Jin K, Ho H N, Speed T P, Gill T J
Department of Family Medicine, University of Pittsburgh School of Medicine, PA 15261, USA.
Am J Hum Genet. 1995 Jun;56(6):1456-67.
The association between HLA sharing and recurrent spontaneous abortion (RSA) was tested in 123 couples and the association between HLA sharing, and the outcome of treatment for unexplained infertility by in vitro fertilization (IVF) was tested in 76 couples, by using a new shared-allele test in order to identify more precisely the region of the major histocompatibility complex (MHC) influencing these reproductive defects. The shared-allele test circumvents the problem of rare alleles at HLA loci and at the same time provides a substantial gain in power over the simple chi 2 test. Two statistical methods, a corrected homogeneity test and a bootstrap approach, were developed to compare the allele frequencies at each of the HLA-A, HLA-B, HLA-DR, and HLA-DQ loci; they were not statistically different among the three patient groups and the control group. There was a significant excess of HLA-DR sharing in couples with RSA and a significant excess of HLA-DQ sharing in couples with unexplained infertility who failed treatment by IVF. These findings indicate that genes located in different parts of the class II region of the MHC affect different aspects of reproduction and strongly suggest that the sharing of HLA antigens per se is not the mechanism involved in the reproductive defects. The segment of the MHC that has genes affecting reproduction also has genes associated with different autoimmune diseases, and this juxtaposition may explain the association between reproductive defects and autoimmune diseases.
采用一种新的共享等位基因检测方法,对123对夫妇进行了HLA共享与复发性自然流产(RSA)之间关联的检测,并对76对夫妇进行了HLA共享与不明原因不孕症体外受精(IVF)治疗结局之间关联的检测,以便更精确地确定主要组织相容性复合体(MHC)中影响这些生殖缺陷的区域。共享等位基因检测规避了HLA位点罕见等位基因的问题,同时与简单的卡方检验相比,检测效能有显著提高。开发了两种统计方法,即校正齐性检验和自助法,以比较HLA-A、HLA-B、HLA-DR和HLA-DQ各基因座的等位基因频率;在三组患者和对照组中,它们在统计学上没有差异。RSA夫妇中HLA-DR共享显著过量,不明原因不孕症且IVF治疗失败的夫妇中HLA-DQ共享显著过量。这些发现表明,位于MHC II类区域不同部位的基因影响生殖的不同方面,并强烈提示HLA抗原的共享本身并非生殖缺陷所涉及的机制。MHC中影响生殖的基因片段也有与不同自身免疫性疾病相关的基因,这种并列关系可能解释了生殖缺陷与自身免疫性疾病之间的关联。