Lack of the appropriate natural killer cell inhibitory receptors in women with spontaneous abortion

被引:74
作者
Varla-Leftherioti, M
Spyropoulou-Vlachou, M
Keramitsoglou, T
Papadimitropoulos, M
Tsekoura, C
Graphou, O
Papadopoulou, C
Gerondi, A
Stavropoulos-Giokas, CS
机构
[1] Helena Venizelou Matern Hosp, Dept Immunobiol, Athens 11521, Greece
[2] Helena Venizelou Matern Hosp, Dept Perinatal Pathol, Athens, Greece
[3] G Gennimatas Hosp, Dept Immunol, Natl Tissue Typing Ctr, Athens, Greece
关键词
spontaneous abortion; inhibitory KIR receptors;
D O I
10.1016/j.humimm.2004.10.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Previous studies have revealed that women with unexplained recurrent spontaneous abortions have a limited repertoire of inhibitory KI receptors (inhKIRs) and that the inhKIRs they possess do not have specificity for the human leukocyte antigen (HLA)-Cw molecules that would be expressed on trophoblast. We sought to confirm these findings by direct definition of maternal inhKIR and trophoblastic HLA-Cw allotypes on the placental material of spontaneously missed pregnancies. The study included 30 women undergoing vacuum uterine curettage for first-trimester missed pregnancy (group A; n = 15) or for elective termination of normal pregnancy (group C, n = 15). DNA extracted from isolated decidual and trophoblastic cells was used for molecular detection of maternal inhKIRs (2DL1, 2DL2, 2DL3) and fetal HLA-Cw alleles, respectively. The results revealed that in the group of women who experienced abortion, 60% did not have the full repertoire of three inhKIRs (group A vs group C; p = 0.006); that in five of 15 patients (none in the controls), no epitope matching existed between maternal inhKIRs and trophoblastic HLA-Cw alleles (group A vs group C; p = 0.01); and that more cases were found with limited epitope matching (less than three inhKIRs with specificity for fetal HLA-Cw alleles). The results provide additional evidence that in some cases of spontaneous abortions, the women lack the appropriate inhKIRs to interact with the HLA-Cw molecules on trophoblasts and to deliver signals to inhibit natural killer cell activation and protect the embryo. Haman Immunology 66, 65-71 (2005). (C) American Society for Histocompatibility and Immunogenetics, 2005. Published by Elsevier Inc.
引用
收藏
页码:65 / 71
页数:7
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