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Gene therapy in sports medicine.

作者信息

Lamsam C, Fu F H, Robbins P D, Evans C H

机构信息

Department of Orthopedic Surgery, University of Pittsburgh School of Medicine, Pennsylvania, USA.

出版信息

Sports Med. 1998 Feb;25(2):73-7. doi: 10.2165/00007256-199825020-00001.

DOI:10.2165/00007256-199825020-00001
PMID:9519397
Abstract

Sports injuries frequently involve tissues that have limited healing capabilities. In order to improve the healing process and thus prevent the serious consequences of injury, it is necessary to understand the molecular and cellular biology of healing. Several growth factors and other cytokines have been identified as important mediators of a successful healing process. Such molecules have promise as novel agents for the treatment of sporting injuries, but there is presently no clinically useful way to deliver them. Gene transfer may be used to serve this purpose. In this role, gene therapy functions as a type of local biological drug delivery system. Recent studies have shown the feasibility of transferring marker genes to synovium, chondrocytes, meniscal fibrochondrocytes, tenocytes and ligamental fibroblasts, prompting optimism about the eventual success of this approach.

摘要

相似文献

1
Gene therapy in sports medicine.
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本文引用的文献

1
Safety and effect of transforming growth factor-beta(2) for treatment of venous stasis ulcers.转化生长因子-β(2)治疗静脉淤滞性溃疡的安全性及疗效
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Repair of partial-thickness defects in articular cartilage: cell recruitment from the synovial membrane.关节软骨部分厚度缺损的修复:滑膜细胞募集
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In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector.慢病毒载体介导的非分裂细胞的体内基因递送与稳定转导
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9
Cellular immunity to viral antigens limits E1-deleted adenoviruses for gene therapy.针对病毒抗原的细胞免疫限制用于基因治疗的E1缺失型腺病毒。
Proc Natl Acad Sci U S A. 1994 May 10;91(10):4407-11. doi: 10.1073/pnas.91.10.4407.
10
Retroviral vectors for use in human gene therapy for cancer, Gaucher disease, and arthritis.用于人类癌症、戈谢病和关节炎基因治疗的逆转录病毒载体。
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