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通过多孔缝线递送的结缔组织生长因子对滑膜内肌腱修复增殖阶段的影响。

Effect of connective tissue growth factor delivered via porous sutures on the proliferative stage of intrasynovial tendon repair.

作者信息

Linderman Stephen W, Shen Hua, Yoneda Susumu, Jayaram Rohith, Tanes Michael L, Sakiyama-Elbert Shelly E, Xia Younan, Thomopoulos Stavros, Gelberman Richard H

机构信息

Department of Orthopaedic Surgery, Washington University, 660 S. Euclid Avenue, Campus Box 8233, St. Louis, 63110, Missouri.

Department of Biomedical Engineering, Washington University, St. Louis, Missouri.

出版信息

J Orthop Res. 2018 Jul;36(7):2052-2063. doi: 10.1002/jor.23842. Epub 2018 Feb 1.

Abstract

Recent growth factor, cell, and scaffold-based experimental interventions for intrasynovial flexor tendon repair have demonstrated therapeutic potential in rodent models. However, these approaches have not achieved consistent functional improvements in large animal trials due to deleterious inflammatory reactions to delivery materials and insufficient induction of targeted biological healing responses. In this study, we achieved porous suture-based sustained delivery of connective tissue growth factor (CTGF) into flexor tendons in a clinically relevant canine model. Repairs with CTGF-laden sutures were mechanically competent and did not show any evidence of adhesions or other negative inflammatory reactions based on histology, gene expression, or proteomics analyses at 14 days following repair. CTGF-laden sutures induced local cellular infiltration and a significant biological response immediately adjacent to the suture, including histological signs of angiogenesis and collagen deposition. There were no evident widespread biological effects throughout the tendon substance. There were significant differences in gene expression of the macrophage marker CD163 and anti-apoptotic factor BCL2L1; however, these differences were not corroborated by proteomics analysis. In summary, this study provided encouraging evidence of sustained delivery of biologically active CTGF from porous sutures without signs of a negative inflammatory reaction. With the development of a safe and effective method for generating a positive local biological response, future studies can explore additional methods for enhancing intrasynovial tendon repair. © 2017 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 36:2052-2063, 2018.

摘要

近期,针对滑膜内屈肌腱修复的基于生长因子、细胞和支架的实验性干预措施在啮齿动物模型中已显示出治疗潜力。然而,由于对递送材料的有害炎症反应以及靶向生物愈合反应的诱导不足,这些方法在大型动物试验中并未实现一致的功能改善。在本研究中,我们在一个临床相关的犬类模型中实现了基于多孔缝线的结缔组织生长因子(CTGF)向屈肌腱的持续递送。用载有CTGF的缝线进行的修复在力学上是有效的,并且在修复后14天基于组织学、基因表达或蛋白质组学分析未显示出任何粘连或其他负面炎症反应的迹象。载有CTGF的缝线诱导了局部细胞浸润以及紧邻缝线处的显著生物学反应,包括血管生成和胶原沉积的组织学迹象。在整个肌腱实质中没有明显的广泛生物学效应。巨噬细胞标志物CD163和抗凋亡因子BCL2L1的基因表达存在显著差异;然而,这些差异未得到蛋白质组学分析的证实。总之,本研究提供了令人鼓舞的证据,表明从多孔缝线持续递送生物活性CTGF且无负面炎症反应迹象。随着一种安全有效的产生积极局部生物学反应方法的发展,未来的研究可以探索增强滑膜内肌腱修复的其他方法。© 2017骨科研究协会。由威利期刊公司出版。《矫形外科学研究》36:2052 - 2063,2018年。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9449/6013340/1fb4802c664b/nihms939751f1.jpg

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