Heterotopic transplantation of glycerin-preserved trachea : effect of respiratory epithelium desquamation on acute rejection

An effective preservation method and decreased rejection are essential for tracheal transplantation in the reconstruction of large airway defects. Our objective in the present study was to evaluate the antigenic properties of glycerin-preserved tracheal segments. Sixty-one tracheal segments (2.4 to...

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Detalles Bibliográficos
Autores: Saueressig, Mauricio Guidi, Edelweiss, Maria Isabel Albano, Souza, Fabiano H., Moreschi, Alexandre Heitor, Savegnago, Fabrício L., Macedo Neto, Amarilio Vieira de
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2005
País:Brasil
Institución:Universidade Federal do Rio Grande do Sul (UFRGS)
Repositorio:Repositório Institucional da UFRGS
Idioma:portugués
OAI Identifier:oai:www.lume.ufrgs.br:10183/21186
Acceso en línea:http://hdl.handle.net/10183/21186
Access Level:acceso abierto
Palabra clave:Rejeição de enxerto
Traquéia
Transplante heterotópico
Glicerol
Mucosa respiratória
Graft rejection
Trachea
Transplantation
Glycerol
Respiratory mucosa
Descripción
Sumario:An effective preservation method and decreased rejection are essential for tracheal transplantation in the reconstruction of large airway defects. Our objective in the present study was to evaluate the antigenic properties of glycerin-preserved tracheal segments. Sixty-one tracheal segments (2.4 to 3.1 cm) were divided into three groups: autograft (N = 21), fresh allograft (N = 18) and glycerin-preserved allograft (N = 22). Two segments from different groups were implanted into the greater omentum of dogs (N = 31). After 28 days, the segments were harvested and analyzed for mononuclear infiltration score and for the presence of respiratory epithelium. The fresh allograft group presented the highest score for mononuclear infiltration (1.78 ± 0.43, P ≤ 0.001) when compared to the autograft and glycerinpreserved allograft groups. In contrast to the regenerated epithelium observed in autograft segments, all fresh allografts and glycerinpreserved allografts had desquamation of the respiratory mucosa. The low antigenicity observed in glycerin segments was probably the result of denudation of the respiratory epithelium and perhaps due to the decrease of major histocompatibility complex class II antigens.