scholarly journals James Southard, PhD, Professor of Surgery (Emeritus), Pioneer in Organ Preservation, Co-inventor, UW Organ Preservation Solution

2020 ◽  
Vol 104 (9) ◽  
pp. 1764-1766 ◽  
Author(s):  
James H. Southard
2010 ◽  
Vol 139 (4) ◽  
pp. 1048-1056 ◽  
Author(s):  
Sivakkanan Loganathan ◽  
Tamás Radovits ◽  
Kristóf Hirschberg ◽  
Sevil Korkmaz ◽  
Achim Koch ◽  
...  

1997 ◽  
Vol 29 (8) ◽  
pp. 3539-3540 ◽  
Author(s):  
N. Baldan ◽  
M. Toffano ◽  
R. Cadrobbi ◽  
L. Codello ◽  
F. Calabrese ◽  
...  

1997 ◽  
Vol 25 (4) ◽  
pp. 407-416 ◽  
Author(s):  
Y. Funakoshi ◽  
S. Fujita ◽  
S. Fuchinoue ◽  
T. Agishi ◽  
K. Ota

2020 ◽  
pp. 000348942095735
Author(s):  
Pengcheng Cui ◽  
Pengfei Liu ◽  
Shuqin Li ◽  
Ruina Ma

Objectives: Reconstruction of long segmental tracheal defects is difficult because no ideal tracheal substitutes are currently available. Tracheal allotransplantation maintains cartilage and epithelium viability but requires immunosuppression because of epithelial immunogenicity. We aimed to obtain an epithelium-decellularized allograft that maintains cartilage viability and to evaluate long-term outcomes of such allografts implanted on dog backs without immunosuppressants. Methods: Twenty-five tracheas harvested from mongrel dogs were used to explore the period of epithelium decellularization by combined use of 1% sodium dodecyl sulfate and an organ preservation solution and to assess the chondrocyte viability and immunogenicity of the tracheas after decellularization. Sixteen epithelium-decellularized tracheal allografts and 10 fresh tracheal segments (6 cm long) were implanted in 26 beagles for durations of 10 days and 1, 3, 6, and 12 months. Macroscopic and microscopic examinations were used to evaluate the morphology, viability, and immune rejection of the allografts. Safranin-O staining was used to detect glycosaminoglycans. Results: The epithelium disappeared after 24 hours of decellularization. At 72 hours, almost no nuclei remained in the mucosa, while the mean survival rate of chondrocytes was 88.1%. Histological analysis demonstrated that the allograft retained intact tracheal rings and viable cartilage after heterotopic implantation for 1 year, with no immunological rejection. There were no significant differences in the glycosaminoglycan contents among the implanted epithelium-decellularized allografts. Conclusions: Epithelium-decellularized tracheal allografts with chondrocyte viability can be achieved by combined use of a detergent and organ preservation solution, which showed satisfactory cartilage viability and structural integrity after long-term heterotopic transplantation. Further studies on orthotopic transplantation are needed to assess the feasibility of allografts in reconstructing long segmental tracheal defects.


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