Revitalized and synovialized allograft for intrasynovial flexor tendon reconstruction in an in vivo canine model

ABSTRACT This study was to test our hypothesis that flexor tendon reconstruction with an allograft revitalized with bone marrow stromal cells (BMSCs) and synovialized with carbodiimide derivatized autologous synovial fluid (cd‐SYN) would result in better digit functional restoration than the convent...

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Published in:Journal of orthopaedic research Vol. 36; no. 8; pp. 2218 - 2227
Main Authors: Zhang, Tao, Lu, Cheng‐Chang, Reisdorf, Ramona L., Thoreson, Andrew R., Gingery, Anne, Moran, Steven L., Amadio, Peter C., Zhao, Chunfeng
Format: Journal Article
Language:English
Published: United States 01-08-2018
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Abstract ABSTRACT This study was to test our hypothesis that flexor tendon reconstruction with an allograft revitalized with bone marrow stromal cells (BMSCs) and synovialized with carbodiimide derivatized autologous synovial fluid (cd‐SYN) would result in better digit functional restoration than the conventional allograft tendon. A total of 32 flexor digital profundus tendons from the second and fifth digit of 16 dogs were created a repair failure model first. Then, failed‐repaired tendons were reconstructed with either a revitalized‐synovialized allograft tendon or a clinical standard autograft tendon (control group). The allograft tendon was seeded with autologous BMSCs in multiple slits and the graft surface was coated with cd‐SYN. A 6 weeks after tendon reconstruction, the digits were harvested and evaluated for digit function, adhesion status, tendon gliding resistance, attachment strength, cell viability, and histologic factors. The allograft group had significantly improved digit function compared with the control group through decreased work of flexion, increased digit range of motion under 2‐Newton force, and less adhesion score (p < .05). However, the distal attachment‐site strength and stiffness in the allograft tendon were significantly weaker than the autografts (p < .05). No significant difference was found for gliding resistance. Histologically, allograft tendons coated with allograft had smoother surfaces and showed tendon‐to‐bone and tendon‐to‐tendon incorporation. Viable BMSCs were found in the tendon slits 6 weeks after the graft. In conclusion, cellular lubricant‐based modification of allograft tendons improved digit function and reduced the adhesions compared with autograft for flexor tendon reconstruction. However, improvement of graft‐to‐host tendon healing is still challenging. © 2018 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 36:2218–2227, 2018.
AbstractList This study was to test our hypothesis that flexor tendon reconstruction with an allograft revitalized with bone marrow stromal cells (BMSCs) and synovialized with carbodiimide derivatized autologous synovial fluid (cd-SYN) would result in better digit functional restoration than the conventional allograft tendon. A total of 32 flexor digital profundus tendons from the second and fifth digit of 16 dogs were created a repair failure model first. Then, failed-repaired tendons were reconstructed with either a revitalized-synovialized allograft tendon or a clinical standard autograft tendon (control group). The allograft tendon was seeded with autologous BMSCs in multiple slits and the graft surface was coated with cd-SYN. A 6 weeks after tendon reconstruction, the digits were harvested and evaluated for digit function, adhesion status, tendon gliding resistance, attachment strength, cell viability, and histologic factors. The allograft group had significantly improved digit function compared with the control group through decreased work of flexion, increased digit range of motion under 2-Newton force, and less adhesion score (p < .05). However, the distal attachment-site strength and stiffness in the allograft tendon were significantly weaker than the autografts (p < .05). No significant difference was found for gliding resistance. Histologically, allograft tendons coated with allograft had smoother surfaces and showed tendon-to-bone and tendon-to-tendon incorporation. Viable BMSCs were found in the tendon slits 6 weeks after the graft. In conclusion, cellular lubricant-based modification of allograft tendons improved digit function and reduced the adhesions compared with autograft for flexor tendon reconstruction. However, improvement of graft-to-host tendon healing is still challenging. © 2018 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res.
ABSTRACT This study was to test our hypothesis that flexor tendon reconstruction with an allograft revitalized with bone marrow stromal cells (BMSCs) and synovialized with carbodiimide derivatized autologous synovial fluid (cd‐SYN) would result in better digit functional restoration than the conventional allograft tendon. A total of 32 flexor digital profundus tendons from the second and fifth digit of 16 dogs were created a repair failure model first. Then, failed‐repaired tendons were reconstructed with either a revitalized‐synovialized allograft tendon or a clinical standard autograft tendon (control group). The allograft tendon was seeded with autologous BMSCs in multiple slits and the graft surface was coated with cd‐SYN. A 6 weeks after tendon reconstruction, the digits were harvested and evaluated for digit function, adhesion status, tendon gliding resistance, attachment strength, cell viability, and histologic factors. The allograft group had significantly improved digit function compared with the control group through decreased work of flexion, increased digit range of motion under 2‐Newton force, and less adhesion score (p < .05). However, the distal attachment‐site strength and stiffness in the allograft tendon were significantly weaker than the autografts (p < .05). No significant difference was found for gliding resistance. Histologically, allograft tendons coated with allograft had smoother surfaces and showed tendon‐to‐bone and tendon‐to‐tendon incorporation. Viable BMSCs were found in the tendon slits 6 weeks after the graft. In conclusion, cellular lubricant‐based modification of allograft tendons improved digit function and reduced the adhesions compared with autograft for flexor tendon reconstruction. However, improvement of graft‐to‐host tendon healing is still challenging. © 2018 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 36:2218–2227, 2018.
Author Lu, Cheng‐Chang
Amadio, Peter C.
Zhao, Chunfeng
Reisdorf, Ramona L.
Thoreson, Andrew R.
Gingery, Anne
Zhang, Tao
Moran, Steven L.
Author_xml – sequence: 1
  givenname: Tao
  surname: Zhang
  fullname: Zhang, Tao
  organization: Jinan Central Hospital
– sequence: 2
  givenname: Cheng‐Chang
  surname: Lu
  fullname: Lu, Cheng‐Chang
  organization: Mayo Clinic
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  givenname: Ramona L.
  surname: Reisdorf
  fullname: Reisdorf, Ramona L.
  organization: Mayo Clinic
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  givenname: Andrew R.
  surname: Thoreson
  fullname: Thoreson, Andrew R.
  organization: Mayo Clinic
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  givenname: Anne
  surname: Gingery
  fullname: Gingery, Anne
  organization: Mayo Clinic
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  givenname: Steven L.
  surname: Moran
  fullname: Moran, Steven L.
  organization: Mayo Clinic
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  givenname: Peter C.
  surname: Amadio
  fullname: Amadio, Peter C.
  organization: Mayo Clinic
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  givenname: Chunfeng
  surname: Zhao
  fullname: Zhao, Chunfeng
  email: zhaoc@mayo.edu
  organization: Mayo Clinic
BackLink https://www.ncbi.nlm.nih.gov/pubmed/29575268$$D View this record in MEDLINE/PubMed
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Issue 8
Keywords bone marrow stromal cells
graft
tendon repair
surface modification
Language English
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Snippet ABSTRACT This study was to test our hypothesis that flexor tendon reconstruction with an allograft revitalized with bone marrow stromal cells (BMSCs) and...
This study was to test our hypothesis that flexor tendon reconstruction with an allograft revitalized with bone marrow stromal cells (BMSCs) and synovialized...
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SubjectTerms bone marrow stromal cells
graft
surface modification
tendon repair
Title Revitalized and synovialized allograft for intrasynovial flexor tendon reconstruction in an in vivo canine model
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjor.23889
https://www.ncbi.nlm.nih.gov/pubmed/29575268
https://search.proquest.com/docview/2018662601
Volume 36
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