Matrix-associated autologous chondrocyte transplantation in a compartmentalized early stage of osteoarthritis

Osteoarthritis Cartilage. 2013 Jan;21(1):217-25. doi: 10.1016/j.joca.2012.10.006. Epub 2012 Oct 17.

Abstract

Objective: Cartilage restoration in joints with an early stage of osteoarthritis (OA) is an important clinical challenge. In this study, a compartmentalized, early-stage OA was generated surgically in sheep stifle joints, and this model was used to evaluate a matrix-associated cell transplantation approach for cartilage repair.

Method: Eighteen sheep were operated twice. During the first operation, a unicompartmental OA in a stable joint was induced by creating a critical-size defect. The second operation served as a regeneration procedure. The eighteen sheep were divided into three groups. One group was treated with spongialization (SPONGIO), while the two others had spongialization followed by implantation of a hyaluronan matrix with (MACT) or without chondrocytes (MATRIX). The follow-up took place 4 months after the second operation. Gross Assessment of Joint Changes score and Brittberg score were used for the macroscopic evaluation, Mankin score, O'Driscoll score, and immunohistochemistry for collagen type I and type II for histological evaluation.

Results: The MACT group achieved significantly better results in both macroscopic and histological examinations. In the regeneration area, a Mankin score of 7.88 (6.20; 9.55) [mean (upper 95% confidence interval; lower 95% confidence interval)] was reached in the MACT group, 10.38 (8.03; 12.72) in the MATRIX group, and 10.33 (8.80; 11.87) in the SPONGIO group. The O'Driscoll score revealed a highly significant difference in the degree of defect repair: 15.92 (14.58; 17.25) for the MACT group compared to the two other groups [5.04 (1.21; 8.87) MATRIX and 6.58 (5.17; 8.00) SPONGIO; P < 0.0001].

Conclusion: This study demonstrates promising results toward the development of a biological regeneration technique for early-stage OA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arthritis, Experimental
  • Cartilage, Articular / pathology
  • Cartilage, Articular / surgery*
  • Cell Transplantation / methods*
  • Chondrocytes / transplantation*
  • Collagen Type I / metabolism
  • Collagen Type II / metabolism
  • Female
  • Hyaluronic Acid / therapeutic use
  • Osteoarthritis, Knee / pathology
  • Osteoarthritis, Knee / surgery*
  • Sheep
  • Stifle / surgery
  • Transplantation, Autologous / methods
  • Treatment Outcome
  • Viscosupplements / therapeutic use

Substances

  • Collagen Type I
  • Collagen Type II
  • Viscosupplements
  • Hyaluronic Acid