Thomson A W, Cameron I D
Scott Med J. 1981 Apr;26(2):139-44. doi: 10.1177/003693308102600210.
There have been no fundamental changes over the past 15 to 20 years in the immunosuppressive agents used in clinical transplantation. Equally efficient, but less toxic alternatives have been sought for some time. Cyclosporin A is an important new pharmacological immune suppressant, with a unique structure, which prolongs graft survival in a variety of species. It exerts a highly selective inhibitory effect on those T lymphocytes responding to antigenic challenge and is not myelotoxic. Indeed, no toxic effects have been reported at therapeutic doses in animals. Clinical trials indicate that it could prove extremely useful in management of graft rejection and autoimmune disease, however there are some doubts regarding possible hepatotoxic and nephrotoxic effects in man. There is also concern over the reported incidence of malignant lymphomas in cyclosporin A treated graft recipients.
在过去15到20年里,临床移植中使用的免疫抑制剂没有发生根本性变化。一段时间以来,人们一直在寻找同等有效但毒性较小的替代品。环孢素A是一种重要的新型药理免疫抑制剂,结构独特,可延长多种物种的移植物存活时间。它对那些对抗原刺激作出反应的T淋巴细胞具有高度选择性抑制作用,且无骨髓毒性。事实上,在动物的治疗剂量下未报告有毒性作用。临床试验表明,它在移植物排斥反应和自身免疫性疾病的治疗中可能非常有用,然而,对于其在人体中可能产生的肝毒性和肾毒性作用存在一些疑问。人们还对环孢素A治疗的移植物受者中报告的恶性淋巴瘤发病率表示担忧。