Winearls C G, Millard P R, Morris P J
Transplantation. 1978 May;25(5):229-34. doi: 10.1097/00007890-197805000-00001.
Passive enhancement provides only partial suppression of rejection in the (DA X Lewis)F1 to Lewis renal allograft model. Suboptimal (8 mg/kg/day) and supraoptimal (30 mg/kg/day) doses of azathioprine administered with enhancing serum failed to suppress the rejection reaction in enhanced animals. Similarly, suboptimal (4 mg/kg/day) and optimal (16 mg/kg/day) doses of methylprednisolone were ineffective. However, the onset of rejection in enhanced animals was delayed by the use of both azathioprine (30 mg/kg/day) and methylprednisolone (16 mg/kg/day). The survival times of enhanced animals treated with azathioprine were significantly shorter than those of animals treated with enhancing serum alone, suggesting that this agent may prevent the development of autoenhancement. Although suboptimal doses of antilymphocyte serum suppress rejection in this enhancement model, the dose requirements of conventional immunosuppressive agents appear to be maximal rather than minimal.
在(DA×Lewis)F1到Lewis肾移植模型中,被动增强仅能部分抑制排斥反应。与增强血清联合使用的次优剂量(8毫克/千克/天)和超优剂量(30毫克/千克/天)的硫唑嘌呤未能抑制增强动物的排斥反应。同样,次优剂量(4毫克/千克/天)和最佳剂量(16毫克/千克/天)的甲泼尼龙也无效。然而,使用硫唑嘌呤(30毫克/千克/天)和甲泼尼龙(16毫克/千克/天)均可延迟增强动物排斥反应的发生。接受硫唑嘌呤治疗的增强动物的存活时间显著短于仅接受增强血清治疗的动物,这表明该药物可能会阻止自身增强的发展。尽管次优剂量的抗淋巴细胞血清在这种增强模型中可抑制排斥反应,但传统免疫抑制剂的剂量需求似乎是最大剂量而非最小剂量。