TY - JOUR
T1 - Effect of connective tissue growth factor delivered via porous sutures on the proliferative stage of intrasynovial tendon repair
AU - Linderman, Stephen W.
AU - Shen, Hua
AU - Yoneda, Susumu
AU - Jayaram, Rohith
AU - Tanes, Michael L.
AU - Sakiyama-Elbert, Shelly E.
AU - Xia, Younan
AU - Thomopoulos, Stavros
AU - Gelberman, Richard H.
N1 - Publisher Copyright:
© 2017 Orthopaedic Research Society. Published by Wiley Periodicals, Inc.
PY - 2018/7
Y1 - 2018/7
N2 - 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.
AB - 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.
KW - CTGF
KW - connective tissue growth factor
KW - drug delivery
KW - flexor tendon
KW - porous suture
UR - http://www.scopus.com/inward/record.url?scp=85050621861&partnerID=8YFLogxK
U2 - 10.1002/jor.23842
DO - 10.1002/jor.23842
M3 - Article
C2 - 29266404
AN - SCOPUS:85050621861
SN - 0736-0266
VL - 36
SP - 2052
EP - 2063
JO - Journal of Orthopaedic Research
JF - Journal of Orthopaedic Research
IS - 7
ER -