母胎HLA相容性的产前影响。

C Ober, J L Simpson, M Ward, R M Radvany, R Andersen, S Elias, R Sabbagha
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摘要

对特发性流产的回顾性研究和对正常夫妇的前瞻性研究都表明,共享HLA抗原的夫妇生育能力降低。然而,母胎组织相容性对存活胚胎的影响在很大程度上尚未得到研究。因此,我们前瞻性地研究了53名健康、有生育能力的妇女,她们的定时怀孕在受孕21天内被证实。测定HLA-A、-B和-DR位点抗原的母胎组织相容性状态。在妊娠8周、12周和20周时用超声监测胎儿生长速率。新生儿称重,测量(出生长,胸围,头围),并在分娩后72小时内由两位遗传学家中的一位以标准化的方式检查(116个主要和轻微异常)。尽管在HLA-A或HLA-B位点配型和不配型婴儿之间没有发现显著差异,但在HLA-DR配型和不配型婴儿的性别比例(p < 0.003)和轻微异常率(p < 0.05)上观察到显著差异。尽管在本样本中,HLA-DR相容婴儿和HLA-DR不相容婴儿的平均出生体重差异不显著,但HLA-DR相容婴儿比HLA-DR不相容婴儿平均小200克。我们将这些发现解释为在整个妊娠期间对组织相容性胎儿进行选择的证据,特别是在HLA-DR相容性方面。讨论了潜在的免疫和遗传机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prenatal effects of maternal-fetal HLA compatibility.

Both retrospective studies of idiopathic aborters, as well as prospective studies of normal couples, have shown reduced fertility among couples sharing HLA antigens. However, the effects of maternal-fetal histocompatibility on surviving embryos are largely univestigated. We thus prospectively studied 53 healthy, fertile women whose timed pregnancies were verified within 21 days of conception. Maternal-fetal histocompatibility status was determined for HLA-A,-B, and -DR locus antigens. Fetal growth rates were monitored by ultrasound at 8, 12, and 20 weeks gestation. Neonates were weighed, measured (birthlength, chest circumference, head circumference), and examined within 72 h of delivery (116 major and minor anomalies) in standardized fashion by one of two geneticists. Although no significant differences were found between infants compatible and incompatible at the HLA-A or HLA-B locus, significant differences were observed between HLA-DR compatible and incompatible infants for sex ratios (p less than .003) and minor anomaly rates (p less than .05). Although differences in mean birthweights between HLA-DR compatible and incompatible infants were not significant in this sample, HLA-DR compatible infants were on average 200 grams smaller than HLA-DR incompatible infants. We interpret these findings as evidence for selection against histocompatible fetuses throughout gestation, particularly with respect to HLA-DR compatibility. Potential immunologic and genetic mechanisms are discussed.

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