环孢菌素A:遗传毒性及对人类生殖和发育的潜在不良影响综述

A.F. Olshan (Chair) , D.R. Mattison , T.S.B. Zwanenburg
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引用次数: 0

摘要

环孢菌素是移植受者和越来越多的自身免疫性疾病的重要治疗剂。实验动物和人类数据表明,环孢菌素不太可能具有遗传毒性。相反,硫唑嘌呤,一种经常与环孢菌素一起使用的药物,被认为具有遗传毒性,因此难以评估环孢菌碱的独立作用。环孢菌素似乎确实与动物和人类肿瘤(主要是淋巴瘤)的发展有关,但其潜在致癌性的基础尚不完全清楚。就生殖和发育毒性而言,环孢菌素对实验动物和人类都会产生一些不良影响。在动物身上,高剂量足以引起母体毒性。在人类中,已经注意到生长迟缓等结果,但肾毒性和由此产生的妊娠并发症的混杂影响使解释变得模糊。在样本量有限的人类研究中,尚未发现先天性畸形和遗传疾病的增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cyclosporine A: Review of genotoxicity and potential for adverse human reproductive and developmental effects

Cyclosporine is an important therapeutic agent for transplant recipients and for a growing number of autoimmune diseases. Experimental animal and human data has indicated that cyclosporine is unlikely to be genotoxic. In contrast, azathioprine, an agent often given with cyclosporine, is considered to be genotoxic making the assessment of the independent effects of cyclosporine difficult. Cyclosporine does appear to be related to the development of tumors, primarily lymphomas, in animals and humans, but the basis of its potential carcinogenicity is not completely understood. In terms of reproductive and developmental toxicity, cyclosporine produces some adverse effects in both experimental animals and humans. In animals, the effects are seen at high doses sufficient to cause maternal toxicity. In humans, outcomes such as growth retardation have been noted, but the confounding effects of renal toxicity and resultant pregnancy complications cloud the interpretation. An increase in congenital anomalies and genetic disease have not been found reported in human studies that are limited in sample size.

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