ABSTRACT
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 glycerin-preserved allograft groups. In contrast to the regenerated epithelium observed in autograft segments, all fresh allografts and glycerin-preserved 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.
Subject(s)
Animals , Dogs , Female , Male , Cryoprotective Agents , Glycerol , Graft Rejection/prevention & control , Respiratory Mucosa/immunology , Trachea/transplantation , Transplantation, Heterotopic/immunology , Cryopreservation/methods , Graft Rejection/immunology , Graft Rejection/pathology , Omentum/surgery , Organ Preservation/methods , Respiratory Mucosa/pathology , Trachea/immunology , Trachea/pathology , Transplantation, Heterotopic/pathologyABSTRACT
To investigate the pathogenesis of accelerated graft atherosclerosis after rdiac transplantation, a genetically well-defined and reproducible animal del is required. We performed heterotopic intraabdominal heart transplantation tween the two inbred strains of mice. Forty hearts from B10.A mice were ansplanted into B10.BR mice. Recipients were sacrificed at 1, 3, 5, 7, 14, 28, d 42 days after implantation. The specimens from both donor and recipient were amined with fluorescent immunohistochemistry and the serial histopathologic anges were evaluated. In the donor hearts, ICAM-1 and VCAM-1 expressions were nimal at day 1 and they gradually increased, reaching their peaks on day 5 or and remained unchanged by day 42. However, there were very little expressions the recipients' hearts. Mean percent areas of intima in the donor coronaries vealed progressive increase by day 42. However, those in the recipients cupied consistently less than 5% of the lumen. In conclusion, we demonstrated at a heterotopic murine heart transplantation model was a useful tool to oduce transplantation coronary artery disease and that adhesion molecules on e cardiac allografts were activated very early and remained elevated at all me-points, nonetheless the arterial lesion was detected after day 28 and its ogression was accelerated thereafter.
Subject(s)
Mice , Animals , Coronary Vessels/pathology , Heart Transplantation/pathology , Intercellular Adhesion Molecule-1/biosynthesis , Myocardium/pathology , Myocardium/metabolism , Time Factors , Transplantation, Heterotopic/pathology , Vascular Cell Adhesion Molecule-1/biosynthesisABSTRACT
El embarazo heterotópico es una entidad rara caracterizada por embarazo ectópico asociado a embarazo intrauterino. Su mayor incidencia se origina en la práctica creciente de la fertilización asistida. Aunque sobre este procedimiento se ejerce un adecuado seguimiento, ello no garantiza un diagnóstico fácil y oportuno