Homan W P, French M E, Millard P, Denton T G, Fabre J W, Morris P J
Surgery. 1980 Jul;88(1):168-73.
Dose and time response studies of the new immunosuppressive agent, cyclosporin A, have been performed in a dog renal allograft model. Rejection of a renal allograft only occurred in one of six dogs receiving 20 mg/kg/day continuously, but in 10 of 11 dogs receiving 10 mg/kg/day. Doses of 10 or 20 mg/kg/day given for 2 or 3 weeks delayed rejection, but rejection occurred in all animals when the drug was stopped. This suggests that the drug does not produce clonal deletion of the lymphocytes engaged in the immune reaction against the graft, but merely their suppression. The histological picture of rejection was markedly improved by therapeutic doses of cyclosporin A. No consistent histological or biochemical evidence for heptatoxicity or nephrotoxicity was found even in the higher doses tested. One fatal and four non-fatal infectious complications were seen in 29 dogs receiving doses of 5 mg/kg/day or higher.
在犬肾移植模型中对新型免疫抑制剂环孢素A进行了剂量和时间反应研究。在持续接受20mg/kg/天的6只犬中,只有1只发生了肾移植排斥反应,但在接受10mg/kg/天的11只犬中有10只发生了排斥反应。给予10或20mg/kg/天的剂量持续2或3周可延迟排斥反应,但当停药时所有动物均发生了排斥反应。这表明该药物不会导致参与针对移植物免疫反应的淋巴细胞发生克隆清除,而只是对其产生抑制作用。环孢素A的治疗剂量可使排斥反应的组织学表现明显改善。即使在测试的较高剂量下,也未发现一致的肝毒性或肾毒性的组织学或生化证据。在接受5mg/kg/天或更高剂量的29只犬中,出现了1例致命和4例非致命的感染并发症。