Allograft ligament transplantation

Author:

Sabiston Paul1,Frank CY2,Lam Tack3,Shrïve Nigel4

Affiliation:

1. Joint Injury and Diseases Research Group, Faculty of Medicine

2. Joint Injury and Diseases Research Group, Faculty of Medicine, Department of Surgery, Division of Orthopaedics

3. Faculty of Engineering, Department of Civil Engineering, The University of Calgary, Calgary, Alberta, Canada

4. Joint Injury and Diseases Research Group, Faculty of Medicine, Faculty of Engineering, Department of Civil Engineering, The University of Calgary, Calgary, Alberta, Canada

Abstract

Our purpose in this investigation was to describe and compare several morphological, histological, vascular, and biochemical healing processes of allograft and autograft bone-medial collateral ligament-bone com plexes in a rabbit model. Forty-nine animals had their right medial collateral ligament complex replaced with a frozen allograft while 30 separate control animals each received a fresh autograft. Animals were sacrificed at 3, 6, 12, 24, or 48 weeks after transplantation for comparison of grafted with unoperated contralateral control complexes. Results demonstrate some recov ery of both allografts and autografts over time. Allo grafts generally showed slower recovery than auto grafts with more persistent abnormalities in gross ap pearances, increased cellularity (corresponding to increased DNA content), and decreased collagen con tent. Allografts also showed aggressive remodeling of bone at insertions and they remained hypervascular throughout their substance as compared with contra lateral controls. Autografts went through similar but less chronic increases in cellularity and DNA concentra tion with no changes in collagen content. While both types of grafts showed some signs of "healing" and some recovery of control ligament biology, results are also consistent with allograft encasement, infiltration, and at least partial replacement by host tissue. This was particularly true of insertions. Collectively, these results also demonstrate some differences between allografts and autografts in this extraarticular model. The causes, mechanisms, and longer-term conse quences of these changes, including defining the qual ities of these graft and host tissues, clearly requires further investigation.

Publisher

SAGE Publications

Subject

Physical Therapy, Sports Therapy and Rehabilitation,Orthopedics and Sports Medicine

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1. TGF-β Family Signaling in Mesenchymal Differentiation;Cold Spring Harbor Perspectives in Biology;2017-05-15

2. Tendons and Ligaments: Tissue Engineering;Encyclopedia of Biomedical Polymers and Polymeric Biomaterials;2016-01-27

3. The dynamics of collagen uncrimping and lateral contraction in tendon and the effect of ionic concentration;Journal of Biomechanics;2013-09

4. Smad8/BMP2-engineered mesenchymal stem cells induce accelerated recovery of the biomechanical properties of the achilles tendon;Journal of Orthopaedic Research;2012-06-13

5. Basic Science and Injury of Muscle, Tendon, and Ligament;DeLee and Drez's Orthopaedic Sports Medicine;2010

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