchymal stem cells. Their clinical utility is limited by delivery problems. The attraction of gene-transfer approaches is the unique ability to deliver authentically processed gene products to precise anatomical locations at therapeutic levels for sustained periods of time. Unlike the treatment of chronic diseases, it is neither necessary nor desirable for transgene expression to persist beyond the few weeks or months needed to achieve healing. This review presents different approaches of gene therapy to enhance fracture healing and summarizes the promising results of preclinical studies. It focuses on applications of this new technique to fracture healing in osteoporosis. In our opinion, these applications represent some of the few examples in which gene therapy has a good chance of early clinical success.

摘要

骨质疏松症相关骨折会损害患者的功能和生活质量,是主要的公共卫生负担之一。人口结构变化预示着骨质疏松性骨折将急剧增加。实验数据表明,骨质疏松症会损害骨折愈合。临床观察显示,骨质疏松症患者植入物固定的失败率很高。骨质疏松症患者愈合能力下降,包括骨形成受损,可能是由于间充质干细胞缺陷导致增殖和向成骨细胞分化减少。生长因子作为能够促进骨愈合或增加间充质干细胞增殖和分化能力的药物,显示出显著的前景。它们的临床应用受到递送问题的限制。基因转移方法的吸引力在于能够将经过真实加工的基因产物以治疗水平持续递送至精确的解剖位置。与慢性病治疗不同,转基因表达在实现愈合所需的几周或几个月后持续存在既不必要也不可取。本综述介绍了增强骨折愈合的不同基因治疗方法,并总结了临床前研究的有前景的结果。它重点关注这项新技术在骨质疏松症骨折愈合中的应用。我们认为,这些应用是基因治疗有很大机会早期取得临床成功的少数例子。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验