Short-course immunosuppression using FK506 for rat tracheal allografts

Citation
M. Hashimoto et al., Short-course immunosuppression using FK506 for rat tracheal allografts, J CARD SURG, 41(3), 2000, pp. 487-492
Citations number
14
Categorie Soggetti
Cardiovascular & Respiratory Systems
Journal title
JOURNAL OF CARDIOVASCULAR SURGERY
ISSN journal
00219509 → ACNP
Volume
41
Issue
3
Year of publication
2000
Pages
487 - 492
Database
ISI
SICI code
0021-9509(200006)41:3<487:SIUFFR>2.0.ZU;2-S
Abstract
Background A minimizing immunosuppression after a tracheal allotransplantat ion is desirable. Methods. We examined the usefulness of a short-course of immunosuppression after tracheal allotransplantation in rat. Each transplant consisting of a 5-ring segment was heterotopically implanted into the omentum. Four animals underwent a syngeneic transplantation and thus served as controls (Group A ). Thirty animals underwent an allogeneic transplantation and were randomly classified into 4 groups as follows: No immunosupression (Group B, n=6), t reatment with 0.5 mg/kg of Tacrolims (FK506) (Group C, n=8), 1.0 mg/kg of F K506 (Group D, n=8), and 1.5 mg/kg of FK506 (Group E, n=8). Different doses of FK506 were administered intramuscularly for only three consecutive days after heterotopic tracheal allotransplantation. The serum levels of FK506 were then investigated 3, 7, 14, 21, and 28 days after transplantation in g roups C, D, and E. All rats were killed 28 days after transplantation and t hen the implanted tracheae were harvested, and evaluated histologically. Results. All animals survived for the protocol period. The graft morphology of Group E was significantly better than that of groups B, C, and D regard ing both macro- and microscopy, and also showed the same findings as that o f Group A, except for low-grade mononuclear cell infiltration. Only in Grou p E, the FK506 blood level was maintained at over 0.5 ng/ml which is the lo west detectable limit in this assay, until 21 days after transplantation. Conclusions. We thus conclude that 1.5 mg/kg of FK506 which was administere d for only three consecutive days after surgery may be used to maintain the morphology of tracheal allografts in rats for 28 days after transplantatio n.