Wang Shan, Zhao Yue-Ran, Jiao Yu-Lian, Wang Lai-Cheng, Li Jian-Feng, Cui Bin, Xu Cheng-Yan, Shi Yu-Hua, Chen Zi-Jiang
Research Center for Reproductive Medicine, Shandong Provincial Hospital of Shandong University, Jinan 250021, China.
Biochem Biophys Res Commun. 2007 Aug 31;360(3):696-701. doi: 10.1016/j.bbrc.2007.06.125. Epub 2007 Jul 2.
Accumulating evidence indicates natural killer (NK) cells play crucial roles in successful pregnancy. To investigate whether the killer cell immunoglobulin-like receptor (KIR) gene polymorphism and the corresponding specific HLA ligands in parent couples possessing a susceptibility to unexplained recurrent spontaneous abortion (RSA), we searched 73 pairs of childless couples with three or more abortions characterized as unexplained RSA and 68 pairs of healthy control couples. Peripheral blood was drawn to obtain genomic DNA which was used for a polymerase chain reaction using sequence-specific primers (PCR-SSP) in order to determine whether 15 selected KIR genes and two groups of HLA-C alleles were present. Our result showed that gene frequency of KIR2DS1 was higher in patients with RSA compared to that of control subjects (P =0.029). Increased numbers of activating KIR genes was observed in patients (P =0.041). Women who possessed more than two activating KIR genes were found more frequently in patients than those in control subjects (P =0.018). From a cohort of husband and wife couples, the women with a KIR2DS1 gene, and with a decreased group 2 HLA-C allele for the homologous inhibitory receptor KIR2DL1, had a tendency to fall into the RSA group (P =0.004). The results suggest that a genetic variation at the KIR locus influences the susceptibility to unexplained RSA in the Chinese Han population. Moreover, decreased ligands for inhibitory KIRs could potentially lower the threshold for NK cell activation, mediated through activating receptors, thereby contributing to pathogenesis of RSA.
越来越多的证据表明,自然杀伤(NK)细胞在成功妊娠中起着至关重要的作用。为了研究在患有不明原因复发性自然流产(RSA)易感性的夫妇中,杀伤细胞免疫球蛋白样受体(KIR)基因多态性及相应的特异性HLA配体情况,我们对73对有三次或更多次流产且被判定为不明原因RSA的未育夫妇以及68对健康对照夫妇进行了研究。采集外周血以获取基因组DNA,使用序列特异性引物的聚合酶链反应(PCR-SSP)来确定15个选定的KIR基因和两组HLA-C等位基因是否存在。我们的结果显示,与对照组相比,RSA患者中KIR2DS1的基因频率更高(P = 0.029)。在患者中观察到激活型KIR基因数量增加(P = 0.041)。拥有两个以上激活型KIR基因的女性在患者中比对照组更常见(P = 0.018)。在夫妻队列中,携带KIR2DS1基因且同源抑制性受体KIR2DL1的第2组HLA-C等位基因减少的女性有进入RSA组的倾向(P = 0.004)。结果表明,KIR基因座的遗传变异影响中国汉族人群对不明原因RSA的易感性。此外,抑制性KIRs的配体减少可能会通过激活受体潜在地降低NK细胞激活的阈值,从而导致RSA的发病机制。