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Cyclosporin a and tissue antigen matching in bone transplantation: Fibular allografts studied in the dog
19
Citations
35
References
1990
Year
EngineeringComposite AllograftImmunologyCyclosporin ATissue TransplantationSurgeryHistologic PropertiesBiomedical EngineeringOsteoporosisOrthopaedic SurgeryMetabolic KineticsBiomechanicsTissue AntigenBone RemodelingVascularized Bone GraftTransplantationVeterinary SurgeryBone TransplantationFibular AllograftsImmunosuppressive TherapyVeterinary ScienceMedicineGraft Rejection
We studied the mechanical, metabolic, and histologic properties of short-term nonvascularized cortical bone grafts in a canine fibular graft model. Sham operated nonvascularized autotransplanted and allotransplanted bones were compared. The allografts were performed between dog leukocyte antigen (DLA) class I and II matched; DLA class I and II mismatched; and cyclosporin A (CsA) treated, DLA class I and II mismatched animals. Cyclosporin was given for 1 month, and all the animals were followed for 3 months after surgery. Mechanical properties were investigated using standard torsional tests, metabolic kinetics were assessed using isotopic prelabeling techniques, and histomorphometric analysis of cross-sectional area properties and sequential fluorochrome labels were performed. Autografts were mechanically stronger and stiffer than all the types of allograft. CsA-treated, DLA-mismatched allografts performed better than matched allografts. These in turn were stronger than non-CsA-treated, mismatched allografts, which underwent nearly complete resorption. These relationships were preserved in the metabolic and histologic analyses. In this short-term animal study, although DLA matching resulted in a slight improvement in graft outcome, mismatched grafts in dogs receiving a short course of cyclosporin A fared even better.
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