Lake K D, Canafax D M
Division of Cardiothoracic Transplantation and Research, Minneapolis Heart Institute Foundation, Abbott Northwestern Hospital, Minnesota 55407, USA.
J Antimicrob Chemother. 1995 Oct;36 Suppl B:11-22. doi: 10.1093/jac/36.suppl_b.11.
Solid organ transplant recipients depend on multiple immunosuppressive drugs, given in combination, to prevent rejection of their allografts. These patients often require many other therapeutic agents to treat underlying illnesses or concurrent diseases. Whenever a new medication is administered to a transplant patient, the potential exists for increasing or decreasing the tissue concentrations of immunosuppressive agents. This can lead to serious complications, such as over-immunosuppression and infection, under-immunosuppression and acute rejection, or additive toxicities, including nephrotoxicity. New immunosuppressants are under development and in clinical use, such as FK506, deoxyspergualin, OG 37-325, rapamycin, brequinar, and mycophenolate mofetil, thereby creating the possibility of many new drug-drug interactions.
实体器官移植受者依靠多种联合使用的免疫抑制药物来防止同种异体移植物的排斥反应。这些患者常常需要许多其他治疗药物来治疗基础疾病或并发疾病。每当给移植患者使用一种新药物时,就有可能增加或降低免疫抑制药物的组织浓度。这可能导致严重的并发症,如免疫抑制过度和感染、免疫抑制不足和急性排斥反应,或包括肾毒性在内的相加毒性。新的免疫抑制剂正在研发并用于临床,如FK506、脱氧精胍菌素、OG 37-325、雷帕霉素、布喹那和霉酚酸酯,从而产生了许多新的药物相互作用的可能性。