首页> 外文期刊>Clinical immunology: The official journal of the Clinical Immunology Society >Molecular genetic studies on the compatibility of HLA class II alleles in patients with unexplained recurrent miscarriage in the Japanese population.
【24h】

Molecular genetic studies on the compatibility of HLA class II alleles in patients with unexplained recurrent miscarriage in the Japanese population.

机译:关于日本人群无法解释的反复流产患者中HLA II类等位基因相容性的分子遗传学研究。

获取原文
获取原文并翻译 | 示例
           

摘要

It is hypothesized that patients having unexplained recurrent miscarriage lack an appropriate immune reaction against their partner's antigens, which means possible compatibility of HLA antigens between the patient couples. The conclusion, however, has not yet been achieved, so the purpose was to determine whether significant compatibility of HLA class II exists between the couples. The HLA-DRB1 and -DQB1 genotypes were determined using PCR-RFLP method in 91 patient couples and in 72 normal couples. The number of patient couples with zero-allele mismatch was not significantly different compared with that of control couples regarding HLA-DRB1 genotype and phenotype, as well as regarding HLA-DQB1 genotype and phenotype. While the number of patient couples with zero- and one-allele mismatch was significantly higher compared with that in control as to HLA-DR and -DQ phenotype (P=0.029 by Chi-square test). In conclusion, it is suggested that the compatibility of HLA class II antigens between couples might be involved in the genesis of unexplained recurrent miscarriage.
机译:假设患有无法解释的反复流产的患者缺乏针对其伴侣抗原的适当免疫反应,这意味着HLA抗原在患者夫妇之间可能具有相容性。但是,尚未得出结论,因此目的是确定夫妇之间是否存在HLA II类的显着兼容性。使用PCR-RFLP方法在91对患者对和72对正常对中确定了HLA-DRB1和-DQB1基因型。在HLA-DRB1基因型和表型以及HLA-DQB1基因型和表型方面,具有零等位基因错配的患者对的数量与对照组相比没有显着差异。尽管在HLA-DR和-DQ表型方面,零等位基因和一等位基因错配的患者夫妇的数量明显高于对照组(卡方检验,P = 0.029)。结论是,夫妻之间HLA II类抗原的相容性可能参与了无法解释的反复流产的发生。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号