Homan W P, Fabre J W, Millard P R, Morris P J
Transplantation. 1980 Nov;30(5):354-7. doi: 10.1097/00007890-198011000-00009.
With the use of a DA to LEW rat renal allograft model, the ability of cyclosporin A to influence a second-set rejection was investigated. Sensitization of LEW rats was accomplished by performing DA to LEW skin grafts 4 to 5 weeks before kidney allografting. Cyclosporin A was given to sensitized rats in doses of 10 or 25 mg/kg/day for 14 days from the time of renal transplantation. Neither dose was nearly as effective in prolonging kidney graft survival in sensitized rats as the 10 mg/kg/day dose was in prolonging kidney graft survival in unsensitized rats. In the 25 mg/kg/day dose, cyclosporin A was capable of suppressing antibody formation to the graft in sensitized recipients despite the presence of donor-specific antibodies at the time of renal transplantation. The 10 mg/kg/day dose of cyclosporin A did not, however, suppress antibody formation after renal transplantation in sensitized recipients. In both sensitized and unsensitized rats cyclosporin A was effective in ameliorating the histological findings of arterial fibrinoid necrosis and glomerular necrosis in the renal allografts. In neither sensitized nor unsensitized rats did cyclosporin A effect the mononuclear cell infiltration of the renal allograft.
利用DA到LEW大鼠肾移植模型,研究了环孢素A影响二次排斥反应的能力。在肾移植前4至5周,通过进行DA到LEW皮肤移植使LEW大鼠致敏。从肾移植时起,以10或25mg/kg/天的剂量给致敏大鼠注射环孢素A,持续14天。在延长致敏大鼠肾移植存活时间方面,这两种剂量都远不如10mg/kg/天的剂量在延长未致敏大鼠肾移植存活时间时有效。在25mg/kg/天的剂量下,尽管肾移植时存在供体特异性抗体,但环孢素A仍能够抑制致敏受体中针对移植肾的抗体形成。然而,10mg/kg/天剂量的环孢素A在致敏受体肾移植后并未抑制抗体形成。在致敏和未致敏大鼠中,环孢素A均能有效改善肾移植中动脉纤维蛋白样坏死和肾小球坏死的组织学表现。在致敏和未致敏大鼠中,环孢素A均未影响肾移植中的单核细胞浸润。