Immunological and histological evaluation of decellularized allograft in a pig model: comparison with cryopreserved allograft

J Heart Valve Dis. 2004 Nov;13(6):984-90.

Abstract

Background and aim of the study: The remodeling process of the decellularized allograft after implantation remains unclear. Herein, the hemodynamics, recellularization and immunological response of the decellularized allograft were evaluated at four weeks after implantation in a mini-pig model, and compared with a cryopreserved allograft.

Methods: Six porcine pulmonary allografts were harvested from mini-pigs, and cryopreserved for four weeks. In two pigs, the grafts were decellularized with Triton X solution, after which static reseeding of the valve surface was performed for 48 h with autologous endothelial cells harvested from a leg artery. Decellularization, but not reseeding, was carried out in two mini-pigs, and cryopreservation alone in two mini-pigs. Whilst under right heart bypass, the right ventricular outflow tract was replaced in six minipigs. The grafts were explanted after four weeks; analysis included direct pressure measurement, echocardiography, macroscopy, light microscopy with hematoxylin and eosin staining, and immunohistochemical studies to identify macrophages, T lymphocytes, and endothelial cells.

Results: Hemodynamically and macroscopically, there were no major differences between the three groups. In the cryopreservation-only group, immunohistochemistry showed an influx of macrophages, and T lymphocytes at the cusps. Endothelial cell coverage was found in the decellularized and decellularized + cell-seeded groups, but no macrophages and T lymphocytes were found at the cusps.

Conclusion: Decellularization of the cryopreserved allograft may reduce the inflammatory response and improve its long-term durability.

Publication types

  • Comparative Study
  • Evaluation Study

MeSH terms

  • Animals
  • Cell Culture Techniques
  • Cryopreservation*
  • Echocardiography
  • Endothelial Cells / metabolism
  • Immunohistochemistry
  • Inflammation
  • Models, Animal
  • Pulmonary Valve / cytology
  • Pulmonary Valve / immunology
  • Pulmonary Valve / pathology
  • Pulmonary Valve / transplantation*
  • Pulmonary Valve Insufficiency / diagnostic imaging
  • Pulmonary Valve Insufficiency / physiopathology
  • Pulmonary Wedge Pressure
  • Swine
  • Swine, Miniature*
  • Tissue Transplantation
  • Transplantation, Homologous