Winearls C G, Fabre J W, Millard P R, Morris P J
Transplantation. 1979 Oct;28(4):271-4. doi: 10.1097/00007890-197910000-00001.
Cyclophosphamide was tested for its interaction with passive enhancement in suppressing the rejection of kidney allografts in the (DA x Lewis)F1 to Lewis rat strain. Dose response studies with cyclophosphamide showed that 10 mg/kg/day for 14 days was necessary for complete suppression of rejection and indefinite graft survival. Doses of 5 and 3.5 mg/kg/day had only a marginal effect on graft function and survival, although the lymphocytotoxin response to the graft was completely or very substantially suppressed by these smaller doses. The use of passive enhancement with cyclophosphamide at the 5- and 3.5-mg/kg/day doses resulted in a favourable interaction with improved graft function and survival. Interestingly, passive enhancement in combination with 5 mg/kg/day of cyclophosphamide resulted in indefinite graft survival only if cyclophosphamide was given for 28 days. If cyclophosphamide was given for 14 days, rejection was suppressed only during the period of cyclophosphamide treatment.
对环磷酰胺与被动增强作用在抑制(DA×Lewis)F1到Lewis大鼠品系肾移植排斥反应中的相互作用进行了测试。环磷酰胺的剂量反应研究表明,连续14天每天给予10mg/kg对于完全抑制排斥反应和实现移植肾长期存活是必要的。每天给予5mg/kg和3.5mg/kg的剂量对移植肾功能和存活仅有轻微影响,尽管这些较小剂量能完全或非常显著地抑制对移植肾的淋巴细胞毒素反应。在每天5mg/kg和3.5mg/kg剂量下使用环磷酰胺联合被动增强作用,可产生有利的相互作用,改善移植肾功能和存活。有趣的是,仅当给予环磷酰胺28天时,被动增强作用与每天5mg/kg环磷酰胺联合使用才会导致移植肾长期存活。如果给予环磷酰胺14天,则仅在环磷酰胺治疗期间抑制排斥反应。