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Injury. 2011 Jun;42(6):599-604. doi: 10.1016/j.injury.2011.03.032. Epub 2011 Apr 13.
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本文引用的文献

1
Getting arthritis gene therapy into the clinic.将关节炎基因疗法推向临床。
Nat Rev Rheumatol. 2011 Apr;7(4):244-9. doi: 10.1038/nrrheum.2010.193. Epub 2010 Dec 7.
2
Efficacy of gene therapy for X-linked severe combined immunodeficiency.X 连锁严重联合免疫缺陷的基因治疗疗效。
N Engl J Med. 2010 Jul 22;363(4):355-64. doi: 10.1056/NEJMoa1000164.
3
Gene therapy for bone healing.基因治疗在骨愈合中的应用。
Expert Rev Mol Med. 2010 Jun 23;12:e18. doi: 10.1017/S1462399410001493.
4
Recapitulation of endochondral bone formation using human adult mesenchymal stem cells as a paradigm for developmental engineering.以人成体间充质干细胞为范例对软骨内骨形成的重述:发育工程学视角
Proc Natl Acad Sci U S A. 2010 Apr 20;107(16):7251-6. doi: 10.1073/pnas.1000302107. Epub 2010 Apr 6.
5
Viral vectors for gene transfer: current status of gene therapeutics.用于基因转移的病毒载体:基因治疗的现状
Handb Exp Pharmacol. 2010(197):143-70. doi: 10.1007/978-3-642-00477-3_5.
6
Autologous bone graft: properties and techniques.自体骨移植:特性与技术。
J Orthop Trauma. 2010 Mar;24 Suppl 1:S36-40. doi: 10.1097/BOT.0b013e3181cec4a1.
7
Gene therapy for fracture healing.基因治疗在骨折愈合中的应用。
J Orthop Trauma. 2010 Mar;24 Suppl 1:S17-24. doi: 10.1097/BOT.0b013e3181cec6fb.
8
Direct gene therapy for bone regeneration: gene delivery, animal models, and outcome measures.直接基因治疗骨再生:基因传递、动物模型和结果测量。
Tissue Eng Part B Rev. 2010 Feb;16(1):13-20. doi: 10.1089/ten.teb.2009.0156.
9
Use of genetically modified muscle and fat grafts to repair defects in bone and cartilage.利用基因修饰的肌肉和脂肪移植物修复骨和软骨的缺陷。
Eur Cell Mater. 2009 Dec 31;18:96-111. doi: 10.22203/ecm.v018a09.
10
Alipogene tiparvovec, an adeno-associated virus encoding the Ser(447)X variant of the human lipoprotein lipase gene for the treatment of patients with lipoprotein lipase deficiency.阿利泼金替帕罗韦克,一种编码人脂蛋白脂肪酶基因Ser(447)X变体的腺相关病毒,用于治疗脂蛋白脂肪酶缺乏症患者。
Curr Opin Mol Ther. 2009 Dec;11(6):681-91.

基因治疗在骨再生中的应用。

Gene therapy for the regeneration of bone.

机构信息

Center for Advanced Orthopaedic Studies, Department of Orthopaedic Surgery, Beth Israel Deaconess Medical Center, BIDMC-RN-115, 330, Brookline Avenue, Boston, MA 02215, United States.

出版信息

Injury. 2011 Jun;42(6):599-604. doi: 10.1016/j.injury.2011.03.032. Epub 2011 Apr 13.

DOI:10.1016/j.injury.2011.03.032
PMID:21489526
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3106986/
Abstract

Gene transfer technologies offer the prospect of enhancing bone regeneration by delivering osteogenic gene products locally to osseous defects. In most cases the gene product will be a protein, which will be synthesized endogenously within and around the lesion in a sustained fashion. It will have undergone authentic post-translational processing and lack the alterations that occur when recombinant proteins are synthesized in bioreactors and stored. Several different ex vivo and in vivo gene delivery strategies have been developed for this purpose, using viral and non-viral vectors. Proof of principle has been established in small animal models using a variety of different transgenes, including those encoding morphogens, growth factors, angiogenic factors, and transcription factors. A small number of studies demonstrate efficacy in large animal models. Developing these promising findings into clinical trials will be a long process, constrained by economic, regulatory and practical considerations. Nevertheless, the overall climate for gene therapy is improving, permitting optimism that applications in bone regeneration will eventually become available.

摘要

基因转移技术提供了通过局部递送成骨基因产物来增强骨再生的前景,用于骨缺损。在大多数情况下,基因产物将是一种蛋白质,它将在病变内和周围以持续的方式内源性合成。它将经历真正的翻译后加工,并且缺乏在生物反应器中合成和储存重组蛋白时发生的改变。已经开发了几种不同的用于此目的的体外和体内基因传递策略,使用病毒和非病毒载体。已经使用多种不同的转基因(包括编码形态发生素、生长因子、血管生成因子和转录因子的转基因)在小动物模型中建立了原理证明。少数研究表明在大型动物模型中的有效性。将这些有前途的发现开发成临床试验将是一个漫长的过程,受到经济、监管和实际考虑的限制。尽管如此,基因治疗的总体情况正在改善,这使得人们有理由乐观地认为,骨再生的应用最终将成为可能。