Biologic and mechanical aspects of tendon fibrosis after injury and repair

被引:34
作者
Graham, Jack G. [1 ]
Wang, Mark L. [1 ,2 ]
Rivlin, Michael [1 ,2 ]
Beredjiklian, Pedro K. [1 ,2 ]
机构
[1] Thomas Jefferson Univ, Dept Orthopaed Surg, Sidney Kimmel Med Sch, Philadelphia, PA 19107 USA
[2] Thomas Jefferson Univ, Rothman Inst, Hand Surg Div, Philadelphia, PA 19107 USA
关键词
Fibrosis; regeneration; scarring; tendon injury; DIGITAL FLEXOR TENDONS; STROMAL CELL TRANSPLANTS; FIBROBLAST-GROWTH-FACTOR; IN-VITRO; ADHESION FORMATION; CONTROLLED DELIVERY; GENE-EXPRESSION; SCAR FORMATION; FACTOR-BETA; COLLAGEN;
D O I
10.1080/03008207.2018.1512979
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Tendon injuries of the hand that require surgical repair often heal with excess scarring and adhesions to adjacent tissues. This can compromise the natural gliding mechanics of the flexor tendons in particular, which operate within a fibro-osseous tunnel system similar to a set of pulleys. Even combining the finest suture repair techniques with optimal hand therapy protocols cannot ensure predictable restoration of hand function in these cases. To date, the majority of research regarding tendon injuries has revolved around the mechanical aspects of the surgical repair (i.e. suture techniques) and postoperative rehabilitation. The central principles of treatment gleaned from this literature include using a combination of core and epitendinous sutures during repair and initiating motion early on in hand therapy to improve tensile strength and limit adhesion formation. However, it is likely that the best clinical solution will utilize optimal biological modulation of the healing response in addition to these core strategies and, recently, the research in this area has expanded considerably. While there are no proven additive biological agents that can be used in clinical practice currently, in this review, we analyze the recent literature surrounding cytokine modulation, gene and cell-based therapies, and tissue engineering, which may ultimately lead to improved clinical outcomes following tendon injury in the future.
引用
收藏
页码:10 / 20
页数:11
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