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与母亲使用免疫抑制药物相关的胎儿生长迟缓。

Fetal growth retardation associated with maternal administration of immunosuppressive drugs.

作者信息

Scott J R

出版信息

Am J Obstet Gynecol. 1977 Jul 15;128(6):668-76. doi: 10.1016/0002-9378(77)90215-0.

Abstract

Since maternal-fetal immunogenetic disparity facilitates growth of the fetoplacental unit, nonspecific depression of the maternal immune system by immunosuppressive drugs could result in previously unrecognized adverse effects such as fetal growth retardation. To test this hypothesis, groups of 6 to 8 primigravid Fischer female rats mated with DA or Fischer male rats were treated with saline (controls) or either cyclophosphamide (Cytoxan) or azathioprine (Imuran) in doses similar to those used therapeutically in human subjects. It was found that these drugs caused an increased incidence of fetal death and produced fetal and neonatal growth retardation. Smaller placentas and fetuses reflected a decrease in cell number rather than cell size whereas water, fat, and protein content were only minimally affected. Analyses of mean maternal weight gain, spleen weight assays, and changes in the lymph nodes draining the uterus indicate that effects detrimental to the offspring are primarily the result of immunologic and cytotoxic mechanisms. Moreover, a review of the literature suggests that these immunosuppressive agents are also associated with small-for-gestational age infants in human pregnancies.

摘要

由于母胎免疫遗传差异有利于胎儿胎盘单位的生长,免疫抑制药物对母体免疫系统的非特异性抑制可能会导致以前未被认识到的不良影响,如胎儿生长受限。为了验证这一假设,将6至8只与DA或Fischer雄性大鼠交配的初孕Fischer雌性大鼠分为几组,分别用生理盐水(对照组)或环磷酰胺(癌得星)或硫唑嘌呤(依木兰)进行处理,所用剂量与人类治疗中使用的剂量相似。结果发现,这些药物导致胎儿死亡的发生率增加,并导致胎儿和新生儿生长受限。较小的胎盘和胎儿反映出细胞数量减少而非细胞大小减小,而水、脂肪和蛋白质含量仅受到轻微影响。对母体平均体重增加、脾脏重量测定以及子宫引流淋巴结变化的分析表明,对后代有害的影响主要是免疫和细胞毒性机制的结果。此外,文献综述表明,这些免疫抑制剂在人类妊娠中也与小于胎龄儿有关。

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