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神经管缺陷后代的父母或经历自然流产的夫妇中人类白细胞抗原A、B相容性

HLA-A,B compatibility in parents of offspring with neural-tube defects or couples experiencing involuntary fetal wastage.

作者信息

Schacter B, Muir A, Gyves M, Tasin M

出版信息

Lancet. 1979 Apr 14;1(8120):796-9. doi: 10.1016/s0140-6736(79)91317-5.

DOI:10.1016/s0140-6736(79)91317-5
PMID:86041
Abstract

To test the contribution of a putative human analogue of the murine T locus to neural-tube defects (N.T.D.) and involuntary fetal wastage, HLA-A, B compatibility between husband and wife was studied in a group of 77 couples with known obstetric histories. The frequency of sharing of HLA-A,B antigens was significantly higher in 13 couples with recurrent fetal loss at one gestational age and in 11 couples whose offspring had had a lethal N.T.D. than in 17 couples with three or more normal pregnancies. The extent of HLA compatibility--that is, the number of antigens shared by husbands and wives--was significantly higher in 16 couples with one spontaneous abortion, 23 couples with recurrent spontaneous abortions, and 21 couples with N.T.D. offspring than in controls. These data are consistent with a contribution of a locus in or near the HLA complex to N.T.D. and involuntary fetal wastage.

摘要

为了检测假定的小鼠T位点的人类类似物对神经管缺陷(NTD)和自然流产的影响,在一组77对有已知产科病史的夫妇中研究了夫妻之间的HLA - A、B相容性。在13对在一个孕龄期有反复胎儿丢失的夫妇以及11对其后代患有致死性NTD的夫妇中,HLA - A、B抗原共享频率显著高于17对有三次或更多次正常妊娠的夫妇。在16对有一次自然流产、23对有反复自然流产以及21对有NTD后代的夫妇中,HLA相容性程度(即夫妻共享的抗原数量)显著高于对照组。这些数据与HLA复合体中或其附近的一个位点对NTD和自然流产有影响这一观点一致。

相似文献

1
HLA-A,B compatibility in parents of offspring with neural-tube defects or couples experiencing involuntary fetal wastage.神经管缺陷后代的父母或经历自然流产的夫妇中人类白细胞抗原A、B相容性
Lancet. 1979 Apr 14;1(8120):796-9. doi: 10.1016/s0140-6736(79)91317-5.
2
Parental HLA compatibility, fetal wastage and neural tube defects: evidence for a T/t-like locus in humans.父母的人类白细胞抗原相容性、胎儿流失与神经管缺陷:人类中存在类似T/t基因座的证据。
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Histocompatibility in couples with recurrent spontaneous abortion and normal fertility.复发性自然流产夫妇与正常生育夫妇的组织相容性
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引用本文的文献

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Human Leukocyte Antigen (HLA) Typing Study Identifies Maternal DQ2 Susceptibility Alleles among Infertile Women: Potential Associations with Autoimmunity and Micronutrients.人类白细胞抗原(HLA)分型研究确定了不孕女性中的母体DQ2易感等位基因:与自身免疫和微量营养素的潜在关联。
Nutrients. 2021 Sep 19;13(9):3270. doi: 10.3390/nu13093270.
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Microchimerism in women with recurrent miscarriage.复发性流产女性中的微嵌合体现象。
Chimerism. 2014;5(3-4):103-5. doi: 10.1080/19381956.2015.1017241. Epub 2015 Mar 16.
3
Microchimerism in recurrent miscarriage.
复发性流产中的微嵌合体现象。
Cell Mol Immunol. 2014 Nov;11(6):589-94. doi: 10.1038/cmi.2014.82. Epub 2014 Sep 22.
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The human T locus and spina bifida risk.人类T基因座与脊柱裂风险。
Hum Genet. 2004 Nov;115(6):475-82. doi: 10.1007/s00439-004-1185-8. Epub 2004 Sep 24.
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HLA and pregnancy: the paradox of the fetal allograft.人类白细胞抗原与妊娠:胎儿同种异体移植物的矛盾现象
Am J Hum Genet. 1998 Jan;62(1):1-5. doi: 10.1086/301692.
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Reproductive failure and the major histocompatibility complex.生殖失败与主要组织相容性复合体
Am J Hum Genet. 1995 Jun;56(6):1456-67.
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Absence of HLA association or linkage for variations in sensitivity to the odor of androstenone.雄烯酮气味敏感性变异不存在HLA关联或连锁。
Immunogenetics. 1982;15(6):579-89. doi: 10.1007/BF00347052.
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Parental HLA compatibility, fetal wastage and neural tube defects: evidence for a T/t-like locus in humans.父母的人类白细胞抗原相容性、胎儿流失与神经管缺陷:人类中存在类似T/t基因座的证据。
Am J Hum Genet. 1984 Sep;36(5):1082-91.
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Decreased HLA heterogeneity in parents of children with Down syndrome.唐氏综合征患儿父母的人类白细胞抗原(HLA)异质性降低。
Am J Hum Genet. 1983 Nov;35(6):1289-96.
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Androgenetic origin of African complete hydatidiform moles demonstrated by HLA markers.通过HLA标记物证实非洲完全性葡萄胎的雄激素起源。
Hum Genet. 1985;71(2):113-6. doi: 10.1007/BF00283364.