Nielsen Henriette Svarre, Mogensen Marie, Steffensen Rudi, Kruse Christina, Christiansen Ole Bjarne
The Fertility Clinic 4071, University Hospital Copenhagen, Rigshospitalet, Blegdamsvej 9, DK-2100 Copenhagen, Denmark.
J Reprod Immunol. 2007 Aug;75(1):63-9. doi: 10.1016/j.jri.2007.03.003. Epub 2007 Apr 16.
Placental abruption is a potential life-threatening condition for both the fetus and the mother, being significantly more common in pregnancies with male fetuses. The pathogenesis of placental abruption remains unknown. However, some recent reports point toward a maternal immune response against the fetus as a possible mechanism. No data exist concerning special characteristics of patients suffering recurrent placental abruptions.
Identification of all patients with recurrent placental abruption in a retrospective review of 881 consecutive Caucasian women seen in our tertiary centre for recurrent pregnancy losses between 1986 and 2005. The HLA, DRB1, DRB3, 4, 5 and DQB1 genotypes of patients were compared with relevant controls.
Eight patients were identified with recurrent placental abruption. The patients had a total of 22 abruptions; 18 (82%) in which the fetus died. Seven patients (88%) had first-born boys, and 15 abruptions (68%) involved male fetuses. All patients with a first-born boy, except one, had HLA-class II alleles known to restrict CD4+ T-cell responses against male-specific minor histocompatibility (HY)-antigens (HLA-DRB115, HLA-DRB30301 and HLA-DQB1*05). Haplotypes with these HLA-alleles constituted 64% of the patients' haplotypes compared to 28% of those of the controls (p=0.009). Furthermore, 43% of the patients were homozygous for these haplotypes compared to 5% of controls (p=0.023).
We have found that recurrent placental abruption is exclusively almost preceded by the birth of a boy and the majority of patients have HLA-class II known to restrict CD4 T-cell reactions against HY-antigens. This indicates that maternal immunological responses against HY-antigens play a role in recurrent placental abruption.
胎盘早剥对胎儿和母亲来说都是一种潜在的危及生命的情况,在怀有男性胎儿的妊娠中更为常见。胎盘早剥的发病机制尚不清楚。然而,最近的一些报告指出,母亲对胎儿的免疫反应可能是一种机制。目前尚无关于复发性胎盘早剥患者特殊特征的数据。
在对1986年至2005年间在我们三级中心因复发性流产就诊的881名连续的白种女性进行回顾性研究中,识别出所有复发性胎盘早剥患者。将患者的HLA、DRB1、DRB3、4、5和DQB1基因型与相关对照组进行比较。
识别出8例复发性胎盘早剥患者。这些患者共有22次胎盘早剥;其中18次(82%)胎儿死亡。7例患者(88%)的头胎为男孩,15次胎盘早剥(68%)涉及男性胎儿。除1例患者外,所有头胎为男孩的患者都具有已知可限制CD4+T细胞对男性特异性次要组织相容性(HY)抗原反应的HLA-II类等位基因(HLA-DRB115、HLA-DRB30301和HLA-DQB1*05)。与对照组的28%相比,具有这些HLA等位基因的单倍型占患者单倍型的64%(p=0.009)。此外,43%的患者这些单倍型为纯合子,而对照组为5%(p=0.023)。
我们发现复发性胎盘早剥几乎都发生在男孩出生之后,且大多数患者具有已知可限制CD4 T细胞对HY抗原反应的HLA-II类基因。这表明母亲对HY抗原的免疫反应在复发性胎盘早剥中起作用。